Stojić-Vukanić, Zorica

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  • Stojić-Vukanić, Zorica (75)

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Ageing Affects Thymopoiesis and Experimental Autoimmune Encephalomyelitis Development in a Strain-Dependent Manner

Stojić-Vukanić, Zorica; Petrušić, Marija; Pilipović, Ivan; Leposavić, Gordana

(S. Karger AG, Basel., 2023)

TY  - JOUR
AU  - Stojić-Vukanić, Zorica
AU  - Petrušić, Marija
AU  - Pilipović, Ivan
AU  - Leposavić, Gordana
PY  - 2023
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/5411
AB  - INTRODUCTION: Considering significance of mechanisms of central tolerance for development of autoimmune diseases, including experimental autoimmune encephalomyelitis (EAE), and suppressive influence of circulating proinflammatory cytokines and alterations in brain-thymus communication, characteristic for the central nervous system (CNS) autoimmune diseases, on thymopoiesis, the study interogated putative strain-based thymus-related specificities relevant for the opposite effects of ageing on susceptibility of Dark Agouti (DA) and Albino Oxford (AO) rats to EAE. METHODS: Quantitative and qualitative changes in thymopoiesis including underlying mechanisms were examined using flow cytometry and RT-qPCR quantification of mRNAs for molecules relevant for integrity of stroma and T-cell development, respectively. RESULTS: With ageing, differently from DA rats, in AO rats the surface density of CD90, a negative regulator of selection threshold, on thymocytes undergoing lineage commitment was upregulated (consistent with TGF-β expression downregulation), whereas the generation of natural CD4+CD25+Foxp3+ regulatory T cells (nTregs) was impaired reflecting differences in thymic expression of cytokines supporting their development. Additionally, specifically in old AO rats, in whom EAE development depends on IL-17-producing CD8+ T cells, their thymic differentiation was augmented, reflecting augmented thymic IL-4 expression. In turn, differently from old DA rats developing self-limiting EAE, in age-matched AO rats developing EAE of prolonged duration, EAE development led to impaired generation of nTregs and accumulation of proinflammatory, cytotoxic CD28-CD4+ T cells in the periphery. DISCUSSION: The study indicates that strain differences in age-related changes in the efficacy of central tolerance, in addition to enhanced thymic generation of CD8+ T cells prone to differentiate into IL-17-producing cells, could partly explain the opposite effect of ageing on DA and AO rat susceptibility to EAE induction. Additionally, it suggested that EAE development leading to a less efficient thymic output of CD4+ cells and nTregs in old AO rats than their DA counterparts could contribute to prolonged EAE duration in AO compared with DA rats. CONCLUSION: The study warns to caution when designing therapeutic interventions to enhance thymic activity in genetically diverse populations, e.g., humans, and interpreting their outcomes. Furthermore, it indicates that CNS autoimmune pathology may additionally worsen thymic involution and age-related immune changes.
PB  - S. Karger AG, Basel.
T2  - Neuroimmunomodulation
T1  - Ageing Affects Thymopoiesis and Experimental Autoimmune Encephalomyelitis Development in a Strain-Dependent Manner
VL  - 30
IS  - 1
SP  - 346
EP  - 373
DO  - 10.1159/000535150
ER  - 
@article{
author = "Stojić-Vukanić, Zorica and Petrušić, Marija and Pilipović, Ivan and Leposavić, Gordana",
year = "2023",
abstract = "INTRODUCTION: Considering significance of mechanisms of central tolerance for development of autoimmune diseases, including experimental autoimmune encephalomyelitis (EAE), and suppressive influence of circulating proinflammatory cytokines and alterations in brain-thymus communication, characteristic for the central nervous system (CNS) autoimmune diseases, on thymopoiesis, the study interogated putative strain-based thymus-related specificities relevant for the opposite effects of ageing on susceptibility of Dark Agouti (DA) and Albino Oxford (AO) rats to EAE. METHODS: Quantitative and qualitative changes in thymopoiesis including underlying mechanisms were examined using flow cytometry and RT-qPCR quantification of mRNAs for molecules relevant for integrity of stroma and T-cell development, respectively. RESULTS: With ageing, differently from DA rats, in AO rats the surface density of CD90, a negative regulator of selection threshold, on thymocytes undergoing lineage commitment was upregulated (consistent with TGF-β expression downregulation), whereas the generation of natural CD4+CD25+Foxp3+ regulatory T cells (nTregs) was impaired reflecting differences in thymic expression of cytokines supporting their development. Additionally, specifically in old AO rats, in whom EAE development depends on IL-17-producing CD8+ T cells, their thymic differentiation was augmented, reflecting augmented thymic IL-4 expression. In turn, differently from old DA rats developing self-limiting EAE, in age-matched AO rats developing EAE of prolonged duration, EAE development led to impaired generation of nTregs and accumulation of proinflammatory, cytotoxic CD28-CD4+ T cells in the periphery. DISCUSSION: The study indicates that strain differences in age-related changes in the efficacy of central tolerance, in addition to enhanced thymic generation of CD8+ T cells prone to differentiate into IL-17-producing cells, could partly explain the opposite effect of ageing on DA and AO rat susceptibility to EAE induction. Additionally, it suggested that EAE development leading to a less efficient thymic output of CD4+ cells and nTregs in old AO rats than their DA counterparts could contribute to prolonged EAE duration in AO compared with DA rats. CONCLUSION: The study warns to caution when designing therapeutic interventions to enhance thymic activity in genetically diverse populations, e.g., humans, and interpreting their outcomes. Furthermore, it indicates that CNS autoimmune pathology may additionally worsen thymic involution and age-related immune changes.",
publisher = "S. Karger AG, Basel.",
journal = "Neuroimmunomodulation",
title = "Ageing Affects Thymopoiesis and Experimental Autoimmune Encephalomyelitis Development in a Strain-Dependent Manner",
volume = "30",
number = "1",
pages = "346-373",
doi = "10.1159/000535150"
}
Stojić-Vukanić, Z., Petrušić, M., Pilipović, I.,& Leposavić, G.. (2023). Ageing Affects Thymopoiesis and Experimental Autoimmune Encephalomyelitis Development in a Strain-Dependent Manner. in Neuroimmunomodulation
S. Karger AG, Basel.., 30(1), 346-373.
https://doi.org/10.1159/000535150
Stojić-Vukanić Z, Petrušić M, Pilipović I, Leposavić G. Ageing Affects Thymopoiesis and Experimental Autoimmune Encephalomyelitis Development in a Strain-Dependent Manner. in Neuroimmunomodulation. 2023;30(1):346-373.
doi:10.1159/000535150 .
Stojić-Vukanić, Zorica, Petrušić, Marija, Pilipović, Ivan, Leposavić, Gordana, "Ageing Affects Thymopoiesis and Experimental Autoimmune Encephalomyelitis Development in a Strain-Dependent Manner" in Neuroimmunomodulation, 30, no. 1 (2023):346-373,
https://doi.org/10.1159/000535150 . .

Nanoparticle-Based Adjuvants and Delivery Systems for Modern Vaccines

Filipić, Brankica; Pantelić, Ivana; Nikolić, Ines; Majhen, Dragomira; Stojić-Vukanić, Zorica; Savić, Snežana; Krajišnik, Danina

(MDPI, 2023)

TY  - JOUR
AU  - Filipić, Brankica
AU  - Pantelić, Ivana
AU  - Nikolić, Ines
AU  - Majhen, Dragomira
AU  - Stojić-Vukanić, Zorica
AU  - Savić, Snežana
AU  - Krajišnik, Danina
PY  - 2023
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/4960
AB  - Ever since the development of the first vaccine, vaccination has had the great impact on global health, leading to the decrease in the burden of numerous infectious diseases. However, there is a constant need to improve existing vaccines and develop new vaccination strategies and vaccine platforms that induce a broader immune response compared to traditional vaccines. Modern vaccines tend to rely on certain nanotechnology platforms but are still expected to be readily available and easy for large-scale manufacturing and to induce a durable immune response. In this review, we present an overview of the most promising nanoadjuvants and nanoparticulate delivery systems and discuss their benefits from tehchnological and immunological standpoints as well as their objective drawbacks and possible side effects. The presented nano alums, silica and clay nanoparticles, nanoemulsions, adenoviral-vectored systems, adeno-associated viral vectors, vesicular stomatitis viral vectors, lentiviral vectors, virus-like particles (including bacteriophage-based ones) and virosomes indicate that vaccine developers can now choose different adjuvants and/or delivery systems as per the requirement, specific to combatting different infectious diseases.
PB  - MDPI
T2  - Vaccines
T1  - Nanoparticle-Based Adjuvants and Delivery Systems for Modern Vaccines
VL  - 11
IS  - 7
DO  - 10.3390/vaccines11071172
ER  - 
@article{
author = "Filipić, Brankica and Pantelić, Ivana and Nikolić, Ines and Majhen, Dragomira and Stojić-Vukanić, Zorica and Savić, Snežana and Krajišnik, Danina",
year = "2023",
abstract = "Ever since the development of the first vaccine, vaccination has had the great impact on global health, leading to the decrease in the burden of numerous infectious diseases. However, there is a constant need to improve existing vaccines and develop new vaccination strategies and vaccine platforms that induce a broader immune response compared to traditional vaccines. Modern vaccines tend to rely on certain nanotechnology platforms but are still expected to be readily available and easy for large-scale manufacturing and to induce a durable immune response. In this review, we present an overview of the most promising nanoadjuvants and nanoparticulate delivery systems and discuss their benefits from tehchnological and immunological standpoints as well as their objective drawbacks and possible side effects. The presented nano alums, silica and clay nanoparticles, nanoemulsions, adenoviral-vectored systems, adeno-associated viral vectors, vesicular stomatitis viral vectors, lentiviral vectors, virus-like particles (including bacteriophage-based ones) and virosomes indicate that vaccine developers can now choose different adjuvants and/or delivery systems as per the requirement, specific to combatting different infectious diseases.",
publisher = "MDPI",
journal = "Vaccines",
title = "Nanoparticle-Based Adjuvants and Delivery Systems for Modern Vaccines",
volume = "11",
number = "7",
doi = "10.3390/vaccines11071172"
}
Filipić, B., Pantelić, I., Nikolić, I., Majhen, D., Stojić-Vukanić, Z., Savić, S.,& Krajišnik, D.. (2023). Nanoparticle-Based Adjuvants and Delivery Systems for Modern Vaccines. in Vaccines
MDPI., 11(7).
https://doi.org/10.3390/vaccines11071172
Filipić B, Pantelić I, Nikolić I, Majhen D, Stojić-Vukanić Z, Savić S, Krajišnik D. Nanoparticle-Based Adjuvants and Delivery Systems for Modern Vaccines. in Vaccines. 2023;11(7).
doi:10.3390/vaccines11071172 .
Filipić, Brankica, Pantelić, Ivana, Nikolić, Ines, Majhen, Dragomira, Stojić-Vukanić, Zorica, Savić, Snežana, Krajišnik, Danina, "Nanoparticle-Based Adjuvants and Delivery Systems for Modern Vaccines" in Vaccines, 11, no. 7 (2023),
https://doi.org/10.3390/vaccines11071172 . .
5
5

Adrenoceptors as potential target for add-on immunomodulatory therapy in multiple sclerosis

Pilipović, Ivan; Stojić-Vukanić, Zorica; Leposavić, Gordana

(Elsevier Inc., 2023)

TY  - JOUR
AU  - Pilipović, Ivan
AU  - Stojić-Vukanić, Zorica
AU  - Leposavić, Gordana
PY  - 2023
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/4470
AB  - This review summarizes recent findings related to the role of the sympathetic nervous system (SNS) in pathogenesis of multiple sclerosis (MS) and its commonly used experimental model – experimental autoimmune encephalomyelitis (EAE). They indicate that noradrenaline, the key end-point mediator of the SNS, acting through β-adrenoceptor, has a contributory role in the early stages of MS/EAE development. This stage is characterized by the SNS hyperactivity (increased release of noradrenaline) reflecting the net effect of different factors, such as the disease-associated inflammation, stress, vitamin D hypovitaminosis, Epstein-Barr virus infection and dysbiosis. Thus, the administration of propranolol, a non-selective β-adrenoceptor blocker, readily crossing the blood-brain barrier, to experimental rats before the autoimmune challenge and in the early (preclinical/prodromal) phase of the disease mitigates EAE severity. This phenomenon has been ascribed to the alleviation of neuroinflammation (due to attenuation of primarily microglial activation/proinflammatory functions) and the diminution of the magnitude of the primary CD4+ T-cell autoimmune response (the effect associated with impaired autoantigen uptake by antigen presenting cells and their migration into draining lymph nodes). The former is partly related to breaking of the catecholamine-dependent self-amplifying microglial feed-forward loop and the positive feedback loop between microglia and the SNS, leading to down-regulation of the SNS hyperactivity and its enhancing influence on microglial activation/proinflammatory functions and the magnitude of autoimmune response. The effects of propranolol are shown to be more prominent in male EAE animals, the phenomenon important as males (like men) are likely to develop clinically more severe disease. Thus, these findings could serve as a firm scientific background for formulation of a new sex-specific immune-intervention strategy for the early phases of MS (characterized by the SNS hyperactivity) exploiting anti-(neuro)inflammatory and immunomodulatory properties of propranolol and other relatively cheap and safe adrenergic drugs with similar therapeutic profile.
PB  - Elsevier Inc.
T2  - Pharmacology and Therapeutics
T1  - Adrenoceptors as potential target for add-on immunomodulatory therapy in multiple sclerosis
VL  - 243
DO  - 10.1016/j.pharmthera.2023.108358
ER  - 
@article{
author = "Pilipović, Ivan and Stojić-Vukanić, Zorica and Leposavić, Gordana",
year = "2023",
abstract = "This review summarizes recent findings related to the role of the sympathetic nervous system (SNS) in pathogenesis of multiple sclerosis (MS) and its commonly used experimental model – experimental autoimmune encephalomyelitis (EAE). They indicate that noradrenaline, the key end-point mediator of the SNS, acting through β-adrenoceptor, has a contributory role in the early stages of MS/EAE development. This stage is characterized by the SNS hyperactivity (increased release of noradrenaline) reflecting the net effect of different factors, such as the disease-associated inflammation, stress, vitamin D hypovitaminosis, Epstein-Barr virus infection and dysbiosis. Thus, the administration of propranolol, a non-selective β-adrenoceptor blocker, readily crossing the blood-brain barrier, to experimental rats before the autoimmune challenge and in the early (preclinical/prodromal) phase of the disease mitigates EAE severity. This phenomenon has been ascribed to the alleviation of neuroinflammation (due to attenuation of primarily microglial activation/proinflammatory functions) and the diminution of the magnitude of the primary CD4+ T-cell autoimmune response (the effect associated with impaired autoantigen uptake by antigen presenting cells and their migration into draining lymph nodes). The former is partly related to breaking of the catecholamine-dependent self-amplifying microglial feed-forward loop and the positive feedback loop between microglia and the SNS, leading to down-regulation of the SNS hyperactivity and its enhancing influence on microglial activation/proinflammatory functions and the magnitude of autoimmune response. The effects of propranolol are shown to be more prominent in male EAE animals, the phenomenon important as males (like men) are likely to develop clinically more severe disease. Thus, these findings could serve as a firm scientific background for formulation of a new sex-specific immune-intervention strategy for the early phases of MS (characterized by the SNS hyperactivity) exploiting anti-(neuro)inflammatory and immunomodulatory properties of propranolol and other relatively cheap and safe adrenergic drugs with similar therapeutic profile.",
publisher = "Elsevier Inc.",
journal = "Pharmacology and Therapeutics",
title = "Adrenoceptors as potential target for add-on immunomodulatory therapy in multiple sclerosis",
volume = "243",
doi = "10.1016/j.pharmthera.2023.108358"
}
Pilipović, I., Stojić-Vukanić, Z.,& Leposavić, G.. (2023). Adrenoceptors as potential target for add-on immunomodulatory therapy in multiple sclerosis. in Pharmacology and Therapeutics
Elsevier Inc.., 243.
https://doi.org/10.1016/j.pharmthera.2023.108358
Pilipović I, Stojić-Vukanić Z, Leposavić G. Adrenoceptors as potential target for add-on immunomodulatory therapy in multiple sclerosis. in Pharmacology and Therapeutics. 2023;243.
doi:10.1016/j.pharmthera.2023.108358 .
Pilipović, Ivan, Stojić-Vukanić, Zorica, Leposavić, Gordana, "Adrenoceptors as potential target for add-on immunomodulatory therapy in multiple sclerosis" in Pharmacology and Therapeutics, 243 (2023),
https://doi.org/10.1016/j.pharmthera.2023.108358 . .
2
3
2

Thymic changes as a contributing factor in the increased susceptibility of old Albino Oxford rats to EAE development

Petrušić, Marija; Stojić-Vukanić, Zorica; Pilipović, Ivan; Kosec, Duško; Prijić, Ivana; Leposavić, Gordana

(Elsevier Inc., 2023)

