Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/9036
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dc.rights.licenseBY-NC-ND-
dc.contributor.authorStojanovic B.-
dc.contributor.authorMilovanovic, Jelena-
dc.contributor.authorArsenijevic A.-
dc.contributor.authorMilovanovic, Marija-
dc.contributor.authorLukic, Miodrag-
dc.date.accessioned2020-09-19T17:18:18Z-
dc.date.available2020-09-19T17:18:18Z-
dc.date.issued2016-
dc.identifier.issn1820-8665-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/9036-
dc.description.abstract© 2016, University of Kragujevac, Faculty of Science, All rights reserved. B cells play a dual role in the pathogenesis of autoimmune diseases. In experimental autoimmune encephalomyelitis (EAE), an experimental model for multiple sclerosis, B cells contribute to disease progression, while their regulatory role predominates in the initial phases of disease development. Several studies have identified different subsets of regulatory B cells, mostly in the spleen, which are all sources of IL-10. However, peritoneal regulatory B cells are also important producers of IL-10, can migrate towards inflammatory stimuli, and could have an immunoregulatory function. As we have observed expansion of regulatory B cells in the peritoneum of resistant mice after EAE induction, herein we discuss the regulatory roles of B cells in EAE pathogenesis and the possible role of peritoneal regulatory B cells in resistance to EAE induction.-
dc.rightsopenAccess-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/-
dc.sourceSerbian Journal of Experimental and Clinical Research-
dc.titleRegulatory role of peritoneal B cells in EAE-
dc.typereview-
dc.identifier.doi10.1515/SJECR-2015-0048-
dc.identifier.scopus2-s2.0-84971009727-
Appears in Collections:Faculty of Medical Sciences, Kragujevac

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