TY  - JOUR
AU  - Petrušić, Marija
AU  - Stojić-Vukanić, Zorica
AU  - Pilipović, Ivan
AU  - Kosec, Duško
AU  - Prijić, Ivana
AU  - Leposavić, Gordana
PY  - 2023
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/4316
AB  - The study was aimed to examine putative contribution of thymic involution to ageing-associated increase in susceptibility of Albino Oxford (AO) rats to the development of clinical EAE, and vice versa influence of the disease on the progression of thymic involution. To this end we examined (i) the parameters of thymocyte negative selection efficacy, the thymic generation of CD4+CD25+Foxp3+ T regulatory cells (Tregs) and thymic capacity to instruct/predetermine IL-17-producing T-cell differentiation, and thymopietic efficacy-associated accumulation of “inflammescent” cytotoxic CD28- T cells in the periphery, and (ii) the key underlying mechanisms in young and old non-immunised AO rats and their counterparts immunised for EAE (on the 16th day post-immunisation when the disease in old rats reached the plateau) using flow cytometry analysis and/or RT-qPCR. It was found that thymic involution impairs: (i) the efficacy of negative selection (by affecting thymocyte expression of CD90, negative regulator of selection threshold and the expression of thymic stromal cell integrity factors) and (ii) Treg generation (by diminishing expression of cytokines supporting their differentiation/maturation). Additionally, the results suggest that thymic involution facilitates CD8+ T-cell differentiation into IL-17-producing cells (previously linked to the development of clinical EAE in old AO rats). Furthermore, they confirmed that ageing-related decrease in thymic T-cell output (as indicated by diminished frequency of recent thymic emigrants in peripheral blood) resulted in the accumulation of CD28- T cells in peripheral blood and, upon immunisation, in the target organ. On the other hand, the development of EAE (most likely by increasing circulatory levels of proinflammatory cytokines) contributed to the decline in thymic output of T cells, including Tregs, and thereby to the progression/maintenance of clinical EAE. Thus, in AO rats thymic involution via multi-layered mechanisms may favour the development of clinically manifested autoimmunity, which, in turn, precipitates the thymus atrophy.
PB  - Elsevier Inc.
T2  - Experimental Gerontology
T1  - Thymic changes as a contributing factor in the increased susceptibility of old Albino Oxford rats to EAE development
VL  - 171
DO  - 10.1016/j.exger.2022.112009
ER  - 
@article{
author = "Petrušić, Marija and Stojić-Vukanić, Zorica and Pilipović, Ivan and Kosec, Duško and Prijić, Ivana and Leposavić, Gordana",
year = "2023",
abstract = "The study was aimed to examine putative contribution of thymic involution to ageing-associated increase in susceptibility of Albino Oxford (AO) rats to the development of clinical EAE, and vice versa influence of the disease on the progression of thymic involution. To this end we examined (i) the parameters of thymocyte negative selection efficacy, the thymic generation of CD4+CD25+Foxp3+ T regulatory cells (Tregs) and thymic capacity to instruct/predetermine IL-17-producing T-cell differentiation, and thymopietic efficacy-associated accumulation of “inflammescent” cytotoxic CD28- T cells in the periphery, and (ii) the key underlying mechanisms in young and old non-immunised AO rats and their counterparts immunised for EAE (on the 16th day post-immunisation when the disease in old rats reached the plateau) using flow cytometry analysis and/or RT-qPCR. It was found that thymic involution impairs: (i) the efficacy of negative selection (by affecting thymocyte expression of CD90, negative regulator of selection threshold and the expression of thymic stromal cell integrity factors) and (ii) Treg generation (by diminishing expression of cytokines supporting their differentiation/maturation). Additionally, the results suggest that thymic involution facilitates CD8+ T-cell differentiation into IL-17-producing cells (previously linked to the development of clinical EAE in old AO rats). Furthermore, they confirmed that ageing-related decrease in thymic T-cell output (as indicated by diminished frequency of recent thymic emigrants in peripheral blood) resulted in the accumulation of CD28- T cells in peripheral blood and, upon immunisation, in the target organ. On the other hand, the development of EAE (most likely by increasing circulatory levels of proinflammatory cytokines) contributed to the decline in thymic output of T cells, including Tregs, and thereby to the progression/maintenance of clinical EAE. Thus, in AO rats thymic involution via multi-layered mechanisms may favour the development of clinically manifested autoimmunity, which, in turn, precipitates the thymus atrophy.",
publisher = "Elsevier Inc.",
journal = "Experimental Gerontology",
title = "Thymic changes as a contributing factor in the increased susceptibility of old Albino Oxford rats to EAE development",
volume = "171",
doi = "10.1016/j.exger.2022.112009"
}
Petrušić, M., Stojić-Vukanić, Z., Pilipović, I., Kosec, D., Prijić, I.,& Leposavić, G.. (2023). Thymic changes as a contributing factor in the increased susceptibility of old Albino Oxford rats to EAE development. in Experimental Gerontology
Elsevier Inc.., 171.
https://doi.org/10.1016/j.exger.2022.112009
Petrušić M, Stojić-Vukanić Z, Pilipović I, Kosec D, Prijić I, Leposavić G. Thymic changes as a contributing factor in the increased susceptibility of old Albino Oxford rats to EAE development. in Experimental Gerontology. 2023;171.
doi:10.1016/j.exger.2022.112009 .
Petrušić, Marija, Stojić-Vukanić, Zorica, Pilipović, Ivan, Kosec, Duško, Prijić, Ivana, Leposavić, Gordana, "Thymic changes as a contributing factor in the increased susceptibility of old Albino Oxford rats to EAE development" in Experimental Gerontology, 171 (2023),
https://doi.org/10.1016/j.exger.2022.112009 . .
2
2

β-Adrenoceptor Blockade Moderates Neuroinflammation in Male and Female EAE Rats and Abrogates Sexual Dimorphisms in the Major Neuroinflammatory Pathways by Being More Efficient in Males

Pilipović, Ivan; Stojić-Vukanić, Zorica; Prijić, Ivana; Jasnić, Nebojša; Đorđević, Jelena; Leposavić, Gordana

(Springer, 2022)

TY  - JOUR
AU  - Pilipović, Ivan
AU  - Stojić-Vukanić, Zorica
AU  - Prijić, Ivana
AU  - Jasnić, Nebojša
AU  - Đorđević, Jelena
AU  - Leposavić, Gordana
PY  - 2022
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/4198
AB  - Our previous studies showed more severe experimental autoimmune encephalomyelitis (EAE) in male compared with female adult rats, and moderating effect of propranolol-induced β-adrenoceptor blockade on EAE in females, the effect associated with transcriptional stimulation of Nrf2/HO-1 axis in spinal cord microglia. This study examined putative sexual dimor- phism in propranolol action on EAE severity. Propranolol treatment beginning from the onset of clinical EAE mitigated EAE severity in rats of both sexes, but to a greater extent in males exhibiting higher noradrenaline levels and myeloid cell β 2 -adrenoceptor expression in spinal cord. This correlated with more prominent stimulatory effects of propranolol not only on CX3CL1/CX3CR1/Nrf2/HO-1 cascade, but also on Stat3/Socs3 signaling axis in spinal cord microglia/myeloid cells (mirrored in the decreased Stat3 and the increased Socs3 expression) from male rats compared with their female counterparts. Propranolol diminished the frequency of activated cells among microglia, increased their phagocyting/endocyting capacity, and shifted cytokine secretory profile of microglia/blood-borne myeloid cells towards an anti-inflammatory/neuroprotective phenotype. Additionally, it downregulated the expression of chemokines (CCL2, CCL19/21) driving T-cell/monocyte traf- ficking into spinal cord. Consequently, in propranolol-treated rats fewer activated CD4+ T cells and IL-17+ T cells, including CD4+IL17+ cells coexpressing IFN-γ/GM-CSF, were recovered from spinal cord of propranolol-treated rats compared with sex-matched saline-injected controls. All the effects of propranolol were more prominent in males. The study as a whole disclosed that sexual dimorphism in multiple molecular mechanisms implicated in EAE development may be responsible for greater severity of EAE in male rats and sexually dimorphic action of substances affecting them.
PB  - Springer
T2  - Cellular and Molecular Neurobiology
T1  - β-Adrenoceptor Blockade Moderates Neuroinflammation in Male and Female EAE Rats and Abrogates Sexual Dimorphisms in the Major Neuroinflammatory Pathways by Being More Efficient in Males
DO  - 10.1007/s10571-022-01246-z
ER  - 
@article{
author = "Pilipović, Ivan and Stojić-Vukanić, Zorica and Prijić, Ivana and Jasnić, Nebojša and Đorđević, Jelena and Leposavić, Gordana",
year = "2022",
abstract = "Our previous studies showed more severe experimental autoimmune encephalomyelitis (EAE) in male compared with female adult rats, and moderating effect of propranolol-induced β-adrenoceptor blockade on EAE in females, the effect associated with transcriptional stimulation of Nrf2/HO-1 axis in spinal cord microglia. This study examined putative sexual dimor- phism in propranolol action on EAE severity. Propranolol treatment beginning from the onset of clinical EAE mitigated EAE severity in rats of both sexes, but to a greater extent in males exhibiting higher noradrenaline levels and myeloid cell β 2 -adrenoceptor expression in spinal cord. This correlated with more prominent stimulatory effects of propranolol not only on CX3CL1/CX3CR1/Nrf2/HO-1 cascade, but also on Stat3/Socs3 signaling axis in spinal cord microglia/myeloid cells (mirrored in the decreased Stat3 and the increased Socs3 expression) from male rats compared with their female counterparts. Propranolol diminished the frequency of activated cells among microglia, increased their phagocyting/endocyting capacity, and shifted cytokine secretory profile of microglia/blood-borne myeloid cells towards an anti-inflammatory/neuroprotective phenotype. Additionally, it downregulated the expression of chemokines (CCL2, CCL19/21) driving T-cell/monocyte traf- ficking into spinal cord. Consequently, in propranolol-treated rats fewer activated CD4+ T cells and IL-17+ T cells, including CD4+IL17+ cells coexpressing IFN-γ/GM-CSF, were recovered from spinal cord of propranolol-treated rats compared with sex-matched saline-injected controls. All the effects of propranolol were more prominent in males. The study as a whole disclosed that sexual dimorphism in multiple molecular mechanisms implicated in EAE development may be responsible for greater severity of EAE in male rats and sexually dimorphic action of substances affecting them.",
publisher = "Springer",
journal = "Cellular and Molecular Neurobiology",
title = "β-Adrenoceptor Blockade Moderates Neuroinflammation in Male and Female EAE Rats and Abrogates Sexual Dimorphisms in the Major Neuroinflammatory Pathways by Being More Efficient in Males",
doi = "10.1007/s10571-022-01246-z"
}
Pilipović, I., Stojić-Vukanić, Z., Prijić, I., Jasnić, N., Đorđević, J.,& Leposavić, G.. (2022). β-Adrenoceptor Blockade Moderates Neuroinflammation in Male and Female EAE Rats and Abrogates Sexual Dimorphisms in the Major Neuroinflammatory Pathways by Being More Efficient in Males. in Cellular and Molecular Neurobiology
Springer..
https://doi.org/10.1007/s10571-022-01246-z
Pilipović I, Stojić-Vukanić Z, Prijić I, Jasnić N, Đorđević J, Leposavić G. β-Adrenoceptor Blockade Moderates Neuroinflammation in Male and Female EAE Rats and Abrogates Sexual Dimorphisms in the Major Neuroinflammatory Pathways by Being More Efficient in Males. in Cellular and Molecular Neurobiology. 2022;.
doi:10.1007/s10571-022-01246-z .
Pilipović, Ivan, Stojić-Vukanić, Zorica, Prijić, Ivana, Jasnić, Nebojša, Đorđević, Jelena, Leposavić, Gordana, "β-Adrenoceptor Blockade Moderates Neuroinflammation in Male and Female EAE Rats and Abrogates Sexual Dimorphisms in the Major Neuroinflammatory Pathways by Being More Efficient in Males" in Cellular and Molecular Neurobiology (2022),
https://doi.org/10.1007/s10571-022-01246-z . .
3
2

Alterations in hemopoiesis in old albino oxford rats contribute to their increased susceptibility to EAE

Petrušić, Marija; Stojić-Vukanić, Zorica; Pilipović, Ivan; Leposavić, Gordana

(Wiley-VCH GmbH, 2022)

TY  - CONF
AU  - Petrušić, Marija
AU  - Stojić-Vukanić, Zorica
AU  - Pilipović, Ivan
AU  - Leposavić, Gordana
PY  - 2022
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/5088
AB  - Multiple studies reveal differences in the phenotype and function of tolerogenic dendritic cells (tolDCs) depending on a tolerizing compound used during DC induction towards tolDCs. ...
PB  - Wiley-VCH GmbH
C3  - European Journal of Immunology
T1  - Alterations in hemopoiesis in old albino oxford rats contribute  to their increased susceptibility to EAE
VL  - 52
IS  - Suppl. 2
SP  - 103
EP  - 103
DO  - 10.1002/eji.202270200
ER  - 
@conference{
author = "Petrušić, Marija and Stojić-Vukanić, Zorica and Pilipović, Ivan and Leposavić, Gordana",
year = "2022",
abstract = "Multiple studies reveal differences in the phenotype and function of tolerogenic dendritic cells (tolDCs) depending on a tolerizing compound used during DC induction towards tolDCs. ...",
publisher = "Wiley-VCH GmbH",
journal = "European Journal of Immunology",
title = "Alterations in hemopoiesis in old albino oxford rats contribute  to their increased susceptibility to EAE",
volume = "52",
number = "Suppl. 2",
pages = "103-103",
doi = "10.1002/eji.202270200"
}
Petrušić, M., Stojić-Vukanić, Z., Pilipović, I.,& Leposavić, G.. (2022). Alterations in hemopoiesis in old albino oxford rats contribute  to their increased susceptibility to EAE. in European Journal of Immunology
Wiley-VCH GmbH., 52(Suppl. 2), 103-103.
https://doi.org/10.1002/eji.202270200
Petrušić M, Stojić-Vukanić Z, Pilipović I, Leposavić G. Alterations in hemopoiesis in old albino oxford rats contribute  to their increased susceptibility to EAE. in European Journal of Immunology. 2022;52(Suppl. 2):103-103.
doi:10.1002/eji.202270200 .
Petrušić, Marija, Stojić-Vukanić, Zorica, Pilipović, Ivan, Leposavić, Gordana, "Alterations in hemopoiesis in old albino oxford rats contribute  to their increased susceptibility to EAE" in European Journal of Immunology, 52, no. Suppl. 2 (2022):103-103,
https://doi.org/10.1002/eji.202270200 . .
6

Future perspectives of therapeutic monoclonal antibodies development: new formats and new functions

Stojić-Vukanić, Zorica

(Savez farmaceutskih udruženja Srbije (SFUS), 2022)

TY  - CONF
AU  - Stojić-Vukanić, Zorica
PY  - 2022
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/4441
AB  - Monoclonal antibody therapeutics have dramatically changed the landscape of
medicine and human health. In 2022, thirty-six years on from the approval of a first
monoclonal antibody, about 100 monoclonal antibodies for treatment of cancer and
noncancer indications had secured United States Food and Drug Administration approval.
The idea that antibodies could serve as therapeutics emerged over century ago, but it
became a reality when scientists developed hybridoma technology for antibody generation
in the laboratory. To avoid the shortcomings of the earliest therapeutic monoclonal
antibodies of murine origin, which tended to be immunogenic in humans, therapeutic
antibody constructs that were more human-compatible (chimeric and humanized) have been
produced using genetic engineering technology. Finally, development of phage display, the
human antibody mouse, and single B cell antibody innovative technologies, have enabled
production of fully human therapeutic antibodies. The successful application of full-size
monoclonal antibodies over the last decades has motivated the pharmaceutical company to
develop various types of antibody formats in order to improve their efficacy and lower
adverse effects. By using strategies to miniaturize and multifunctionalize antibody molecules
new classes of antibody therapeutics, such as antibody derivatives (e.g., antibody–drug
conjugates and immunocytokines), bispecific/multispecific antibodies, antibody fragments,
were developed. In the future, with the progress of modern biotechnology, it can be expected
that these new-designed antibodies will finally pave the way for successful treatments of
various diseases.
AB  - Otkriće monoklonskih antitela i njihova primena u terapiji je značajno uticala na
lečenje i zdravlje ljudi širom sveta. Danas, tri i po decenije nakon što je prvo monoklonsko
antitelo odobreno za upotrebu od strane Agencije za hranu i lekove Sjedinjenih Američkih
Država, više od 100 ovih terapeutika za lečenje malignih tumora i drugih bolesti se nalazi na
tržištu. Iako je ideja da se antitela mogu koristiti kao lekovi stara više od jednog veka, do
njene realizacije je došlo tek kada su naučnici uspostavili tehnologiju za dobijanje hibridoma
ćelija čime je bila omogućena proizvodnja antitela u laboratorijskim uslovima. S obzirom da
su ta prva terapijska antitela bila mišja i samim tim imunogena za čoveka, razvojem
tehnologije genetskog inženjeringa omogućeno je konstruisanje antitela koja su više
“humana” (tzv. himerna i humanizovana). Konačno, uspostavljanjem inovativnih platformi za
prikazivanje antitela ili njihovih fragmenata na fagima (“phage display”), generisanje miševa
koji sintetišu humana antitela ili izolaciju gena za antitela iz pojedinačne B ćelije omogućeno
je dobijanje potpuno humanih antitela. I pored više nego uspešne primene celih molekula
antitela u terapiji, da bi se prevazišla nedovoljna efikasnost nekih od njih i smanjili neželjeni
efekti, farmaceutske kompanije su počele da razvijaju različite formate antitela. Korišćenjem
strategije smanjenja veličine i/ili povećanja funkcionalnosti molekula antitela razvijena je
potpuno nova klasa terapijskih antitela kao što su derivati antitela (npr. konjugati antitela i
lekova), bispecifična/multispecifična antitela, fragmenti antitela i drugi. U budućnosti, sa
daljim razvojem moderne biotehnologije, može se očekivati da će ta novodizajnirana antitela
omogućiti uspešno lečenje mnogih bolesti.
PB  - Savez farmaceutskih udruženja Srbije (SFUS)
C3  - Arhiv za farmaciju
T1  - Future perspectives of therapeutic monoclonal antibodies development: new formats and new functions
T1  - Dalji pravci razvoja terapijskih monoklonskih antitela: novi formati i nove funkcije
VL  - 72
IS  - 4 suplement
SP  - S35
EP  - S36
UR  - https://hdl.handle.net/21.15107/rcub_farfar_4441
ER  - 
@conference{
author = "Stojić-Vukanić, Zorica",
year = "2022",
abstract = "Monoclonal antibody therapeutics have dramatically changed the landscape of
medicine and human health. In 2022, thirty-six years on from the approval of a first
monoclonal antibody, about 100 monoclonal antibodies for treatment of cancer and
noncancer indications had secured United States Food and Drug Administration approval.
The idea that antibodies could serve as therapeutics emerged over century ago, but it
became a reality when scientists developed hybridoma technology for antibody generation
in the laboratory. To avoid the shortcomings of the earliest therapeutic monoclonal
antibodies of murine origin, which tended to be immunogenic in humans, therapeutic
antibody constructs that were more human-compatible (chimeric and humanized) have been
produced using genetic engineering technology. Finally, development of phage display, the
human antibody mouse, and single B cell antibody innovative technologies, have enabled
production of fully human therapeutic antibodies. The successful application of full-size
monoclonal antibodies over the last decades has motivated the pharmaceutical company to
develop various types of antibody formats in order to improve their efficacy and lower
adverse effects. By using strategies to miniaturize and multifunctionalize antibody molecules
new classes of antibody therapeutics, such as antibody derivatives (e.g., antibody–drug
conjugates and immunocytokines), bispecific/multispecific antibodies, antibody fragments,
were developed. In the future, with the progress of modern biotechnology, it can be expected
that these new-designed antibodies will finally pave the way for successful treatments of
various diseases., Otkriće monoklonskih antitela i njihova primena u terapiji je značajno uticala na
lečenje i zdravlje ljudi širom sveta. Danas, tri i po decenije nakon što je prvo monoklonsko
antitelo odobreno za upotrebu od strane Agencije za hranu i lekove Sjedinjenih Američkih
Država, više od 100 ovih terapeutika za lečenje malignih tumora i drugih bolesti se nalazi na
tržištu. Iako je ideja da se antitela mogu koristiti kao lekovi stara više od jednog veka, do
njene realizacije je došlo tek kada su naučnici uspostavili tehnologiju za dobijanje hibridoma
ćelija čime je bila omogućena proizvodnja antitela u laboratorijskim uslovima. S obzirom da
su ta prva terapijska antitela bila mišja i samim tim imunogena za čoveka, razvojem
tehnologije genetskog inženjeringa omogućeno je konstruisanje antitela koja su više
“humana” (tzv. himerna i humanizovana). Konačno, uspostavljanjem inovativnih platformi za
prikazivanje antitela ili njihovih fragmenata na fagima (“phage display”), generisanje miševa
koji sintetišu humana antitela ili izolaciju gena za antitela iz pojedinačne B ćelije omogućeno
je dobijanje potpuno humanih antitela. I pored više nego uspešne primene celih molekula
antitela u terapiji, da bi se prevazišla nedovoljna efikasnost nekih od njih i smanjili neželjeni
efekti, farmaceutske kompanije su počele da razvijaju različite formate antitela. Korišćenjem
strategije smanjenja veličine i/ili povećanja funkcionalnosti molekula antitela razvijena je
potpuno nova klasa terapijskih antitela kao što su derivati antitela (npr. konjugati antitela i
lekova), bispecifična/multispecifična antitela, fragmenti antitela i drugi. U budućnosti, sa
daljim razvojem moderne biotehnologije, može se očekivati da će ta novodizajnirana antitela
omogućiti uspešno lečenje mnogih bolesti.",
publisher = "Savez farmaceutskih udruženja Srbije (SFUS)",
journal = "Arhiv za farmaciju",
title = "Future perspectives of therapeutic monoclonal antibodies development: new formats and new functions, Dalji pravci razvoja terapijskih monoklonskih antitela: novi formati i nove funkcije",
volume = "72",
number = "4 suplement",
pages = "S35-S36",
url = "https://hdl.handle.net/21.15107/rcub_farfar_4441"
}
Stojić-Vukanić, Z.. (2022). Future perspectives of therapeutic monoclonal antibodies development: new formats and new functions. in Arhiv za farmaciju
Savez farmaceutskih udruženja Srbije (SFUS)., 72(4 suplement), S35-S36.
https://hdl.handle.net/21.15107/rcub_farfar_4441
Stojić-Vukanić Z. Future perspectives of therapeutic monoclonal antibodies development: new formats and new functions. in Arhiv za farmaciju. 2022;72(4 suplement):S35-S36.
https://hdl.handle.net/21.15107/rcub_farfar_4441 .
Stojić-Vukanić, Zorica, "Future perspectives of therapeutic monoclonal antibodies development: new formats and new functions" in Arhiv za farmaciju, 72, no. 4 suplement (2022):S35-S36,
https://hdl.handle.net/21.15107/rcub_farfar_4441 .

Biomarkers of aging-associated chronic inflammation as a prognostic factor for human longevity

Leposavić, Gordana; Stojić-Vukanić, Zorica

(Beograd : Savez farmaceutskih udruženja Srbije, 2022)

TY  - JOUR
AU  - Leposavić, Gordana
AU  - Stojić-Vukanić, Zorica
PY  - 2022
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/4184
AB  - It has been well-established that age-associated low-grade chronic inflammation
contributes to the development of a spectrum of chronic diseases, including diabetes mellitus,
ischemic heart disease, stroke, cancer, chronic kidney disease, non-alcoholic fatty liver disease
and neurodegenerative diseases, which affect the quality of life of the elderly and influence their
life span. This phenomenon is suggested to arise due to the weakening of the regulatory
mechanisms of the immune response, and the persistence of exogenous and endogenous
(reflecting oxidative cell injury) antigenic challenges, so it is referred to as oxi-inflamm-aging.
Considering that the development of age-associated chronic inflammation is “silent”, i.e., without
clinical signs until the aforementioned complications become apparent, it is important to identify
the biomarker(s) or pattern/cluster of biomarkers for this inflammation. It is also important to
define new strategies to combat the “silent” damage induced by chronic inflammation. Given that
at present there are no reliable biomarkers for chronic inflammation, this review points out the
problems in defining biomarker(s) or patterns/clusters of biomarkers for chronic inflammation in
order to stimulate further research and points to some possible routes of investigation.
AB  - Činjenično je dobro argumentovano da hronična inflamacija niskog stepena koja se javlja u toku starenja ima važnu ulogu u razvoju čitavog spektra hroničnih bolesti, uključujući šećernu bolest, ishemijsku bolest srca, moždani udar, malignu bolest, hronično oštećenje bubrega, nealkoholnu masnu bolest jetre, neurodegenerativne i autoimunske bolesti, koje utiču na kvalitet i dužinu života starih osoba. Smatra se da ovaj fenomen nastaje kao rezultat slabljenja regulatornih mehanizama imunskog sistema i perzistentnog izlaganja organizma delovanju egzogenih i endogenih (generisanih oštećenjem ćelija oksidativnim stresom) antigenskih izazova, što se u literaturi opisuje terminom oksidativno-inflamatorno starenje. Imajući u vidu da se hronična inflamacija razvija klinički "nemo", odnosno da postaje manifestna tek kada se razviju prethodno pomenute komplikacije, jasno je koliko je važno identifikovati biomarker(e) ili obrasce/klastere biomarkera te inflamacije. S obzirom na to da u ovom trenutku nema pouzdanih markera hronične inflamacije, ovaj pregledni rad je tako koncipiran da ukaže na probleme u identifikaciji biomarkera ili obrazaca/klastera biomarkera hronične inflamacije, s ciljem da stimuliše dalja istraživanja, ali i da da smernice za buduća istraživanja.
PB  - Beograd : Savez farmaceutskih udruženja Srbije
T2  - Arhiv za farmaciju
T1  - Biomarkers of aging-associated chronic inflammation as a prognostic factor for human longevity
T1  - Biomarkeri hronične inflamacije povezane sa starenjem kao prediktora dužine života
VL  - 72
IS  - 2
SP  - 91
EP  - 104
DO  - 10.5937/arhfarm72-36135
ER  - 
@article{
author = "Leposavić, Gordana and Stojić-Vukanić, Zorica",
year = "2022",
abstract = "It has been well-established that age-associated low-grade chronic inflammation
contributes to the development of a spectrum of chronic diseases, including diabetes mellitus,
ischemic heart disease, stroke, cancer, chronic kidney disease, non-alcoholic fatty liver disease
and neurodegenerative diseases, which affect the quality of life of the elderly and influence their
life span. This phenomenon is suggested to arise due to the weakening of the regulatory
mechanisms of the immune response, and the persistence of exogenous and endogenous
(reflecting oxidative cell injury) antigenic challenges, so it is referred to as oxi-inflamm-aging.
Considering that the development of age-associated chronic inflammation is “silent”, i.e., without
clinical signs until the aforementioned complications become apparent, it is important to identify
the biomarker(s) or pattern/cluster of biomarkers for this inflammation. It is also important to
define new strategies to combat the “silent” damage induced by chronic inflammation. Given that
at present there are no reliable biomarkers for chronic inflammation, this review points out the
problems in defining biomarker(s) or patterns/clusters of biomarkers for chronic inflammation in
order to stimulate further research and points to some possible routes of investigation., Činjenično je dobro argumentovano da hronična inflamacija niskog stepena koja se javlja u toku starenja ima važnu ulogu u razvoju čitavog spektra hroničnih bolesti, uključujući šećernu bolest, ishemijsku bolest srca, moždani udar, malignu bolest, hronično oštećenje bubrega, nealkoholnu masnu bolest jetre, neurodegenerativne i autoimunske bolesti, koje utiču na kvalitet i dužinu života starih osoba. Smatra se da ovaj fenomen nastaje kao rezultat slabljenja regulatornih mehanizama imunskog sistema i perzistentnog izlaganja organizma delovanju egzogenih i endogenih (generisanih oštećenjem ćelija oksidativnim stresom) antigenskih izazova, što se u literaturi opisuje terminom oksidativno-inflamatorno starenje. Imajući u vidu da se hronična inflamacija razvija klinički "nemo", odnosno da postaje manifestna tek kada se razviju prethodno pomenute komplikacije, jasno je koliko je važno identifikovati biomarker(e) ili obrasce/klastere biomarkera te inflamacije. S obzirom na to da u ovom trenutku nema pouzdanih markera hronične inflamacije, ovaj pregledni rad je tako koncipiran da ukaže na probleme u identifikaciji biomarkera ili obrazaca/klastera biomarkera hronične inflamacije, s ciljem da stimuliše dalja istraživanja, ali i da da smernice za buduća istraživanja.",
publisher = "Beograd : Savez farmaceutskih udruženja Srbije",
journal = "Arhiv za farmaciju",
title = "Biomarkers of aging-associated chronic inflammation as a prognostic factor for human longevity, Biomarkeri hronične inflamacije povezane sa starenjem kao prediktora dužine života",
volume = "72",
number = "2",
pages = "91-104",
doi = "10.5937/arhfarm72-36135"
}
Leposavić, G.,& Stojić-Vukanić, Z.. (2022). Biomarkers of aging-associated chronic inflammation as a prognostic factor for human longevity. in Arhiv za farmaciju
Beograd : Savez farmaceutskih udruženja Srbije., 72(2), 91-104.
https://doi.org/10.5937/arhfarm72-36135
Leposavić G, Stojić-Vukanić Z. Biomarkers of aging-associated chronic inflammation as a prognostic factor for human longevity. in Arhiv za farmaciju. 2022;72(2):91-104.
doi:10.5937/arhfarm72-36135 .
Leposavić, Gordana, Stojić-Vukanić, Zorica, "Biomarkers of aging-associated chronic inflammation as a prognostic factor for human longevity" in Arhiv za farmaciju, 72, no. 2 (2022):91-104,
https://doi.org/10.5937/arhfarm72-36135 . .

Sexual dimorphism in CX3CR1/Nrf2/HO‐1 spinal cord axis affects therapeutic efficacy of β‐adrenoceptor blockade in EAE rats

Pilipović, Ivan; Prijić, Ivana; Stojić-Vukanić, Zorica; Leposavić, Gordana

(2021)

TY  - CONF
AU  - Pilipović, Ivan
AU  - Prijić, Ivana
AU  - Stojić-Vukanić, Zorica
AU  - Leposavić, Gordana
PY  - 2021
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/4724
AB  - Our previous studies showed more severe EAE in male compared with female adult rats, and moderating effect of propranolol‐induced β‐adrenoceptor blockade on EAE in female rats through stimulation of Nrf2/HO‐1 signalling pathway in spinal cord microglia. This study was designed to examine putative sexual dimorphism in Nrf2/HO‐1 signalling pathway and CX3CL1, as one of its activators. Propranolol treatment beginning from the appearance of the first clinical signs of EAE mitigated the disease severity in rats of both sexes, but its effect was more prominent in males. This correlated with more prominent effect of propranolol on the expression of CX3CL1 in spinal cord tissue, CX3CR1 on microglial surface, and Nrf2/HO‐1 in spinal cord microglia in males. Consistently, the proportion of CX3CR1‐expressing microglia and CX3CR1 density on their surface increased more prominently in males. 
Consistently, propranolol increased the proportion of IL‐10/TGF‐β‐producing microglia and microglia expressing CD163, molecule highlighting ramified microglia with neuroprotective 
properties in damaged tissue, to a greater extent in males. Additionally, propranolol increased phagocyting capacity of microglia to a greater extent in males. Moreover, propranolol more prominently decreased the frequency of blood‐borne myeloid cells and highly pathogenic IL‐17+ T‐cells, coexpressing GM‐CSF/IFN‐γ, in male rat spinal cord. This correlated with greater reducing effect of propranolol on the spinal cord tissue expression of CCL2/CCL19/CCL21 chemokines in males. The study as a whole indicates that sexual dimorphism in CX3CR1/Nrf2/HO‐1 spinal cord axis could contribute to greater severity of EAE in male rats, and sexually dimorphic action of substances affecting its signalling capacity.
C3  - European Journal of Immunology
T1  - Sexual dimorphism in CX3CR1/Nrf2/HO‐1 spinal cord axis affects therapeutic efficacy of β‐adrenoceptor blockade in EAE rats
VL  - 51
IS  - Suppl.1
SP  - 246
EP  - 246
DO  - 10.1002/eji.202170200
ER  - 
@conference{
author = "Pilipović, Ivan and Prijić, Ivana and Stojić-Vukanić, Zorica and Leposavić, Gordana",
year = "2021",
abstract = "Our previous studies showed more severe EAE in male compared with female adult rats, and moderating effect of propranolol‐induced β‐adrenoceptor blockade on EAE in female rats through stimulation of Nrf2/HO‐1 signalling pathway in spinal cord microglia. This study was designed to examine putative sexual dimorphism in Nrf2/HO‐1 signalling pathway and CX3CL1, as one of its activators. Propranolol treatment beginning from the appearance of the first clinical signs of EAE mitigated the disease severity in rats of both sexes, but its effect was more prominent in males. This correlated with more prominent effect of propranolol on the expression of CX3CL1 in spinal cord tissue, CX3CR1 on microglial surface, and Nrf2/HO‐1 in spinal cord microglia in males. Consistently, the proportion of CX3CR1‐expressing microglia and CX3CR1 density on their surface increased more prominently in males. 
Consistently, propranolol increased the proportion of IL‐10/TGF‐β‐producing microglia and microglia expressing CD163, molecule highlighting ramified microglia with neuroprotective 
properties in damaged tissue, to a greater extent in males. Additionally, propranolol increased phagocyting capacity of microglia to a greater extent in males. Moreover, propranolol more prominently decreased the frequency of blood‐borne myeloid cells and highly pathogenic IL‐17+ T‐cells, coexpressing GM‐CSF/IFN‐γ, in male rat spinal cord. This correlated with greater reducing effect of propranolol on the spinal cord tissue expression of CCL2/CCL19/CCL21 chemokines in males. The study as a whole indicates that sexual dimorphism in CX3CR1/Nrf2/HO‐1 spinal cord axis could contribute to greater severity of EAE in male rats, and sexually dimorphic action of substances affecting its signalling capacity.",
journal = "European Journal of Immunology",
title = "Sexual dimorphism in CX3CR1/Nrf2/HO‐1 spinal cord axis affects therapeutic efficacy of β‐adrenoceptor blockade in EAE rats",
volume = "51",
number = "Suppl.1",
pages = "246-246",
doi = "10.1002/eji.202170200"
}
Pilipović, I., Prijić, I., Stojić-Vukanić, Z.,& Leposavić, G.. (2021). Sexual dimorphism in CX3CR1/Nrf2/HO‐1 spinal cord axis affects therapeutic efficacy of β‐adrenoceptor blockade in EAE rats. in European Journal of Immunology, 51(Suppl.1), 246-246.
https://doi.org/10.1002/eji.202170200
Pilipović I, Prijić I, Stojić-Vukanić Z, Leposavić G. Sexual dimorphism in CX3CR1/Nrf2/HO‐1 spinal cord axis affects therapeutic efficacy of β‐adrenoceptor blockade in EAE rats. in European Journal of Immunology. 2021;51(Suppl.1):246-246.
doi:10.1002/eji.202170200 .
Pilipović, Ivan, Prijić, Ivana, Stojić-Vukanić, Zorica, Leposavić, Gordana, "Sexual dimorphism in CX3CR1/Nrf2/HO‐1 spinal cord axis affects therapeutic efficacy of β‐adrenoceptor blockade in EAE rats" in European Journal of Immunology, 51, no. Suppl.1 (2021):246-246,
https://doi.org/10.1002/eji.202170200 . .
156
3

Блокада β-адренергичких рецептора појачава имунорегулаторна/имунопротективна својства микроглије: испитивање на моделу експерименталног аутоимунског енцефаломијелитиса

Prijić, Ivana; Pilipović, Ivan; Stojić-Vukanić, Zorica; Leposavić, Gordana

(Српска академија наука и уметности, 2021)

TY  - CONF
AU  - Prijić, Ivana
AU  - Pilipović, Ivan
AU  - Stojić-Vukanić, Zorica
AU  - Leposavić, Gordana
PY  - 2021
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/5089
AB  - Претпоставља се да дисфункција симпатичког нервног система 
доприноси развоју мултипле склерозе и експерименталног аутоимунског 
енцефаломијелитиса (ЕАЕ). Имајући у виду важност микроглије за 
развој/резолуцију неуроинфламације, испитиван је имуномодулаторни 
потенцијал главног симпатичког медијатора норадреналина коришћењем 
пацовског модела ЕАЕ-а. Резултати су показали да третман пропранололом, 
неселективним блокатором β-адренергичких рецептора, у ефекторској 
фази ЕАЕ-а смањује тежину болести. Ово је корелирало са повећаном 
заступљеношћу микроглије која експримира CX3CR1, кључан молекул за 
њену имуномодулаторну/неуропротективну активност, и њеном појачаном 
експресијом Nrf2 гена, као и гена за хем оксигеназу-1, која се сматра 
ефекторским молекулом анти-инфламаторног CX3CR1/Nrf2 сигналног 
пута. Истраживања in vitro показала су да активација β-адренергичких 
рецептора доводи до нисходне регулације експресије Nrf2 и путем 
независним од CX3CR1. Сходно претходним резултатима, пропранолол 
је повећао фагоцитну способност микроглије, што је корелирало са 
повећањем површинске експресије анти-инфламаторних маркера CD163 
и CD83. Повећање експресије хем оксигеназе-1 праћено је порастом 
заступљености микроглије која синтетише IL-10, а смањењем удела оне 
која експримира проинфламаторне цитокине IL-1β и IL-23. Пропранолол 
је смањио и експресију MCP-1/CCL2 у кичменој мождини. Консекутивно, 
инфилтрација кичмене мождине мијелоидним ћелијама и CD4+ Т-ћелијама 
била је смањена код пацова третираних пропранололом. У складу са свим 
претходним, пропранолол је лимитирао и реактивацију/пролиферацију 
CD4+ Т-лимфоцита и њихову диференцијацију у изузетно патогене IL 17+IFN-γ+GM-CSF+ ћелије. Студија указује да норадреналин, делујући 
посредством β-адренергичких рецептора, подстиче неуроинфламацију 
у ЕАЕ-у тако што модулише експресију Nrf2 у ћелијама микроглије. 
Такође, она представља могућу полазну основу за будућа транслациона 
фармаколошка истраживања у циљу дизајнирања нових приступа у лечењу 
мултипле склерозе.
PB  - Српска академија наука и уметности
PB  - Друштво имунолога Србије
C3  - Научни скуп - Светски дан имунологије 2021, 29. април 2021. године, Београд
T1  - Блокада β-адренергичких рецептора појачава имунорегулаторна/имунопротективна својства микроглије: испитивање на моделу експерименталног аутоимунског енцефаломијелитиса
UR  - https://hdl.handle.net/21.15107/rcub_farfar_5089
ER  - 
@conference{
author = "Prijić, Ivana and Pilipović, Ivan and Stojić-Vukanić, Zorica and Leposavić, Gordana",
year = "2021",
abstract = "Претпоставља се да дисфункција симпатичког нервног система 
доприноси развоју мултипле склерозе и експерименталног аутоимунског 
енцефаломијелитиса (ЕАЕ). Имајући у виду важност микроглије за 
развој/резолуцију неуроинфламације, испитиван је имуномодулаторни 
потенцијал главног симпатичког медијатора норадреналина коришћењем 
пацовског модела ЕАЕ-а. Резултати су показали да третман пропранололом, 
неселективним блокатором β-адренергичких рецептора, у ефекторској 
фази ЕАЕ-а смањује тежину болести. Ово је корелирало са повећаном 
заступљеношћу микроглије која експримира CX3CR1, кључан молекул за 
њену имуномодулаторну/неуропротективну активност, и њеном појачаном 
експресијом Nrf2 гена, као и гена за хем оксигеназу-1, која се сматра 
ефекторским молекулом анти-инфламаторног CX3CR1/Nrf2 сигналног 
пута. Истраживања in vitro показала су да активација β-адренергичких 
рецептора доводи до нисходне регулације експресије Nrf2 и путем 
независним од CX3CR1. Сходно претходним резултатима, пропранолол 
је повећао фагоцитну способност микроглије, што је корелирало са 
повећањем површинске експресије анти-инфламаторних маркера CD163 
и CD83. Повећање експресије хем оксигеназе-1 праћено је порастом 
заступљености микроглије која синтетише IL-10, а смањењем удела оне 
која експримира проинфламаторне цитокине IL-1β и IL-23. Пропранолол 
је смањио и експресију MCP-1/CCL2 у кичменој мождини. Консекутивно, 
инфилтрација кичмене мождине мијелоидним ћелијама и CD4+ Т-ћелијама 
била је смањена код пацова третираних пропранололом. У складу са свим 
претходним, пропранолол је лимитирао и реактивацију/пролиферацију 
CD4+ Т-лимфоцита и њихову диференцијацију у изузетно патогене IL 17+IFN-γ+GM-CSF+ ћелије. Студија указује да норадреналин, делујући 
посредством β-адренергичких рецептора, подстиче неуроинфламацију 
у ЕАЕ-у тако што модулише експресију Nrf2 у ћелијама микроглије. 
Такође, она представља могућу полазну основу за будућа транслациона 
фармаколошка истраживања у циљу дизајнирања нових приступа у лечењу 
мултипле склерозе.",
publisher = "Српска академија наука и уметности, Друштво имунолога Србије",
journal = "Научни скуп - Светски дан имунологије 2021, 29. април 2021. године, Београд",
title = "Блокада β-адренергичких рецептора појачава имунорегулаторна/имунопротективна својства микроглије: испитивање на моделу експерименталног аутоимунског енцефаломијелитиса",
url = "https://hdl.handle.net/21.15107/rcub_farfar_5089"
}
Prijić, I., Pilipović, I., Stojić-Vukanić, Z.,& Leposavić, G.. (2021). Блокада β-адренергичких рецептора појачава имунорегулаторна/имунопротективна својства микроглије: испитивање на моделу експерименталног аутоимунског енцефаломијелитиса. in Научни скуп - Светски дан имунологије 2021, 29. април 2021. године, Београд
Српска академија наука и уметности..
https://hdl.handle.net/21.15107/rcub_farfar_5089
Prijić I, Pilipović I, Stojić-Vukanić Z, Leposavić G. Блокада β-адренергичких рецептора појачава имунорегулаторна/имунопротективна својства микроглије: испитивање на моделу експерименталног аутоимунског енцефаломијелитиса. in Научни скуп - Светски дан имунологије 2021, 29. април 2021. године, Београд. 2021;.
https://hdl.handle.net/21.15107/rcub_farfar_5089 .
Prijić, Ivana, Pilipović, Ivan, Stojić-Vukanić, Zorica, Leposavić, Gordana, "Блокада β-адренергичких рецептора појачава имунорегулаторна/имунопротективна својства микроглије: испитивање на моделу експерименталног аутоимунског енцефаломијелитиса" in Научни скуп - Светски дан имунологије 2021, 29. април 2021. године, Београд (2021),
https://hdl.handle.net/21.15107/rcub_farfar_5089 .

Sex-specific remodeling of T-cell compartment with aging: Implications for rat susceptibility to central nervous system autoimmune diseases

Stojić-Vukanić, Zorica; Pilipović, Ivan; Arsenović-Ranin, Nevena; Dimitrijević, Mirjana; Leposavić, Gordana

(Elsevier B.V., 2021)

TY  - JOUR
AU  - Stojić-Vukanić, Zorica
AU  - Pilipović, Ivan
AU  - Arsenović-Ranin, Nevena
AU  - Dimitrijević, Mirjana
AU  - Leposavić, Gordana
PY  - 2021
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3946
AB  - The incidence of multiple sclerosis (MS) and susceptibility of animals to experimental autoimmune encephalomyelitis (EAE), the most commonly used experimental model of MS, decrease with aging. Generally, autoimmune diseases develop as the ultimate outcome of an imbalance between damaging immune responses against self and regulatory immune responses (keeping the former under control). Thus, in this review the age-related changes possibly underlying this balance were discussed. Specifically, considering the central role of T cells in MS/EAE, the impact of aging on overall functional capacity (reflecting both overall count and individual functional cell properties) of self-reactive conventional T cells (Tcons) and FoxP3+ regulatory T cells (Tregs), as the most potent immunoregulatory/suppressive cells, was analyzed, as well. The analysis encompasses three distinct compartments: thymus (the primary lymphoid organ responsible for the elimination of self-reactive T cells – negative selection and the generation of Tregs, compensating for imperfections of the negative selection), peripheral blood/lymphoid tissues (“afferent” compartment), and brain/spinal cord tissues (“target” compartment). Given that the incidence of MS and susceptibility of animals to EAE are greater in women/females than in age-matched men/males, sex as independent variable was also considered. In conclusion, with aging, sex-specific alterations in the balance of self-reactive Tcons/Tregs are likely to occur not only in the thymus/”afferent” compartment, but also in the “target” compartment, reflecting multifaceted changes in both T-cell types. Their in depth understanding is important not only for envisaging effects of aging, but also for designing interventions to slow-down aging without any adverse effect on incidence of autoimmune diseases.
PB  - Elsevier B.V.
T2  - Immunology Letters
T1  - Sex-specific remodeling of T-cell compartment with aging: Implications for rat susceptibility to central nervous system autoimmune diseases
VL  - 239
SP  - 42
EP  - 59
DO  - 10.1016/j.imlet.2021.08.003
ER  - 
@article{
author = "Stojić-Vukanić, Zorica and Pilipović, Ivan and Arsenović-Ranin, Nevena and Dimitrijević, Mirjana and Leposavić, Gordana",
year = "2021",
abstract = "The incidence of multiple sclerosis (MS) and susceptibility of animals to experimental autoimmune encephalomyelitis (EAE), the most commonly used experimental model of MS, decrease with aging. Generally, autoimmune diseases develop as the ultimate outcome of an imbalance between damaging immune responses against self and regulatory immune responses (keeping the former under control). Thus, in this review the age-related changes possibly underlying this balance were discussed. Specifically, considering the central role of T cells in MS/EAE, the impact of aging on overall functional capacity (reflecting both overall count and individual functional cell properties) of self-reactive conventional T cells (Tcons) and FoxP3+ regulatory T cells (Tregs), as the most potent immunoregulatory/suppressive cells, was analyzed, as well. The analysis encompasses three distinct compartments: thymus (the primary lymphoid organ responsible for the elimination of self-reactive T cells – negative selection and the generation of Tregs, compensating for imperfections of the negative selection), peripheral blood/lymphoid tissues (“afferent” compartment), and brain/spinal cord tissues (“target” compartment). Given that the incidence of MS and susceptibility of animals to EAE are greater in women/females than in age-matched men/males, sex as independent variable was also considered. In conclusion, with aging, sex-specific alterations in the balance of self-reactive Tcons/Tregs are likely to occur not only in the thymus/”afferent” compartment, but also in the “target” compartment, reflecting multifaceted changes in both T-cell types. Their in depth understanding is important not only for envisaging effects of aging, but also for designing interventions to slow-down aging without any adverse effect on incidence of autoimmune diseases.",
publisher = "Elsevier B.V.",
journal = "Immunology Letters",
title = "Sex-specific remodeling of T-cell compartment with aging: Implications for rat susceptibility to central nervous system autoimmune diseases",
volume = "239",
pages = "42-59",
doi = "10.1016/j.imlet.2021.08.003"
}
Stojić-Vukanić, Z., Pilipović, I., Arsenović-Ranin, N., Dimitrijević, M.,& Leposavić, G.. (2021). Sex-specific remodeling of T-cell compartment with aging: Implications for rat susceptibility to central nervous system autoimmune diseases. in Immunology Letters
Elsevier B.V.., 239, 42-59.
https://doi.org/10.1016/j.imlet.2021.08.003
Stojić-Vukanić Z, Pilipović I, Arsenović-Ranin N, Dimitrijević M, Leposavić G. Sex-specific remodeling of T-cell compartment with aging: Implications for rat susceptibility to central nervous system autoimmune diseases. in Immunology Letters. 2021;239:42-59.
doi:10.1016/j.imlet.2021.08.003 .
Stojić-Vukanić, Zorica, Pilipović, Ivan, Arsenović-Ranin, Nevena, Dimitrijević, Mirjana, Leposavić, Gordana, "Sex-specific remodeling of T-cell compartment with aging: Implications for rat susceptibility to central nervous system autoimmune diseases" in Immunology Letters, 239 (2021):42-59,
https://doi.org/10.1016/j.imlet.2021.08.003 . .
1

Inhibitors of tumor necrosis factor-α and mechanisms of their action

Bufan, Biljana; Jančić, Ivan; Stojić-Vukanić, Zorica

(Beograd : Savez farmaceutskih udruženja Srbije, 2020)

TY  - JOUR
AU  - Bufan, Biljana
AU  - Jančić, Ivan
AU  - Stojić-Vukanić, Zorica
PY  - 2020
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3642
AB  - Tumor necrosis factor (TNF)-α is a proinflammatory cytokine with a role in immunity to pathogens, as well as in the pathogenesis of several autoimmune/inflammatory diseases. Biological drugs targeting this cytokine and inhibiting its effects are designed. Until today, five TNF-α inhibitors are approved: infliximab, adalimumab, golimumab (monoclonal antibodies), certolizumab pegol (pegylated antigen-binding fragment of immunoglobulin), and etanercept [TNF receptor type 2-fragment crystallizable (Fc) of immunoglobulin fusion protein]. Their approved biosimilars are on the market, too. They are mainly used for the treatment of rheumatoid arthritis, inflammatory bowel disease, and psoriasis. Although TNF-α inhibitors are present in clinical practice for more than two decades and are established as an efficacious therapeutics, researchers are still occupied by revealing the complex mechanisms of their action. Namely, in addition to binding and neutralisation of soluble TNF-α, these drugs also bind/block transmembrane form of TNF-α (tmTNF-α), trigger diverse intracellular signals in tmTNF-α positive cells (a process named “reverse signalling”) or, if they have an Fc fragment, mediate killing of tmTNF-α-expressing cells by other immune cells or the complement system. Also, TNF-α inhibitors that contain Fc portion of the IgG antibody may affect Fc receptor-expressing cells and have an effector function quite independent of their TNF-α neutralisation capacity.
AB  - Faktor nekroze tumora (TNF)-a je citokin koji ima značajnu ulogu u patogenezi nekih autoimunskih/inflamatornih bolesti. Shodno tome, dizajnirani su biološki lekovi koji ciljano inhibiraju efekte koje on ostvaruje posredstvom svojih receptora. Do danas je odobreno pet lekova koji inhibiraju TNF-a: infliksimab, adalimumab, golimumab (monoklonska antitela), certolizumab pegol (pegilovani antigen-vezujući fragment imunoglobulina) i etanercept [TNF receptor 2-kristalizujući fragment (Fc) imunoglobulina fuzioni protein]. Takođe, brojni biosimilari ovih lekova su odobreni za primenu. Glavne indikacije za primenu anti-TNF-a lekova su: reumatoidni artritis, inflamatorne bolesti creva, psorijaza. Iako se TNF-a inhibitori više od dve decenije uspešno koriste u kliničkoj praksi, složeni mehanizmi njihovog delovanja još uvek nisu potpuno poznati. Naime, pokazano je da se ovi lekovi, osim vezivanja i neutralizacije solubilnog TNF-a, mogu vezati i za transmembransku formu ovog citokina i blokirati je i/ili pokrenuti prenos signala u ćeliju koja ispoljava ovaj molekul ("reverzni prenos signala"). Takođe, ovi lekovi, ukoliko poseduju Fc fragment, mogu posredovati i u ubijanju ćelija koje ispoljavaju membransku formu TNF-a aktivacijom drugih ćelija imunskog sistema ili sistema komplementa ili modulisati funkciju ćelija koje ispoljavaju receptore za Fc fragmanet i ostvarivati efektorske funkcije nezavisno od njihove sposobnosti da blokiraju/neutrališu TNF-a.
PB  - Beograd : Savez farmaceutskih udruženja Srbije
T2  - Arhiv za farmaciju
T1  - Inhibitors of tumor necrosis factor-α and mechanisms of their action
T1  - Inhibitori faktora nekroze tumora–α i mehanizmi njihovog dejstva
VL  - 70
IS  - 3
SP  - 109
EP  - 129
DO  - 10.5937/arhfarm2003109B
ER  - 
@article{
author = "Bufan, Biljana and Jančić, Ivan and Stojić-Vukanić, Zorica",
year = "2020",
abstract = "Tumor necrosis factor (TNF)-α is a proinflammatory cytokine with a role in immunity to pathogens, as well as in the pathogenesis of several autoimmune/inflammatory diseases. Biological drugs targeting this cytokine and inhibiting its effects are designed. Until today, five TNF-α inhibitors are approved: infliximab, adalimumab, golimumab (monoclonal antibodies), certolizumab pegol (pegylated antigen-binding fragment of immunoglobulin), and etanercept [TNF receptor type 2-fragment crystallizable (Fc) of immunoglobulin fusion protein]. Their approved biosimilars are on the market, too. They are mainly used for the treatment of rheumatoid arthritis, inflammatory bowel disease, and psoriasis. Although TNF-α inhibitors are present in clinical practice for more than two decades and are established as an efficacious therapeutics, researchers are still occupied by revealing the complex mechanisms of their action. Namely, in addition to binding and neutralisation of soluble TNF-α, these drugs also bind/block transmembrane form of TNF-α (tmTNF-α), trigger diverse intracellular signals in tmTNF-α positive cells (a process named “reverse signalling”) or, if they have an Fc fragment, mediate killing of tmTNF-α-expressing cells by other immune cells or the complement system. Also, TNF-α inhibitors that contain Fc portion of the IgG antibody may affect Fc receptor-expressing cells and have an effector function quite independent of their TNF-α neutralisation capacity., Faktor nekroze tumora (TNF)-a je citokin koji ima značajnu ulogu u patogenezi nekih autoimunskih/inflamatornih bolesti. Shodno tome, dizajnirani su biološki lekovi koji ciljano inhibiraju efekte koje on ostvaruje posredstvom svojih receptora. Do danas je odobreno pet lekova koji inhibiraju TNF-a: infliksimab, adalimumab, golimumab (monoklonska antitela), certolizumab pegol (pegilovani antigen-vezujući fragment imunoglobulina) i etanercept [TNF receptor 2-kristalizujući fragment (Fc) imunoglobulina fuzioni protein]. Takođe, brojni biosimilari ovih lekova su odobreni za primenu. Glavne indikacije za primenu anti-TNF-a lekova su: reumatoidni artritis, inflamatorne bolesti creva, psorijaza. Iako se TNF-a inhibitori više od dve decenije uspešno koriste u kliničkoj praksi, složeni mehanizmi njihovog delovanja još uvek nisu potpuno poznati. Naime, pokazano je da se ovi lekovi, osim vezivanja i neutralizacije solubilnog TNF-a, mogu vezati i za transmembransku formu ovog citokina i blokirati je i/ili pokrenuti prenos signala u ćeliju koja ispoljava ovaj molekul ("reverzni prenos signala"). Takođe, ovi lekovi, ukoliko poseduju Fc fragment, mogu posredovati i u ubijanju ćelija koje ispoljavaju membransku formu TNF-a aktivacijom drugih ćelija imunskog sistema ili sistema komplementa ili modulisati funkciju ćelija koje ispoljavaju receptore za Fc fragmanet i ostvarivati efektorske funkcije nezavisno od njihove sposobnosti da blokiraju/neutrališu TNF-a.",
publisher = "Beograd : Savez farmaceutskih udruženja Srbije",
journal = "Arhiv za farmaciju",
title = "Inhibitors of tumor necrosis factor-α and mechanisms of their action, Inhibitori faktora nekroze tumora–α i mehanizmi njihovog dejstva",
volume = "70",
number = "3",
pages = "109-129",
doi = "10.5937/arhfarm2003109B"
}
Bufan, B., Jančić, I.,& Stojić-Vukanić, Z.. (2020). Inhibitors of tumor necrosis factor-α and mechanisms of their action. in Arhiv za farmaciju
Beograd : Savez farmaceutskih udruženja Srbije., 70(3), 109-129.
https://doi.org/10.5937/arhfarm2003109B
Bufan B, Jančić I, Stojić-Vukanić Z. Inhibitors of tumor necrosis factor-α and mechanisms of their action. in Arhiv za farmaciju. 2020;70(3):109-129.
doi:10.5937/arhfarm2003109B .
Bufan, Biljana, Jančić, Ivan, Stojić-Vukanić, Zorica, "Inhibitors of tumor necrosis factor-α and mechanisms of their action" in Arhiv za farmaciju, 70, no. 3 (2020):109-129,
https://doi.org/10.5937/arhfarm2003109B . .

CD8+ T Cell-Mediated Mechanisms Contribute to the Progression of Neurocognitive Impairment in Both Multiple Sclerosis and Alzheimer's Disease?

Stojić-Vukanić, Zorica; Hadžibegović, Senka; Nicole, Olivier; Nacka-Aleksić, Mirjana; Leštarević, Sanja; Leposavić, Gordana

(Frontiers Media S.A., 2020)

TY  - JOUR
AU  - Stojić-Vukanić, Zorica
AU  - Hadžibegović, Senka
AU  - Nicole, Olivier
AU  - Nacka-Aleksić, Mirjana
AU  - Leštarević, Sanja
AU  - Leposavić, Gordana
PY  - 2020
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3750
AB  - Neurocognitive impairment (NCI) is one of the most relevant clinical manifestations of multiple sclerosis (MS). The profile of NCI and the structural and functional changes in the brain structures relevant for cognition in MS share some similarities to those in Alzheimer's disease (AD), the most common cause of neurocognitive disorders. Additionally, despite clear etiopathological differences between MS and AD, an accumulation of effector/memory CD8+ T cells and CD8+ tissue-resident memory T (Trm) cells in cognitively relevant brain structures of MS/AD patients, and higher frequency of effector/memory CD8+ T cells re-expressing CD45RA (TEMRA) with high capacity to secrete cytotoxic molecules and proinflammatory cytokines in their blood, were found. Thus, an active pathogenetic role of CD8+ T cells in the progression of MS and AD may be assumed. In this mini-review, findings supporting the putative role of CD8+ T cells in the pathogenesis of MS and AD are displayed, and putative mechanisms underlying their pathogenetic action are discussed. A special effort was made to identify the gaps in the current knowledge about the role of CD8+ T cells in the development of NCI to “catalyze” translational research leading to new feasible therapeutic interventions.
PB  - Frontiers Media S.A.
T2  - Frontiers in Immunology
T1  - CD8+ T Cell-Mediated Mechanisms Contribute to the Progression of Neurocognitive Impairment in Both Multiple Sclerosis and Alzheimer's Disease?
VL  - 11
DO  - 10.3389/fimmu.2020.566225
ER  - 
@article{
author = "Stojić-Vukanić, Zorica and Hadžibegović, Senka and Nicole, Olivier and Nacka-Aleksić, Mirjana and Leštarević, Sanja and Leposavić, Gordana",
year = "2020",
abstract = "Neurocognitive impairment (NCI) is one of the most relevant clinical manifestations of multiple sclerosis (MS). The profile of NCI and the structural and functional changes in the brain structures relevant for cognition in MS share some similarities to those in Alzheimer's disease (AD), the most common cause of neurocognitive disorders. Additionally, despite clear etiopathological differences between MS and AD, an accumulation of effector/memory CD8+ T cells and CD8+ tissue-resident memory T (Trm) cells in cognitively relevant brain structures of MS/AD patients, and higher frequency of effector/memory CD8+ T cells re-expressing CD45RA (TEMRA) with high capacity to secrete cytotoxic molecules and proinflammatory cytokines in their blood, were found. Thus, an active pathogenetic role of CD8+ T cells in the progression of MS and AD may be assumed. In this mini-review, findings supporting the putative role of CD8+ T cells in the pathogenesis of MS and AD are displayed, and putative mechanisms underlying their pathogenetic action are discussed. A special effort was made to identify the gaps in the current knowledge about the role of CD8+ T cells in the development of NCI to “catalyze” translational research leading to new feasible therapeutic interventions.",
publisher = "Frontiers Media S.A.",
journal = "Frontiers in Immunology",
title = "CD8+ T Cell-Mediated Mechanisms Contribute to the Progression of Neurocognitive Impairment in Both Multiple Sclerosis and Alzheimer's Disease?",
volume = "11",
doi = "10.3389/fimmu.2020.566225"
}
Stojić-Vukanić, Z., Hadžibegović, S., Nicole, O., Nacka-Aleksić, M., Leštarević, S.,& Leposavić, G.. (2020). CD8+ T Cell-Mediated Mechanisms Contribute to the Progression of Neurocognitive Impairment in Both Multiple Sclerosis and Alzheimer's Disease?. in Frontiers in Immunology
Frontiers Media S.A.., 11.
https://doi.org/10.3389/fimmu.2020.566225
Stojić-Vukanić Z, Hadžibegović S, Nicole O, Nacka-Aleksić M, Leštarević S, Leposavić G. CD8+ T Cell-Mediated Mechanisms Contribute to the Progression of Neurocognitive Impairment in Both Multiple Sclerosis and Alzheimer's Disease?. in Frontiers in Immunology. 2020;11.
doi:10.3389/fimmu.2020.566225 .
Stojić-Vukanić, Zorica, Hadžibegović, Senka, Nicole, Olivier, Nacka-Aleksić, Mirjana, Leštarević, Sanja, Leposavić, Gordana, "CD8+ T Cell-Mediated Mechanisms Contribute to the Progression of Neurocognitive Impairment in Both Multiple Sclerosis and Alzheimer's Disease?" in Frontiers in Immunology, 11 (2020),
https://doi.org/10.3389/fimmu.2020.566225 . .
10
26
2
25

Sex as a confounding factor in the effects of ageing on rat lymph node t cell compartment

Nacka-Aleksić, Mirjana; Stojić-Vukanić, Zorica; Pilipović, Ivan; Blagojević, Veljko; Kotur-Stevuljević, Jelena; Leposavić, Gordana

(Elsevier Inc., 2020)

TY  - JOUR
AU  - Nacka-Aleksić, Mirjana
AU  - Stojić-Vukanić, Zorica
AU  - Pilipović, Ivan
AU  - Blagojević, Veljko
AU  - Kotur-Stevuljević, Jelena
AU  - Leposavić, Gordana
PY  - 2020
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3734
AB  - The study examined the influence of sex on the alterations occurring with ageing in rat lymph node (LN) T cell compartment. In female and male rats the decrease in LN T cell counts was followed by a shift in CD4+/CD8+ T cell ratio towards CD8+ T cells, which was more prominent in males than in females. With ageing, in both major LN T cell subpopulations naïve (recent thymic emigrants and mature naïve cells) to memory/activated T cell ratio shifted to the side of memory/activated cells in female, and particularly in male rats. The frequency of regulatory CD25+Foxp3+ cells increased among LN CD4+/CD8+ T cells with ageing, reflecting, at least partly, an enhanced conversion of effector T cells into regulatory cells. This was also more prominent in male rats. The more prounounced increase in LN oxidative damage and the expression levels of proinflammatory cytokines in male rats with ageing, most likely contributed to the greater frequency of proinflammatory, replicatively senescent CD28- cells expressing CD11b (innate cell marker), among T cells of old male rats compared with age-matched females. The increase in LN oxidation/proinflammatory state with ageing was also consistent with the accumulation of exhausted PD-1high cells among T lymphocytes, particularly prominent among CD8+ T cells from male rats. Finally, by calculating a summary score for the key ageing-relevant parameters (an ageing index), a faster development of the deleterious changes in the T cell compartment occurring with ageing was confirmed in male rat LNs. Additionally, the study pointed to indices of LN T cell compartment ageing which correlate with those in peripheral blood.
PB  - Elsevier Inc.
T2  - Experimental Gerontology
T1  - Sex as a confounding factor in the effects of ageing on rat lymph node t cell compartment
VL  - 142
DO  - 10.1016/j.exger.2020.111140
ER  - 
@article{
author = "Nacka-Aleksić, Mirjana and Stojić-Vukanić, Zorica and Pilipović, Ivan and Blagojević, Veljko and Kotur-Stevuljević, Jelena and Leposavić, Gordana",
year = "2020",
abstract = "The study examined the influence of sex on the alterations occurring with ageing in rat lymph node (LN) T cell compartment. In female and male rats the decrease in LN T cell counts was followed by a shift in CD4+/CD8+ T cell ratio towards CD8+ T cells, which was more prominent in males than in females. With ageing, in both major LN T cell subpopulations naïve (recent thymic emigrants and mature naïve cells) to memory/activated T cell ratio shifted to the side of memory/activated cells in female, and particularly in male rats. The frequency of regulatory CD25+Foxp3+ cells increased among LN CD4+/CD8+ T cells with ageing, reflecting, at least partly, an enhanced conversion of effector T cells into regulatory cells. This was also more prominent in male rats. The more prounounced increase in LN oxidative damage and the expression levels of proinflammatory cytokines in male rats with ageing, most likely contributed to the greater frequency of proinflammatory, replicatively senescent CD28- cells expressing CD11b (innate cell marker), among T cells of old male rats compared with age-matched females. The increase in LN oxidation/proinflammatory state with ageing was also consistent with the accumulation of exhausted PD-1high cells among T lymphocytes, particularly prominent among CD8+ T cells from male rats. Finally, by calculating a summary score for the key ageing-relevant parameters (an ageing index), a faster development of the deleterious changes in the T cell compartment occurring with ageing was confirmed in male rat LNs. Additionally, the study pointed to indices of LN T cell compartment ageing which correlate with those in peripheral blood.",
publisher = "Elsevier Inc.",
journal = "Experimental Gerontology",
title = "Sex as a confounding factor in the effects of ageing on rat lymph node t cell compartment",
volume = "142",
doi = "10.1016/j.exger.2020.111140"
}
Nacka-Aleksić, M., Stojić-Vukanić, Z., Pilipović, I., Blagojević, V., Kotur-Stevuljević, J.,& Leposavić, G.. (2020). Sex as a confounding factor in the effects of ageing on rat lymph node t cell compartment. in Experimental Gerontology
Elsevier Inc.., 142.
https://doi.org/10.1016/j.exger.2020.111140
Nacka-Aleksić M, Stojić-Vukanić Z, Pilipović I, Blagojević V, Kotur-Stevuljević J, Leposavić G. Sex as a confounding factor in the effects of ageing on rat lymph node t cell compartment. in Experimental Gerontology. 2020;142.
doi:10.1016/j.exger.2020.111140 .
Nacka-Aleksić, Mirjana, Stojić-Vukanić, Zorica, Pilipović, Ivan, Blagojević, Veljko, Kotur-Stevuljević, Jelena, Leposavić, Gordana, "Sex as a confounding factor in the effects of ageing on rat lymph node t cell compartment" in Experimental Gerontology, 142 (2020),
https://doi.org/10.1016/j.exger.2020.111140 . .
2
2
2

Age and sex determine CD4+ T cell stimulatory and polarizing capacity of rat splenic dendritic cells

Stojić-Vukanić, Zorica; Pilipović, Ivan; Bufan, Biljana; Stojanović, Marija; Leposavić, Gordana

(Springer Nature, 2020)

TY  - JOUR
AU  - Stojić-Vukanić, Zorica
AU  - Pilipović, Ivan
AU  - Bufan, Biljana
AU  - Stojanović, Marija
AU  - Leposavić, Gordana
PY  - 2020
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3529
AB  - The study investigated influence of sex and age on splenic myeloid dendritic cells (DCs) from Dark Agouti rats. Freshly isolated DCs from young males exhibited less mature phenotype and greater endocytic capacity compared with those from age-matched females. Upon LPS stimulation in vitro they were less potent in stimulating allogeneic CD4+ cells in mixed leukocyte reaction (MLR), due to lower expression of MHC II, and greater NO and IL-10 production. In accordance with higher TGF-β production, young male rat DCs were less potent in stimulating IL-17 production in MLR than those from young females. Irrespective of sex, endocytic capacity and responsiveness of DCs to LPS stimulation in culture, judging by their allostimulatory capacity in MLR decreased with age, reflecting decline in MHC II surface density followed by their greater NO production; the effects more prominent in females. Additionally, compared with LPS-stimulated DCs from young rats, those from sex-matched aged rats were more potent in stimulating IL-10 production in MLR, whereas capacity of DCs from aged female and male rats to stimulate IL-17 production remained unaltered and decreased, respectively. This reflected age-related shift in IL-6/TGF-β production level ratio in LPS-stimulated DC cultures towards TGF-β, and sex-specific age-related remodeling CD4+ cell cytokine pathways. Additionally, compared with LPS-stimulated DCs from young rats, those cells from sex-matched aged rats were less potent in stimulating IFN-γ production in MLR, the effect particularly prominent in MLRs encompassing male rat DCs. The study showed that stimulatory and polarizing capacity of DCs depends on rat sex and age.
PB  - Springer Nature
T2  - Biogerontology
T1  - Age and sex determine CD4+ T cell stimulatory and polarizing capacity of rat splenic dendritic cells
VL  - 21
IS  - 1
SP  - 83
EP  - 107
DO  - 10.1007/s10522-019-09845-y
ER  - 
@article{
author = "Stojić-Vukanić, Zorica and Pilipović, Ivan and Bufan, Biljana and Stojanović, Marija and Leposavić, Gordana",
year = "2020",
abstract = "The study investigated influence of sex and age on splenic myeloid dendritic cells (DCs) from Dark Agouti rats. Freshly isolated DCs from young males exhibited less mature phenotype and greater endocytic capacity compared with those from age-matched females. Upon LPS stimulation in vitro they were less potent in stimulating allogeneic CD4+ cells in mixed leukocyte reaction (MLR), due to lower expression of MHC II, and greater NO and IL-10 production. In accordance with higher TGF-β production, young male rat DCs were less potent in stimulating IL-17 production in MLR than those from young females. Irrespective of sex, endocytic capacity and responsiveness of DCs to LPS stimulation in culture, judging by their allostimulatory capacity in MLR decreased with age, reflecting decline in MHC II surface density followed by their greater NO production; the effects more prominent in females. Additionally, compared with LPS-stimulated DCs from young rats, those from sex-matched aged rats were more potent in stimulating IL-10 production in MLR, whereas capacity of DCs from aged female and male rats to stimulate IL-17 production remained unaltered and decreased, respectively. This reflected age-related shift in IL-6/TGF-β production level ratio in LPS-stimulated DC cultures towards TGF-β, and sex-specific age-related remodeling CD4+ cell cytokine pathways. Additionally, compared with LPS-stimulated DCs from young rats, those cells from sex-matched aged rats were less potent in stimulating IFN-γ production in MLR, the effect particularly prominent in MLRs encompassing male rat DCs. The study showed that stimulatory and polarizing capacity of DCs depends on rat sex and age.",
publisher = "Springer Nature",
journal = "Biogerontology",
title = "Age and sex determine CD4+ T cell stimulatory and polarizing capacity of rat splenic dendritic cells",
volume = "21",
number = "1",
pages = "83-107",
doi = "10.1007/s10522-019-09845-y"
}
Stojić-Vukanić, Z., Pilipović, I., Bufan, B., Stojanović, M.,& Leposavić, G.. (2020). Age and sex determine CD4+ T cell stimulatory and polarizing capacity of rat splenic dendritic cells. in Biogerontology
Springer Nature., 21(1), 83-107.
https://doi.org/10.1007/s10522-019-09845-y
Stojić-Vukanić Z, Pilipović I, Bufan B, Stojanović M, Leposavić G. Age and sex determine CD4+ T cell stimulatory and polarizing capacity of rat splenic dendritic cells. in Biogerontology. 2020;21(1):83-107.
doi:10.1007/s10522-019-09845-y .
Stojić-Vukanić, Zorica, Pilipović, Ivan, Bufan, Biljana, Stojanović, Marija, Leposavić, Gordana, "Age and sex determine CD4+ T cell stimulatory and polarizing capacity of rat splenic dendritic cells" in Biogerontology, 21, no. 1 (2020):83-107,
https://doi.org/10.1007/s10522-019-09845-y . .
1
1
1

Propranolol diminished severity of rat EAE by enhancing immunoregulatory/protective properties of spinal cord microglia

Pilipović, Ivan; Stojić-Vukanić, Zorica; Prijić, Ivana; Jasnić, Nebojša; Leposavić, Gordana

(Elsevier, 2020)

TY  - JOUR
AU  - Pilipović, Ivan
AU  - Stojić-Vukanić, Zorica
AU  - Prijić, Ivana
AU  - Jasnić, Nebojša
AU  - Leposavić, Gordana
PY  - 2020
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3509
AB  - Sympathetic dysfunction is suggested to contribute to development of multiple sclerosis and experimental autoimmune encephalomyelitis (EAE) alike. Considering important role of microglia in development/resolution of neuroinflammation, contribution of noradrenaline, the key sympathetic end-point mediator, in modulation of microglial phenotypic and functional properties in rat EAE model was examined. The study showed that noradrenaline acting in neurocrine and autocrine/paracrine way might influence microglia during EAE. Propranolol treatment over the effector phase moderated EAE course. This was associated with the increased proportion of microglia expressing CX3CR1, the key molecule in their immunomodulatory/neuroprotective action, and upregulation of CX3CR1 downstream Nrf2 gene. This correlated with the increased heme oxygenase-1 (HO-1) expression and phagocytic capacity of microglia, and their phenotypic changes mirrored in increased proportion of CD163- and CD83-expressing cells. The enhanced HO-1 expression was linked with the decreased proportion of microglial cells expressing IL-1β and IL-23, and possibly IL-6, followed by increased proportion of IL- 10–expressing microglia, and downregulated MCP-1/CCL2 expression. Consistently, spinal cord infiltration with blood-borne myeloid and CD4+ T cells, as well as CD4+ T-cell reactivation/proliferation and differentiation into highly pathogenic IL-17+ cells co-producing IFN-γ and GM-CSF were decreased in propranolol-treated rats compared with saline-injected controls. The in vitro investigations of the effects of noradrenaline on microglia showed that noradrenaline through β-adrenoceptor may influence Nrf2 expression also via CX3CR1-independent route. The study suggests β-adrenoceptor–mediated neuroinflammation-promoting role of noradrenaline in EAE via modulation of microglial Nrf2 expression, and thereby forms the basis for further translational pharmacological research to improve multiple sclerosis therapy.
PB  - Elsevier
T2  - Neurobiology of Disease
T1  - Propranolol diminished severity of rat EAE by enhancing immunoregulatory/protective properties of spinal cord microglia
VL  - 134
DO  - 10.1016/j.nbd.2019.104665
ER  - 
@article{
author = "Pilipović, Ivan and Stojić-Vukanić, Zorica and Prijić, Ivana and Jasnić, Nebojša and Leposavić, Gordana",
year = "2020",
abstract = "Sympathetic dysfunction is suggested to contribute to development of multiple sclerosis and experimental autoimmune encephalomyelitis (EAE) alike. Considering important role of microglia in development/resolution of neuroinflammation, contribution of noradrenaline, the key sympathetic end-point mediator, in modulation of microglial phenotypic and functional properties in rat EAE model was examined. The study showed that noradrenaline acting in neurocrine and autocrine/paracrine way might influence microglia during EAE. Propranolol treatment over the effector phase moderated EAE course. This was associated with the increased proportion of microglia expressing CX3CR1, the key molecule in their immunomodulatory/neuroprotective action, and upregulation of CX3CR1 downstream Nrf2 gene. This correlated with the increased heme oxygenase-1 (HO-1) expression and phagocytic capacity of microglia, and their phenotypic changes mirrored in increased proportion of CD163- and CD83-expressing cells. The enhanced HO-1 expression was linked with the decreased proportion of microglial cells expressing IL-1β and IL-23, and possibly IL-6, followed by increased proportion of IL- 10–expressing microglia, and downregulated MCP-1/CCL2 expression. Consistently, spinal cord infiltration with blood-borne myeloid and CD4+ T cells, as well as CD4+ T-cell reactivation/proliferation and differentiation into highly pathogenic IL-17+ cells co-producing IFN-γ and GM-CSF were decreased in propranolol-treated rats compared with saline-injected controls. The in vitro investigations of the effects of noradrenaline on microglia showed that noradrenaline through β-adrenoceptor may influence Nrf2 expression also via CX3CR1-independent route. The study suggests β-adrenoceptor–mediated neuroinflammation-promoting role of noradrenaline in EAE via modulation of microglial Nrf2 expression, and thereby forms the basis for further translational pharmacological research to improve multiple sclerosis therapy.",
publisher = "Elsevier",
journal = "Neurobiology of Disease",
title = "Propranolol diminished severity of rat EAE by enhancing immunoregulatory/protective properties of spinal cord microglia",
volume = "134",
doi = "10.1016/j.nbd.2019.104665"
}
Pilipović, I., Stojić-Vukanić, Z., Prijić, I., Jasnić, N.,& Leposavić, G.. (2020). Propranolol diminished severity of rat EAE by enhancing immunoregulatory/protective properties of spinal cord microglia. in Neurobiology of Disease
Elsevier., 134.
https://doi.org/10.1016/j.nbd.2019.104665
Pilipović I, Stojić-Vukanić Z, Prijić I, Jasnić N, Leposavić G. Propranolol diminished severity of rat EAE by enhancing immunoregulatory/protective properties of spinal cord microglia. in Neurobiology of Disease. 2020;134.
doi:10.1016/j.nbd.2019.104665 .
Pilipović, Ivan, Stojić-Vukanić, Zorica, Prijić, Ivana, Jasnić, Nebojša, Leposavić, Gordana, "Propranolol diminished severity of rat EAE by enhancing immunoregulatory/protective properties of spinal cord microglia" in Neurobiology of Disease, 134 (2020),
https://doi.org/10.1016/j.nbd.2019.104665 . .
15
7
16

Role of the End-Point Mediators of Sympathoadrenal and Sympathoneural Stress Axes in the Pathogenesis of Experimental Autoimmune Encephalomyelitis and Multiple Sclerosis

Pilipović, Iivan; Stojić-Vukanić, Zorica; Prijić, Ivana; Leposavić, Gordana

(Frontiers Media S.A., 2020)

TY  - JOUR
AU  - Pilipović, Iivan
AU  - Stojić-Vukanić, Zorica
AU  - Prijić, Ivana
AU  - Leposavić, Gordana
PY  - 2020
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3503
AB  - The role of stress effector systems in the initiation and progression of multiple sclerosis (MS) and experimental autoimmune encephalomyelitis (EAE), the most commonly used experimental model of MS, has strongly been suggested. To corroborate this notion, alterations in activity of the sympathoadrenal and sympathoneural axes of sympathoadrenal system (a major communication pathway between the central nervous system and the immune system), mirrored in altered release of their end-point mediators (adrenaline and noradrenaline, respectively), are shown to precede (in MS) and/or occur during development of MS and EAE in response to immune cell activation (in early phase of disease) and disease-related damage of sympathoadrenal system neurons and their projections (in late phase of disease). To add to the complexity, innate immunity cells and T-lymphocytes synthesize noradrenaline that may be implicated in a local autocrine/paracrine self-amplifying feed-forward loop to enhance myeloid-cell synthesis of proinflammatory cytokines and inflammatory injury. Furthermore, experimental manipulations targeting noradrenaline/adrenaline action are shown to influence clinical outcome of EAE, in a disease phase-specific manner. This is partly related to the fact that virtually all types of cells involved in the instigation and progression of autoimmune inflammation and target tissue damage in EAE/MS express functional adrenoceptors. Although catecholamines exert majority of immunomodulatory effects through β2-adrenoceptor, a role for α-adrenoceptors in EAE pathogenesis has also been indicated. In this review, we summarize all aforementioned aspects of immunopathogenetic action of catecholamines in EAE/MS as possibly important for designing new strategies targeting their action to prevent/mitigate autoimmune neuroinflammation and tissue damage.
PB  - Frontiers Media S.A.
T2  - Frontiers in Endocrinology
T1  - Role of the End-Point Mediators of Sympathoadrenal and Sympathoneural Stress Axes in the Pathogenesis of Experimental Autoimmune Encephalomyelitis and Multiple Sclerosis
VL  - 10
DO  - 10.3389/fendo.2019.00921
ER  - 
@article{
author = "Pilipović, Iivan and Stojić-Vukanić, Zorica and Prijić, Ivana and Leposavić, Gordana",
year = "2020",
abstract = "The role of stress effector systems in the initiation and progression of multiple sclerosis (MS) and experimental autoimmune encephalomyelitis (EAE), the most commonly used experimental model of MS, has strongly been suggested. To corroborate this notion, alterations in activity of the sympathoadrenal and sympathoneural axes of sympathoadrenal system (a major communication pathway between the central nervous system and the immune system), mirrored in altered release of their end-point mediators (adrenaline and noradrenaline, respectively), are shown to precede (in MS) and/or occur during development of MS and EAE in response to immune cell activation (in early phase of disease) and disease-related damage of sympathoadrenal system neurons and their projections (in late phase of disease). To add to the complexity, innate immunity cells and T-lymphocytes synthesize noradrenaline that may be implicated in a local autocrine/paracrine self-amplifying feed-forward loop to enhance myeloid-cell synthesis of proinflammatory cytokines and inflammatory injury. Furthermore, experimental manipulations targeting noradrenaline/adrenaline action are shown to influence clinical outcome of EAE, in a disease phase-specific manner. This is partly related to the fact that virtually all types of cells involved in the instigation and progression of autoimmune inflammation and target tissue damage in EAE/MS express functional adrenoceptors. Although catecholamines exert majority of immunomodulatory effects through β2-adrenoceptor, a role for α-adrenoceptors in EAE pathogenesis has also been indicated. In this review, we summarize all aforementioned aspects of immunopathogenetic action of catecholamines in EAE/MS as possibly important for designing new strategies targeting their action to prevent/mitigate autoimmune neuroinflammation and tissue damage.",
publisher = "Frontiers Media S.A.",
journal = "Frontiers in Endocrinology",
title = "Role of the End-Point Mediators of Sympathoadrenal and Sympathoneural Stress Axes in the Pathogenesis of Experimental Autoimmune Encephalomyelitis and Multiple Sclerosis",
volume = "10",
doi = "10.3389/fendo.2019.00921"
}
Pilipović, I., Stojić-Vukanić, Z., Prijić, I.,& Leposavić, G.. (2020). Role of the End-Point Mediators of Sympathoadrenal and Sympathoneural Stress Axes in the Pathogenesis of Experimental Autoimmune Encephalomyelitis and Multiple Sclerosis. in Frontiers in Endocrinology
Frontiers Media S.A.., 10.
https://doi.org/10.3389/fendo.2019.00921
Pilipović I, Stojić-Vukanić Z, Prijić I, Leposavić G. Role of the End-Point Mediators of Sympathoadrenal and Sympathoneural Stress Axes in the Pathogenesis of Experimental Autoimmune Encephalomyelitis and Multiple Sclerosis. in Frontiers in Endocrinology. 2020;10.
doi:10.3389/fendo.2019.00921 .
Pilipović, Iivan, Stojić-Vukanić, Zorica, Prijić, Ivana, Leposavić, Gordana, "Role of the End-Point Mediators of Sympathoadrenal and Sympathoneural Stress Axes in the Pathogenesis of Experimental Autoimmune Encephalomyelitis and Multiple Sclerosis" in Frontiers in Endocrinology, 10 (2020),
https://doi.org/10.3389/fendo.2019.00921 . .
2
4
1
3

Natural killer cells as participants in pathogenesis of rat experimental autoimmune encephalomyelitis (EAE): Lessons from research on rats with distinct age and strain

Đuretić, Jasmina; Pilipović, Ivan; Stojić-Vukanić, Zorica; Leposavić, Gordana

(Termedia Publishing House Ltd., 2019)

TY  - JOUR
AU  - Đuretić, Jasmina
AU  - Pilipović, Ivan
AU  - Stojić-Vukanić, Zorica
AU  - Leposavić, Gordana
PY  - 2019
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3571
AB  - Natural killer (NK) cells, influencing dendritic cell (DC)-mediated CD4+ lymphocyte priming in draining lymph nodes (dLNs) and controlling spinal cord (SC) infiltration with encephalitogenic CD4+T lymphocytes, modulate EAE (multiple sclerosis model). This study examined their putative contribution to age-related differences in EAE development in Dark Agouti (DA) (exhibiting age-related decrease in EAE susceptibility) and Albino Oxford (AO) (becoming susceptible to EAE with aging) rats. Aging increased NK cell number in dLNs from rats of both strains. In AO rats, but not in DA ones, it also increased the numbers of IFN-γ-producing NK cells (important for DC activation) and activated/matured DCs, thereby increasing activated/matured DC/conventional Foxp3-CD4+ cell ratio and activated CD25+Foxp3-CD4+ cell number. Aging in DA rats diminished activated/matured DC/conventional Foxp3-CD4+ cell ratio and activated Foxp3-CD4+ cell number. However, MBP-stimulated CD4+ cell proliferation did not differ in dLN cell cultures from young and aged AO rats (as more favorable activated/matured DC/Foxp3-CD4+ cell ratio was abrogated by lower intrinsic CD4+ cell proliferative capacity and a greater regulatory CD25+Foxp3+CD4+ lymphocyte frequency), but was lower in those from aged compared with young DA rats. At SC level, aging shifted Foxp3-CD4+/cytotoxic CX3CR1+ NK cell ratio towards the former in AO rats, so it was less favorable in aged AO rats exhibiting prolonged neurological deficit compared with their DA counterparts. The study showed strain and age differences in number of IFN-γ-producing NK cells in EAE rat dLNs, and suggested that their pathogenetic relevance depends on frequency and/or activity of other cells involved in CD4+ T cell (auto)immune response.
PB  - Termedia Publishing House Ltd.
T2  - Central European Journal of Immunology
T1  - Natural killer cells as participants in pathogenesis of rat experimental autoimmune encephalomyelitis (EAE): Lessons from research on rats with distinct age and strain
VL  - 44
IS  - 4
SP  - 337
EP  - 356
DO  - 10.5114/ceji.2019.92777
ER  - 
@article{
author = "Đuretić, Jasmina and Pilipović, Ivan and Stojić-Vukanić, Zorica and Leposavić, Gordana",
year = "2019",
abstract = "Natural killer (NK) cells, influencing dendritic cell (DC)-mediated CD4+ lymphocyte priming in draining lymph nodes (dLNs) and controlling spinal cord (SC) infiltration with encephalitogenic CD4+T lymphocytes, modulate EAE (multiple sclerosis model). This study examined their putative contribution to age-related differences in EAE development in Dark Agouti (DA) (exhibiting age-related decrease in EAE susceptibility) and Albino Oxford (AO) (becoming susceptible to EAE with aging) rats. Aging increased NK cell number in dLNs from rats of both strains. In AO rats, but not in DA ones, it also increased the numbers of IFN-γ-producing NK cells (important for DC activation) and activated/matured DCs, thereby increasing activated/matured DC/conventional Foxp3-CD4+ cell ratio and activated CD25+Foxp3-CD4+ cell number. Aging in DA rats diminished activated/matured DC/conventional Foxp3-CD4+ cell ratio and activated Foxp3-CD4+ cell number. However, MBP-stimulated CD4+ cell proliferation did not differ in dLN cell cultures from young and aged AO rats (as more favorable activated/matured DC/Foxp3-CD4+ cell ratio was abrogated by lower intrinsic CD4+ cell proliferative capacity and a greater regulatory CD25+Foxp3+CD4+ lymphocyte frequency), but was lower in those from aged compared with young DA rats. At SC level, aging shifted Foxp3-CD4+/cytotoxic CX3CR1+ NK cell ratio towards the former in AO rats, so it was less favorable in aged AO rats exhibiting prolonged neurological deficit compared with their DA counterparts. The study showed strain and age differences in number of IFN-γ-producing NK cells in EAE rat dLNs, and suggested that their pathogenetic relevance depends on frequency and/or activity of other cells involved in CD4+ T cell (auto)immune response.",
publisher = "Termedia Publishing House Ltd.",
journal = "Central European Journal of Immunology",
title = "Natural killer cells as participants in pathogenesis of rat experimental autoimmune encephalomyelitis (EAE): Lessons from research on rats with distinct age and strain",
volume = "44",
number = "4",
pages = "337-356",
doi = "10.5114/ceji.2019.92777"
}
Đuretić, J., Pilipović, I., Stojić-Vukanić, Z.,& Leposavić, G.. (2019). Natural killer cells as participants in pathogenesis of rat experimental autoimmune encephalomyelitis (EAE): Lessons from research on rats with distinct age and strain. in Central European Journal of Immunology
Termedia Publishing House Ltd.., 44(4), 337-356.
https://doi.org/10.5114/ceji.2019.92777
Đuretić J, Pilipović I, Stojić-Vukanić Z, Leposavić G. Natural killer cells as participants in pathogenesis of rat experimental autoimmune encephalomyelitis (EAE): Lessons from research on rats with distinct age and strain. in Central European Journal of Immunology. 2019;44(4):337-356.
doi:10.5114/ceji.2019.92777 .
Đuretić, Jasmina, Pilipović, Ivan, Stojić-Vukanić, Zorica, Leposavić, Gordana, "Natural killer cells as participants in pathogenesis of rat experimental autoimmune encephalomyelitis (EAE): Lessons from research on rats with distinct age and strain" in Central European Journal of Immunology, 44, no. 4 (2019):337-356,
https://doi.org/10.5114/ceji.2019.92777 . .
3
2
3

Propranolol reduced severity of EAE by increasing the expression Nrf2 in microglia

Pilipović, Ivan; Prijić, Ivana; Stojić-Vukanić, Zorica; Leposavić, Gordana

(Institute for Biological Research "Siniša Stanković" National Institute of Republic of Serbia, 2019)

TY  - CONF
AU  - Pilipović, Ivan
AU  - Prijić, Ivana
AU  - Stojić-Vukanić, Zorica
AU  - Leposavić, Gordana
PY  - 2019
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/5085
AB  - Sympathetic dysfunction was proposed to participate in development of multiple sclerosis and 
its animal model, experimental autoimmune encephalomyelitis (EAE). This may be linked with 
findings indicating that noradrenaline, the key sympathetic end-point mediator, through β adrenoceptor exerts immunomodulatory action. Considering importance of the target tissue for 
the clinical outcome of EAE, the study investigated the effects of propranolol, a non-selective β adrenoceptor blocker, on the disease severity in Dark Agouti rats. Administration of propranolol 
over the effector phase of EAE substantially moderated neurological symptoms of the disease. 
This correlated with the increased proportion of spinal cord microglia expressing CX3CR1, the 
crucial neuroinflammation-limiting molecule, and upregulated expression of Nrf2, the key 
CX3CR1 downstream target gene. Additionally, in spinal cord of propranolol-administered rats 
the expression of heme-oxigenase 1, Nrf2 target gene, was upregulated. Consequently, microglia 
from propranolol-administered rats, exhibited increased proportion of IL-10–expressing cells, 
but decreased those of IL-1β– and IL-23–expressing ones. Propranolol also downregulated the 
IL-6 and MCP-1/CCL2 expression in spinal cord. Furthermore, propranolol affecting 
CXCR1/Nrf2 signaling pathway enhanced microglial phagocytic/endocytic capacity and surface 
expression of anti-inflammatory CD163/CD83 markers. Results from in vitro pharmacological 
study examining influence of noradrenaline/propranolol on functional properties of microglia 
showed that microglia synthesize noradrenaline, which, in turn, through β-adrenoceptor, 
downregulated their Nrf2 expression, in a CX3CR1-independent manner. In accordance with 
microglial shift towards a more anti-inflammatory profile, in spinal cord of propranolol administered rats was found: i) decreased infiltration with blood-borne myeloid and CD4+ T 
cells, and ii) reduced CD4+ T-cell reactivation/proliferation and differentiation into highly 
pathogenic IL-17+ cells co-producing IFN-γ and GM-CSF. The study suggests a 
neuroinflammation-promoting role for central noradrenaline in EAE, via β-adrenoceptor–
mediated modulation of microglial Nrf2 expression. Thus, it points out to a putative target for 
future translational pharmacological research to optimize multiple sclerosis therapy. Funding: 
MPNTR RS (grant number 175050)
PB  - Institute for Biological Research "Siniša Stanković" National Institute of Republic of Serbia
PB  - Immunological Society of Serbia
C3  - Immunology at the confluence of multidisciplinary approaces, Belgrade December 6.-8.  2019, Abstract book
T1  - Propranolol reduced severity of EAE by increasing the expression Nrf2 in microglia
UR  - https://hdl.handle.net/21.15107/rcub_farfar_5085
ER  - 
@conference{
author = "Pilipović, Ivan and Prijić, Ivana and Stojić-Vukanić, Zorica and Leposavić, Gordana",
year = "2019",
abstract = "Sympathetic dysfunction was proposed to participate in development of multiple sclerosis and 
its animal model, experimental autoimmune encephalomyelitis (EAE). This may be linked with 
findings indicating that noradrenaline, the key sympathetic end-point mediator, through β adrenoceptor exerts immunomodulatory action. Considering importance of the target tissue for 
the clinical outcome of EAE, the study investigated the effects of propranolol, a non-selective β adrenoceptor blocker, on the disease severity in Dark Agouti rats. Administration of propranolol 
over the effector phase of EAE substantially moderated neurological symptoms of the disease. 
This correlated with the increased proportion of spinal cord microglia expressing CX3CR1, the 
crucial neuroinflammation-limiting molecule, and upregulated expression of Nrf2, the key 
CX3CR1 downstream target gene. Additionally, in spinal cord of propranolol-administered rats 
the expression of heme-oxigenase 1, Nrf2 target gene, was upregulated. Consequently, microglia 
from propranolol-administered rats, exhibited increased proportion of IL-10–expressing cells, 
but decreased those of IL-1β– and IL-23–expressing ones. Propranolol also downregulated the 
IL-6 and MCP-1/CCL2 expression in spinal cord. Furthermore, propranolol affecting 
CXCR1/Nrf2 signaling pathway enhanced microglial phagocytic/endocytic capacity and surface 
expression of anti-inflammatory CD163/CD83 markers. Results from in vitro pharmacological 
study examining influence of noradrenaline/propranolol on functional properties of microglia 
showed that microglia synthesize noradrenaline, which, in turn, through β-adrenoceptor, 
downregulated their Nrf2 expression, in a CX3CR1-independent manner. In accordance with 
microglial shift towards a more anti-inflammatory profile, in spinal cord of propranolol administered rats was found: i) decreased infiltration with blood-borne myeloid and CD4+ T 
cells, and ii) reduced CD4+ T-cell reactivation/proliferation and differentiation into highly 
pathogenic IL-17+ cells co-producing IFN-γ and GM-CSF. The study suggests a 
neuroinflammation-promoting role for central noradrenaline in EAE, via β-adrenoceptor–
mediated modulation of microglial Nrf2 expression. Thus, it points out to a putative target for 
future translational pharmacological research to optimize multiple sclerosis therapy. Funding: 
MPNTR RS (grant number 175050)",
publisher = "Institute for Biological Research "Siniša Stanković" National Institute of Republic of Serbia, Immunological Society of Serbia",
journal = "Immunology at the confluence of multidisciplinary approaces, Belgrade December 6.-8.  2019, Abstract book",
title = "Propranolol reduced severity of EAE by increasing the expression Nrf2 in microglia",
url = "https://hdl.handle.net/21.15107/rcub_farfar_5085"
}
Pilipović, I., Prijić, I., Stojić-Vukanić, Z.,& Leposavić, G.. (2019). Propranolol reduced severity of EAE by increasing the expression Nrf2 in microglia. in Immunology at the confluence of multidisciplinary approaces, Belgrade December 6.-8.  2019, Abstract book
Institute for Biological Research "Siniša Stanković" National Institute of Republic of Serbia..
https://hdl.handle.net/21.15107/rcub_farfar_5085
Pilipović I, Prijić I, Stojić-Vukanić Z, Leposavić G. Propranolol reduced severity of EAE by increasing the expression Nrf2 in microglia. in Immunology at the confluence of multidisciplinary approaces, Belgrade December 6.-8.  2019, Abstract book. 2019;.
https://hdl.handle.net/21.15107/rcub_farfar_5085 .
Pilipović, Ivan, Prijić, Ivana, Stojić-Vukanić, Zorica, Leposavić, Gordana, "Propranolol reduced severity of EAE by increasing the expression Nrf2 in microglia" in Immunology at the confluence of multidisciplinary approaces, Belgrade December 6.-8.  2019, Abstract book (2019),
https://hdl.handle.net/21.15107/rcub_farfar_5085 .

Adjuvants in vaccines registered for human use

Filipić, Brankica; Stojić-Vukanić, Zorica

(Beograd : Savez farmaceutskih udruženja Srbije, 2019)

TY  - JOUR
AU  - Filipić, Brankica
AU  - Stojić-Vukanić, Zorica
PY  - 2019
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3565
AB  - Vaccination is one of the most efficient strategies for prevention of infection diseases, but with introduction of sub-unit vaccines with lower immunogenicity adjuvants were needed to enhance the immune response. The term adjuvant is from Latin verb adjuvare which means „to aid”. Adjuvants have been used in vaccines for more than 90 years. The longest adjuvant history belongs to aluminium salts, but novel adjuvants have been introduced in licensed vaccines in last 30 years. These novel adjuvants are AS04, which consists of aluminium hydroxide and Toll-like receptor 4 (TLR4) agonist monophosphoryl lipid A and is used in hepatitis B vaccine Fendrix® and HPV vaccine Cervarix®, emulsion based adjuvants which are part of several influenza vaccines-MF59 (Fluad® and Focetria®) and AS03 (Pandemrix®), AS01 liposomal adjuvant which is combination of two distinct immunostimulatory molecules and is component of herpes zoster and malaria vaccine and virosomes included in hepatits A vaccine (Epaxal®) and influenza vaccines (Inflexal® V and Invivac®). Adjuvant development and better insight into their mechanism of action are of great importance in order to replace empirical with rational use of adjuvants, without affecting vaccine safety.
AB  - Vakcinacija je jedna od najznačajnijih strategija za prevenciju infektivnih oboljenja, a razvoj subjediničnih vakcina doveo je do potrebe za primenom adjuvanasa u vakcinama. Naziv adjuvans potiče od latinske reči adjuvare što znači "pomoći". Adjuvansi su supstance koje se primenjuju u vakcinama više od 90 godina, a dodaju se da bi se povećala imunogenost antigena koji imaju nizak imunostimulatorni potencijal. U vakcinama za primenu kod ljudi, najduže se kao adjuvansi koriste soli aluminijuma, ali je poslednjih decenija nekoliko novih adjuvanasa uključeno u vakcine koje su odobrene za primenu. Adjuvantni sistem AS04, ulazi u sastav vakcina protiv humanog papiloma virusa (Cervarix®) i hepatitis B virusa (Fendrix®) i sadrži aluminijum hidroksid i TLR4 agonist, monofosforil lipid A. Zatim, adjuvansi na bazi emulzije (MF59 i AS03) su sastavni deo vakcina protiv gripa (Fluad®, Focetria® i Pandemrix®). Kombinacija dva imunostimulatorna molekula, označena kao AS01, ulazi u sastav vakcine protiv herpes zoster virusa i malarije dok se adjuvansi na bazi virozoma koriste u vakcinama protiv hepatitisa A (Epaxal®) i gripa (Inflexal® V, Invivac®). Daljim razvojem adjuvanasa, i ispitivanjem njihovog mehanizma delovanja oni će se umesto empirijski, sve više koristili racionalno i ciljano, čime će se postići bolji imunogeni profil vakcina, bez narušavanja njihovog bezbednosnog profila.
PB  - Beograd : Savez farmaceutskih udruženja Srbije
T2  - Arhiv za farmaciju
T1  - Adjuvants in vaccines registered for human use
T1  - Adjuvansi u vakcinama registrovanim    za primenu kod ljudi
VL  - 69
IS  - 6
SP  - 406
EP  - 419
DO  - 10.5937/arhfarm1906406F
ER  - 
@article{
author = "Filipić, Brankica and Stojić-Vukanić, Zorica",
year = "2019",
abstract = "Vaccination is one of the most efficient strategies for prevention of infection diseases, but with introduction of sub-unit vaccines with lower immunogenicity adjuvants were needed to enhance the immune response. The term adjuvant is from Latin verb adjuvare which means „to aid”. Adjuvants have been used in vaccines for more than 90 years. The longest adjuvant history belongs to aluminium salts, but novel adjuvants have been introduced in licensed vaccines in last 30 years. These novel adjuvants are AS04, which consists of aluminium hydroxide and Toll-like receptor 4 (TLR4) agonist monophosphoryl lipid A and is used in hepatitis B vaccine Fendrix® and HPV vaccine Cervarix®, emulsion based adjuvants which are part of several influenza vaccines-MF59 (Fluad® and Focetria®) and AS03 (Pandemrix®), AS01 liposomal adjuvant which is combination of two distinct immunostimulatory molecules and is component of herpes zoster and malaria vaccine and virosomes included in hepatits A vaccine (Epaxal®) and influenza vaccines (Inflexal® V and Invivac®). Adjuvant development and better insight into their mechanism of action are of great importance in order to replace empirical with rational use of adjuvants, without affecting vaccine safety., Vakcinacija je jedna od najznačajnijih strategija za prevenciju infektivnih oboljenja, a razvoj subjediničnih vakcina doveo je do potrebe za primenom adjuvanasa u vakcinama. Naziv adjuvans potiče od latinske reči adjuvare što znači "pomoći". Adjuvansi su supstance koje se primenjuju u vakcinama više od 90 godina, a dodaju se da bi se povećala imunogenost antigena koji imaju nizak imunostimulatorni potencijal. U vakcinama za primenu kod ljudi, najduže se kao adjuvansi koriste soli aluminijuma, ali je poslednjih decenija nekoliko novih adjuvanasa uključeno u vakcine koje su odobrene za primenu. Adjuvantni sistem AS04, ulazi u sastav vakcina protiv humanog papiloma virusa (Cervarix®) i hepatitis B virusa (Fendrix®) i sadrži aluminijum hidroksid i TLR4 agonist, monofosforil lipid A. Zatim, adjuvansi na bazi emulzije (MF59 i AS03) su sastavni deo vakcina protiv gripa (Fluad®, Focetria® i Pandemrix®). Kombinacija dva imunostimulatorna molekula, označena kao AS01, ulazi u sastav vakcine protiv herpes zoster virusa i malarije dok se adjuvansi na bazi virozoma koriste u vakcinama protiv hepatitisa A (Epaxal®) i gripa (Inflexal® V, Invivac®). Daljim razvojem adjuvanasa, i ispitivanjem njihovog mehanizma delovanja oni će se umesto empirijski, sve više koristili racionalno i ciljano, čime će se postići bolji imunogeni profil vakcina, bez narušavanja njihovog bezbednosnog profila.",
publisher = "Beograd : Savez farmaceutskih udruženja Srbije",
journal = "Arhiv za farmaciju",
title = "Adjuvants in vaccines registered for human use, Adjuvansi u vakcinama registrovanim    za primenu kod ljudi",
volume = "69",
number = "6",
pages = "406-419",
doi = "10.5937/arhfarm1906406F"
}
Filipić, B.,& Stojić-Vukanić, Z.. (2019). Adjuvants in vaccines registered for human use. in Arhiv za farmaciju
Beograd : Savez farmaceutskih udruženja Srbije., 69(6), 406-419.
https://doi.org/10.5937/arhfarm1906406F
Filipić B, Stojić-Vukanić Z. Adjuvants in vaccines registered for human use. in Arhiv za farmaciju. 2019;69(6):406-419.
doi:10.5937/arhfarm1906406F .
Filipić, Brankica, Stojić-Vukanić, Zorica, "Adjuvants in vaccines registered for human use" in Arhiv za farmaciju, 69, no. 6 (2019):406-419,
https://doi.org/10.5937/arhfarm1906406F . .

Active immunotherapy of cancer: An overview of therapeutic vaccines

Filipić, Brankica; Stojić-Vukanić, Zorica

(Beograd : Savez farmaceutskih udruženja Srbije, 2019)

TY  - JOUR
AU  - Filipić, Brankica
AU  - Stojić-Vukanić, Zorica
PY  - 2019
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3563
AB  - Cancer is one of the leading causes of morbidity and mortality worldwide and great efforts are underway to develop new therapeutic protocols. One of the approaches is immunotherapy which uses the immune system and its components to fight against cancer. The two main axes of cancer immunotherapy refer to passive and active treatments. Passive immunotherapy includes administration of tumor-specific antibodies and autologous T cells which destroy tumor cells, while active immunotherapy is directed at inducing the patient´s own antitumor immune responses and refers to cancer vaccines and immune checkpoint inhibitors. Vaccination of tumor-bearing individuals with tumor cells/antigens or autologous dendritic cells pulsed with tumor antigens may result in enhanced antitumor immune response. However, vaccine design is a complex, multi-component task, and the optimal combinations of antigens, adjuvants, delivery methods and routes of administration need to be precisely defined. Active immunotherapy also addresses the immunosuppressive and tolerogenic mechanisms developed by tumors. This review provides an overview of new results from clinical studies of therapeutic cancer vaccines and discusses their implications for the clinical use, alone or in combination with other immunotherapeutic strategies.
AB  - Maligni tumor (rak, karcinom) je jedan od vodećih uzroka obolevanja i smrtnosti pa se veliki  napori  ulažu  u  razvoj  novih  terapijskih  pristupa.  Savremena  imunoterapija  malignih tumora  obuhvata  primenu  antitumorskih  antitela  i  autologih  T  ćelija  koje  uništavaju  ćelije tumora (pasivna imunoterapija) i pojačanje slabog antitumorskog imunskog odgovora domaćina (aktivna imunoterapija) vakcinacijom i primenom antitela koja blokiraju inhibitorne receptore (kontrolne tačke) T limfocita. Vakcinacija pacijenata obolelih od tumora njihovim sopstvenim tumorskim  ćelijama,  antigenima  tih  ćelija  ili  dendritskim  ćelijama  koje  su  inkubirane  sa tumorskim  antigenima  stimuliše  imunski  sistem  pacijenta  da  prepozna  tumorske  antigene  i eliminiše maligne ćelije. Međutim, razvoj terapijskih tumorskih vakcina suočen je sa brojnim izazovima  vezanim  za  njihov  dizajn,  u  smislu  optimalne  kombinacije  antigena,  adjuvansa  i nosača, kao i za način primene. Pored toga, savremena aktivna imunoterapija treba da prevaziđe nisku imunogenost tumora i imunosupresivne mehanizme mikrosredine tumora kod pacijenata sa klinički ispoljenom bolesti. U ovom radu prikazani su rezultati novijih kliničkih studija u kojima  su  ispitivane  različite  terapijske  vakcine  za  karcinom  i  diskutovano  je  o  njihovoj mogućoj  primeni  u  kliničkoj  praksi,  kako  samih,  tako  i  u  kombinaciji  sa  drugim imunoterapijama.
PB  - Beograd : Savez farmaceutskih udruženja Srbije
T2  - Arhiv za farmaciju
T1  - Active immunotherapy of cancer: An overview of therapeutic vaccines
T1  - Aktivna imunoterapija malignih tumora: pregled terapijskih vakcina
VL  - 69
IS  - 6
SP  - 490
EP  - 506
DO  - 10.5937/arhfarm1906490F
ER  - 
@article{
author = "Filipić, Brankica and Stojić-Vukanić, Zorica",
year = "2019",
abstract = "Cancer is one of the leading causes of morbidity and mortality worldwide and great efforts are underway to develop new therapeutic protocols. One of the approaches is immunotherapy which uses the immune system and its components to fight against cancer. The two main axes of cancer immunotherapy refer to passive and active treatments. Passive immunotherapy includes administration of tumor-specific antibodies and autologous T cells which destroy tumor cells, while active immunotherapy is directed at inducing the patient´s own antitumor immune responses and refers to cancer vaccines and immune checkpoint inhibitors. Vaccination of tumor-bearing individuals with tumor cells/antigens or autologous dendritic cells pulsed with tumor antigens may result in enhanced antitumor immune response. However, vaccine design is a complex, multi-component task, and the optimal combinations of antigens, adjuvants, delivery methods and routes of administration need to be precisely defined. Active immunotherapy also addresses the immunosuppressive and tolerogenic mechanisms developed by tumors. This review provides an overview of new results from clinical studies of therapeutic cancer vaccines and discusses their implications for the clinical use, alone or in combination with other immunotherapeutic strategies., Maligni tumor (rak, karcinom) je jedan od vodećih uzroka obolevanja i smrtnosti pa se veliki  napori  ulažu  u  razvoj  novih  terapijskih  pristupa.  Savremena  imunoterapija  malignih tumora  obuhvata  primenu  antitumorskih  antitela  i  autologih  T  ćelija  koje  uništavaju  ćelije tumora (pasivna imunoterapija) i pojačanje slabog antitumorskog imunskog odgovora domaćina (aktivna imunoterapija) vakcinacijom i primenom antitela koja blokiraju inhibitorne receptore (kontrolne tačke) T limfocita. Vakcinacija pacijenata obolelih od tumora njihovim sopstvenim tumorskim  ćelijama,  antigenima  tih  ćelija  ili  dendritskim  ćelijama  koje  su  inkubirane  sa tumorskim  antigenima  stimuliše  imunski  sistem  pacijenta  da  prepozna  tumorske  antigene  i eliminiše maligne ćelije. Međutim, razvoj terapijskih tumorskih vakcina suočen je sa brojnim izazovima  vezanim  za  njihov  dizajn,  u  smislu  optimalne  kombinacije  antigena,  adjuvansa  i nosača, kao i za način primene. Pored toga, savremena aktivna imunoterapija treba da prevaziđe nisku imunogenost tumora i imunosupresivne mehanizme mikrosredine tumora kod pacijenata sa klinički ispoljenom bolesti. U ovom radu prikazani su rezultati novijih kliničkih studija u kojima  su  ispitivane  različite  terapijske  vakcine  za  karcinom  i  diskutovano  je  o  njihovoj mogućoj  primeni  u  kliničkoj  praksi,  kako  samih,  tako  i  u  kombinaciji  sa  drugim imunoterapijama.",
publisher = "Beograd : Savez farmaceutskih udruženja Srbije",
journal = "Arhiv za farmaciju",
title = "Active immunotherapy of cancer: An overview of therapeutic vaccines, Aktivna imunoterapija malignih tumora: pregled terapijskih vakcina",
volume = "69",
number = "6",
pages = "490-506",
doi = "10.5937/arhfarm1906490F"
}
Filipić, B.,& Stojić-Vukanić, Z.. (2019). Active immunotherapy of cancer: An overview of therapeutic vaccines. in Arhiv za farmaciju
Beograd : Savez farmaceutskih udruženja Srbije., 69(6), 490-506.
https://doi.org/10.5937/arhfarm1906490F
Filipić B, Stojić-Vukanić Z. Active immunotherapy of cancer: An overview of therapeutic vaccines. in Arhiv za farmaciju. 2019;69(6):490-506.
doi:10.5937/arhfarm1906490F .
Filipić, Brankica, Stojić-Vukanić, Zorica, "Active immunotherapy of cancer: An overview of therapeutic vaccines" in Arhiv za farmaciju, 69, no. 6 (2019):490-506,
https://doi.org/10.5937/arhfarm1906490F . .

Noradrenaline through beta-adrenoceptor contributes to sexual dimorphism in primary CD4+T-cell response in DA rat EAE model?

Vujnović, Ivana; Pilipović, Ivan; Jasnić, Nebojša; Petrović, Raisa; Blagojević, Veljko; Arsenović-Ranin, Nevena; Stojić-Vukanić, Zorica; Đorđević, Jelena; Leposavić, Gordana

(Academic Press Inc Elsevier Science, San Diego, 2019)

TY  - JOUR
AU  - Vujnović, Ivana
AU  - Pilipović, Ivan
AU  - Jasnić, Nebojša
AU  - Petrović, Raisa
AU  - Blagojević, Veljko
AU  - Arsenović-Ranin, Nevena
AU  - Stojić-Vukanić, Zorica
AU  - Đorđević, Jelena
AU  - Leposavić, Gordana
PY  - 2019
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3323
AB  - Males exhibit stronger sympathetic nervous system (SNS) activity, but weaker primary CD4 + T-cell (auto) immune responses. To test the role of catecholamines, major end-point SNS mediators, in this dimorphism, influence of propranolol (beta-adrenoceptor blocker) on mitogen/neuroantigen-stimulated CD4 + T cells from female and male EAE rat draining lymph node (dLN) cell cultures was examined. Male rat dLNs exhibited higher noradrenaline concentration and frequency of beta(2)-adrenoceptor-expressing CD4 + T lymphocytes and antigen presenting cells. Propranolol, irrespective of exogenous noradrenaline presence, more prominently augmented IL-2 production and proliferation of CD4 + lymphocytes in male than female rat dLN cell cultures. In neuroantigen-stimulated dLN cells of both sexes propranolol increased IL-1 beta and IL-23/p19 expression and IL-17 + CD4 + cell frequency, but enhanced IL-17 production only in male rat CD4 + lymphocytes, thereby abrogating sexual dimorphism in IL-17 concentration observed in propranolol-free cultures. Thus, beta-adrenoceptor-mediated signalling may contribute to sex bias in rat IL-17-producing cell secretory capacity.
PB  - Academic Press Inc Elsevier Science, San Diego
T2  - Cellular Immunology
T1  - Noradrenaline through beta-adrenoceptor contributes to sexual dimorphism in primary CD4+T-cell response in DA rat EAE model?
VL  - 336
SP  - 48
EP  - 57
DO  - 10.1016/j.cellimm.2018.12.009
ER  - 
@article{
author = "Vujnović, Ivana and Pilipović, Ivan and Jasnić, Nebojša and Petrović, Raisa and Blagojević, Veljko and Arsenović-Ranin, Nevena and Stojić-Vukanić, Zorica and Đorđević, Jelena and Leposavić, Gordana",
year = "2019",
abstract = "Males exhibit stronger sympathetic nervous system (SNS) activity, but weaker primary CD4 + T-cell (auto) immune responses. To test the role of catecholamines, major end-point SNS mediators, in this dimorphism, influence of propranolol (beta-adrenoceptor blocker) on mitogen/neuroantigen-stimulated CD4 + T cells from female and male EAE rat draining lymph node (dLN) cell cultures was examined. Male rat dLNs exhibited higher noradrenaline concentration and frequency of beta(2)-adrenoceptor-expressing CD4 + T lymphocytes and antigen presenting cells. Propranolol, irrespective of exogenous noradrenaline presence, more prominently augmented IL-2 production and proliferation of CD4 + lymphocytes in male than female rat dLN cell cultures. In neuroantigen-stimulated dLN cells of both sexes propranolol increased IL-1 beta and IL-23/p19 expression and IL-17 + CD4 + cell frequency, but enhanced IL-17 production only in male rat CD4 + lymphocytes, thereby abrogating sexual dimorphism in IL-17 concentration observed in propranolol-free cultures. Thus, beta-adrenoceptor-mediated signalling may contribute to sex bias in rat IL-17-producing cell secretory capacity.",
publisher = "Academic Press Inc Elsevier Science, San Diego",
journal = "Cellular Immunology",
title = "Noradrenaline through beta-adrenoceptor contributes to sexual dimorphism in primary CD4+T-cell response in DA rat EAE model?",
volume = "336",
pages = "48-57",
doi = "10.1016/j.cellimm.2018.12.009"
}
Vujnović, I., Pilipović, I., Jasnić, N., Petrović, R., Blagojević, V., Arsenović-Ranin, N., Stojić-Vukanić, Z., Đorđević, J.,& Leposavić, G.. (2019). Noradrenaline through beta-adrenoceptor contributes to sexual dimorphism in primary CD4+T-cell response in DA rat EAE model?. in Cellular Immunology
Academic Press Inc Elsevier Science, San Diego., 336, 48-57.
https://doi.org/10.1016/j.cellimm.2018.12.009
Vujnović I, Pilipović I, Jasnić N, Petrović R, Blagojević V, Arsenović-Ranin N, Stojić-Vukanić Z, Đorđević J, Leposavić G. Noradrenaline through beta-adrenoceptor contributes to sexual dimorphism in primary CD4+T-cell response in DA rat EAE model?. in Cellular Immunology. 2019;336:48-57.
doi:10.1016/j.cellimm.2018.12.009 .
Vujnović, Ivana, Pilipović, Ivan, Jasnić, Nebojša, Petrović, Raisa, Blagojević, Veljko, Arsenović-Ranin, Nevena, Stojić-Vukanić, Zorica, Đorđević, Jelena, Leposavić, Gordana, "Noradrenaline through beta-adrenoceptor contributes to sexual dimorphism in primary CD4+T-cell response in DA rat EAE model?" in Cellular Immunology, 336 (2019):48-57,
https://doi.org/10.1016/j.cellimm.2018.12.009 . .
1
14
9
13

Propranolol Impairs Primary Immune Responses in Rat Experimental Autoimmune Encephalomyelitis

Pilipović, Ivan; Vujnović, Ivana; Petrović, Raisa; Stojić-Vukanić, Zorica; Leposavić, Gordana

(S. Karger AG, 2019)

TY  - JOUR
AU  - Pilipović, Ivan
AU  - Vujnović, Ivana
AU  - Petrović, Raisa
AU  - Stojić-Vukanić, Zorica
AU  - Leposavić, Gordana
PY  - 2019
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3263
AB  - Objective: We examined the effect of β-adrenoceptor (AR) blockade in the preclinical phase of experimental autoimmune encephalomyelitis (EAE), the most commonly used model of multiple sclerosis, on the development of primary CD4+ T-cell responses in draining lymph nodes (dLNs). Methods: CD11b+ cell migration to dLNs, CD4+ T-cell activation/proliferation, and IL-17+ CD4+ (Th17) cell numbers in dLN and spinal cord (SC) were examined in male and female Dark Agouti rats using flow cytometry analysis. Results: Irrespective of sex, in propranolol-treated (PT) rats, migration of CD11b+ antigen-presenting cells from the site of immunization to dLNs was impaired compared with saline-treated controls and consequently the frequency of all CD11b+ cells in dLNs and activated cells among them, too. This correlated with decreased expression of CCL19/21 transcripts in dLNs. Consistently, the frequency of activated/proliferating cells among dLN CD4+ T cells was reduced in PT rats. Additionally, propranolol reduced the number of Th17 cells in dLNs and SC. Consistently, male and female PT rats exhibited a decreased incidence of EAE and prolonged duration of the asymptomatic disease phase. Conclusion: This study suggests that sympathetic dysregulation is involved in the outbreak of clinical EAE.
PB  - S. Karger AG
T2  - NeuroImmunoModulation
T1  - Propranolol Impairs Primary Immune Responses in Rat Experimental Autoimmune Encephalomyelitis
DO  - 10.1159/000500094
ER  - 
@article{
author = "Pilipović, Ivan and Vujnović, Ivana and Petrović, Raisa and Stojić-Vukanić, Zorica and Leposavić, Gordana",
year = "2019",
abstract = "Objective: We examined the effect of β-adrenoceptor (AR) blockade in the preclinical phase of experimental autoimmune encephalomyelitis (EAE), the most commonly used model of multiple sclerosis, on the development of primary CD4+ T-cell responses in draining lymph nodes (dLNs). Methods: CD11b+ cell migration to dLNs, CD4+ T-cell activation/proliferation, and IL-17+ CD4+ (Th17) cell numbers in dLN and spinal cord (SC) were examined in male and female Dark Agouti rats using flow cytometry analysis. Results: Irrespective of sex, in propranolol-treated (PT) rats, migration of CD11b+ antigen-presenting cells from the site of immunization to dLNs was impaired compared with saline-treated controls and consequently the frequency of all CD11b+ cells in dLNs and activated cells among them, too. This correlated with decreased expression of CCL19/21 transcripts in dLNs. Consistently, the frequency of activated/proliferating cells among dLN CD4+ T cells was reduced in PT rats. Additionally, propranolol reduced the number of Th17 cells in dLNs and SC. Consistently, male and female PT rats exhibited a decreased incidence of EAE and prolonged duration of the asymptomatic disease phase. Conclusion: This study suggests that sympathetic dysregulation is involved in the outbreak of clinical EAE.",
publisher = "S. Karger AG",
journal = "NeuroImmunoModulation",
title = "Propranolol Impairs Primary Immune Responses in Rat Experimental Autoimmune Encephalomyelitis",
doi = "10.1159/000500094"
}
Pilipović, I., Vujnović, I., Petrović, R., Stojić-Vukanić, Z.,& Leposavić, G.. (2019). Propranolol Impairs Primary Immune Responses in Rat Experimental Autoimmune Encephalomyelitis. in NeuroImmunoModulation
S. Karger AG..
https://doi.org/10.1159/000500094
Pilipović I, Vujnović I, Petrović R, Stojić-Vukanić Z, Leposavić G. Propranolol Impairs Primary Immune Responses in Rat Experimental Autoimmune Encephalomyelitis. in NeuroImmunoModulation. 2019;.
doi:10.1159/000500094 .
Pilipović, Ivan, Vujnović, Ivana, Petrović, Raisa, Stojić-Vukanić, Zorica, Leposavić, Gordana, "Propranolol Impairs Primary Immune Responses in Rat Experimental Autoimmune Encephalomyelitis" in NeuroImmunoModulation (2019),
https://doi.org/10.1159/000500094 . .
6
3
6

Strain differences in thymic atrophy in rats immunized for EAE correlate with the clinical outcome of immunization

Nacka-Aleksić, Mirjana; Stojanović, Marija; Pilipović, Ivan; Stojić-Vukanić, Zorica; Kosec, Duško; Leposavić, Gordana

(Public Library Science, San Francisco, 2018)

TY  - JOUR
AU  - Nacka-Aleksić, Mirjana
AU  - Stojanović, Marija
AU  - Pilipović, Ivan
AU  - Stojić-Vukanić, Zorica
AU  - Kosec, Duško
AU  - Leposavić, Gordana
PY  - 2018
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3221
AB  - An accumulating body of evidence suggests that development of autoimmune pathologies leads to thymic dysfunction and changes in peripheral T-cell compartment, which, in turn, perpetuate their pathogenesis. To test this hypothesis, thymocyte differentiation/maturation in rats susceptible (Dark Agouti, DA) and relatively resistant (Albino Oxford, AO) to experimental autoimmune encephalomyelitis (EAE) induction was examined. Irrespective of strain, immunization for EAE (i) increased the circulating levels of IL-6, a cytokine causally linked with thymic atrophy, and (ii) led to thymic atrophy reflecting partly enhanced thymocyte apoptosis associated with downregulated thymic IL-7 expression. Additionally, immunization diminished the expression of Thy-1, a negative regulator of TCR alpha beta-mediated signaling and activation thresholds, on CD4+CD8+ TCR alpha beta(lo/hi) thymocytes undergoing selection and thereby impaired thymocyte selection/survival. This diminished the generation of mature CD4+ and CD8+ single positive TCR alpha beta(hi) thymocytes and, consequently, CD4+ and CD8+ recent thymic emigrants. In immunized rats, thymic differentiation of natural regulatory CD4+Foxp3+CD25+ T cells (nTregs) was particularly affected reflecting a diminished expression of IL-7, IL-2 and IL-15. The decline in the overall thymic T-cell output and nTreg generation was more pronounced in DA than AO rats. Additionally, differently from immunized AO rats, in DA ones the frequency of CD28- cells secreting cytolytic enzymes within peripheral blood CD4+ T lymphocytes increased, as a consequence of thymic atrophy-related replicative stress (mirrored in CD4+ cell memory pool expansion and p16(INK4a) accumulation). The higher circulating level of TNF-alpha in DA compared with AO rats could also contribute to this difference. Consistently, higher frequency of cytolytic CD4+ granzyme B+ cells (associated with greater tissue damage) was found in spinal cord of immunized DA rats compared with their AO counterparts. In conclusion, the study indicated that strain differences in immunization-induced changes in thymopoiesis and peripheral CD4+CD28- T-cell generation could contribute to rat strain-specific clinical outcomes of immunization for EAE.
PB  - Public Library Science, San Francisco
T2  - PLoS One
T1  - Strain differences in thymic atrophy in rats immunized for EAE correlate with the clinical outcome of immunization
VL  - 13
IS  - 8
DO  - 10.1371/journal.pone.0201848
ER  - 
@article{
author = "Nacka-Aleksić, Mirjana and Stojanović, Marija and Pilipović, Ivan and Stojić-Vukanić, Zorica and Kosec, Duško and Leposavić, Gordana",
year = "2018",
abstract = "An accumulating body of evidence suggests that development of autoimmune pathologies leads to thymic dysfunction and changes in peripheral T-cell compartment, which, in turn, perpetuate their pathogenesis. To test this hypothesis, thymocyte differentiation/maturation in rats susceptible (Dark Agouti, DA) and relatively resistant (Albino Oxford, AO) to experimental autoimmune encephalomyelitis (EAE) induction was examined. Irrespective of strain, immunization for EAE (i) increased the circulating levels of IL-6, a cytokine causally linked with thymic atrophy, and (ii) led to thymic atrophy reflecting partly enhanced thymocyte apoptosis associated with downregulated thymic IL-7 expression. Additionally, immunization diminished the expression of Thy-1, a negative regulator of TCR alpha beta-mediated signaling and activation thresholds, on CD4+CD8+ TCR alpha beta(lo/hi) thymocytes undergoing selection and thereby impaired thymocyte selection/survival. This diminished the generation of mature CD4+ and CD8+ single positive TCR alpha beta(hi) thymocytes and, consequently, CD4+ and CD8+ recent thymic emigrants. In immunized rats, thymic differentiation of natural regulatory CD4+Foxp3+CD25+ T cells (nTregs) was particularly affected reflecting a diminished expression of IL-7, IL-2 and IL-15. The decline in the overall thymic T-cell output and nTreg generation was more pronounced in DA than AO rats. Additionally, differently from immunized AO rats, in DA ones the frequency of CD28- cells secreting cytolytic enzymes within peripheral blood CD4+ T lymphocytes increased, as a consequence of thymic atrophy-related replicative stress (mirrored in CD4+ cell memory pool expansion and p16(INK4a) accumulation). The higher circulating level of TNF-alpha in DA compared with AO rats could also contribute to this difference. Consistently, higher frequency of cytolytic CD4+ granzyme B+ cells (associated with greater tissue damage) was found in spinal cord of immunized DA rats compared with their AO counterparts. In conclusion, the study indicated that strain differences in immunization-induced changes in thymopoiesis and peripheral CD4+CD28- T-cell generation could contribute to rat strain-specific clinical outcomes of immunization for EAE.",
publisher = "Public Library Science, San Francisco",
journal = "PLoS One",
title = "Strain differences in thymic atrophy in rats immunized for EAE correlate with the clinical outcome of immunization",
volume = "13",
number = "8",
doi = "10.1371/journal.pone.0201848"
}
Nacka-Aleksić, M., Stojanović, M., Pilipović, I., Stojić-Vukanić, Z., Kosec, D.,& Leposavić, G.. (2018). Strain differences in thymic atrophy in rats immunized for EAE correlate with the clinical outcome of immunization. in PLoS One
Public Library Science, San Francisco., 13(8).
https://doi.org/10.1371/journal.pone.0201848
Nacka-Aleksić M, Stojanović M, Pilipović I, Stojić-Vukanić Z, Kosec D, Leposavić G. Strain differences in thymic atrophy in rats immunized for EAE correlate with the clinical outcome of immunization. in PLoS One. 2018;13(8).
doi:10.1371/journal.pone.0201848 .
Nacka-Aleksić, Mirjana, Stojanović, Marija, Pilipović, Ivan, Stojić-Vukanić, Zorica, Kosec, Duško, Leposavić, Gordana, "Strain differences in thymic atrophy in rats immunized for EAE correlate with the clinical outcome of immunization" in PLoS One, 13, no. 8 (2018),
https://doi.org/10.1371/journal.pone.0201848 . .
7
2
7

Strain specificities in age-related changes in mechanisms promoting and controlling rat spinal cord damage in experimental autoimmune encephalomyelitis

Stojić-Vukanić, Zorica; Pilipović, Ivan; Đikić, Jasmina; Vujnović, Ivana; Nacka-Aleksić, Mirjana; Bufan, Biljana; Arsenović-Ranin, Nevena; Kosec, Duško; Leposavić, Gordana

(Pergamon-Elsevier Science Ltd, Oxford, 2018)

TY  - JOUR
AU  - Stojić-Vukanić, Zorica
AU  - Pilipović, Ivan
AU  - Đikić, Jasmina
AU  - Vujnović, Ivana
AU  - Nacka-Aleksić, Mirjana
AU  - Bufan, Biljana
AU  - Arsenović-Ranin, Nevena
AU  - Kosec, Duško
AU  - Leposavić, Gordana
PY  - 2018
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3188
AB  - The study investigated strain specificities in age-related differences in CD8+ T cell-and microglial cell-mediated mechanisms implicated in induction/perpetuation and/or control of neuroinflammation in experimental autoimmune encephalomyelitis (EAE) in Albino Oxford (AO) and Dark Agouti (DA) rats exhibiting age-related changes in the susceptibility to EAE in the opposite direction (increase in relatively resistant AO rats vs decrease in DA rats). In the inductive phase of EAE, the greater number of fully differentiated effector CD8+ T lymphocytes was found in draining lymph nodes (dLNs) from aged rats of both strains than in strain-matched young rats, but this was particularly prominent in AO rats, which exhibited milder EAE of prolonged duration compared with their DA counterparts. Consistently, dLN IFN-gamma+ and IL-17+ CD8+ T cell counts were greater in aged AO than in DA rats. Additionally, the magnitudes of myelin basic protein (MBP)-induced rise in the frequency of IFN-gamma+ and IL-17+ CD8+ T cells (providing important help to neuroantigen-specific CD4+ T cells in EAE models characterized by clinically mild disease) were greater in dLN cell cultures from aged AO rats. Consistently, the magnitudes of MBP-induced rise in the frequency of both IFN-gamma+ and IL-17+ CD8+ T cells were greater in spinal cord mononuclear cell cultures from aged AO rats compared with their DA counterparts. Besides, with aging CD4+ CD25+ Foxp3+/CD8+ CD25+ Foxp3+ regulatory T cell ratio changed in spinal cord in the opposite direction. Consequently, in aged AO rats it was shifted towards CD8+ CD25+ Foxp3+ regulatory T cells (exhibiting lower suppressive capacity) when compared with DA rats. Moreover, the frequency of CX3CR1+ cells among microglia changed with aging and the disease development. In aged rats, in the effector phase of EAE it was lower in AO than in DA rats. This was accompanied by higher frequency of cells expressing IL-1 beta (whose down-regulation is central for CX3CR1-mediated neuroprotection), but lower that of phagocyting cells among microglia from aged AO compared their DA counterparts. The study indicates the control points linked with strain differences in age-related changes in EAE pathogenesis.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Experimental Gerontology
T1  - Strain specificities in age-related changes in mechanisms promoting and controlling rat spinal cord damage in experimental autoimmune encephalomyelitis
VL  - 101
SP  - 37
EP  - 53
DO  - 10.1016/j.exger.2017.11.002
ER  - 
@article{
author = "Stojić-Vukanić, Zorica and Pilipović, Ivan and Đikić, Jasmina and Vujnović, Ivana and Nacka-Aleksić, Mirjana and Bufan, Biljana and Arsenović-Ranin, Nevena and Kosec, Duško and Leposavić, Gordana",
year = "2018",
abstract = "The study investigated strain specificities in age-related differences in CD8+ T cell-and microglial cell-mediated mechanisms implicated in induction/perpetuation and/or control of neuroinflammation in experimental autoimmune encephalomyelitis (EAE) in Albino Oxford (AO) and Dark Agouti (DA) rats exhibiting age-related changes in the susceptibility to EAE in the opposite direction (increase in relatively resistant AO rats vs decrease in DA rats). In the inductive phase of EAE, the greater number of fully differentiated effector CD8+ T lymphocytes was found in draining lymph nodes (dLNs) from aged rats of both strains than in strain-matched young rats, but this was particularly prominent in AO rats, which exhibited milder EAE of prolonged duration compared with their DA counterparts. Consistently, dLN IFN-gamma+ and IL-17+ CD8+ T cell counts were greater in aged AO than in DA rats. Additionally, the magnitudes of myelin basic protein (MBP)-induced rise in the frequency of IFN-gamma+ and IL-17+ CD8+ T cells (providing important help to neuroantigen-specific CD4+ T cells in EAE models characterized by clinically mild disease) were greater in dLN cell cultures from aged AO rats. Consistently, the magnitudes of MBP-induced rise in the frequency of both IFN-gamma+ and IL-17+ CD8+ T cells were greater in spinal cord mononuclear cell cultures from aged AO rats compared with their DA counterparts. Besides, with aging CD4+ CD25+ Foxp3+/CD8+ CD25+ Foxp3+ regulatory T cell ratio changed in spinal cord in the opposite direction. Consequently, in aged AO rats it was shifted towards CD8+ CD25+ Foxp3+ regulatory T cells (exhibiting lower suppressive capacity) when compared with DA rats. Moreover, the frequency of CX3CR1+ cells among microglia changed with aging and the disease development. In aged rats, in the effector phase of EAE it was lower in AO than in DA rats. This was accompanied by higher frequency of cells expressing IL-1 beta (whose down-regulation is central for CX3CR1-mediated neuroprotection), but lower that of phagocyting cells among microglia from aged AO compared their DA counterparts. The study indicates the control points linked with strain differences in age-related changes in EAE pathogenesis.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Experimental Gerontology",
title = "Strain specificities in age-related changes in mechanisms promoting and controlling rat spinal cord damage in experimental autoimmune encephalomyelitis",
volume = "101",
pages = "37-53",
doi = "10.1016/j.exger.2017.11.002"
}
Stojić-Vukanić, Z., Pilipović, I., Đikić, J., Vujnović, I., Nacka-Aleksić, M., Bufan, B., Arsenović-Ranin, N., Kosec, D.,& Leposavić, G.. (2018). Strain specificities in age-related changes in mechanisms promoting and controlling rat spinal cord damage in experimental autoimmune encephalomyelitis. in Experimental Gerontology
Pergamon-Elsevier Science Ltd, Oxford., 101, 37-53.
https://doi.org/10.1016/j.exger.2017.11.002
Stojić-Vukanić Z, Pilipović I, Đikić J, Vujnović I, Nacka-Aleksić M, Bufan B, Arsenović-Ranin N, Kosec D, Leposavić G. Strain specificities in age-related changes in mechanisms promoting and controlling rat spinal cord damage in experimental autoimmune encephalomyelitis. in Experimental Gerontology. 2018;101:37-53.
doi:10.1016/j.exger.2017.11.002 .
Stojić-Vukanić, Zorica, Pilipović, Ivan, Đikić, Jasmina, Vujnović, Ivana, Nacka-Aleksić, Mirjana, Bufan, Biljana, Arsenović-Ranin, Nevena, Kosec, Duško, Leposavić, Gordana, "Strain specificities in age-related changes in mechanisms promoting and controlling rat spinal cord damage in experimental autoimmune encephalomyelitis" in Experimental Gerontology, 101 (2018):37-53,
https://doi.org/10.1016/j.exger.2017.11.002 . .
8
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8