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dc.contributor.authorGharibi, T
dc.contributor.authorMajidi, J
dc.contributor.authorKazemi, T
dc.contributor.authorDehghanzadeh, R
dc.contributor.authorMotallebnezhad, M
dc.contributor.authorBabaloo, Z
dc.date.accessioned2018-08-26T07:31:08Z
dc.date.available2018-08-26T07:31:08Z
dc.date.issued2016
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/47199
dc.description.abstractInterleukin-21 (IL-21) is a member of the common gamma-chain cytokines with broad pleiotropic actions that affects different immune and nonimmune cells. IL-21 can affect differentiation, proliferation and function of T and B cells; it can also induce the maturation and enhance the cytotoxicity of CD8+ T cells and Natural killer (NK) cells. IL-21 exerts major effects on B-cell activation and differentiation or apoptosis during humoral immune responses and induces differentiation of naive B cells and memory B cells into plasma cells. IL-21 also affects different subtypes of T cells including T helper-17 (TH17), T follicular helper (TFH) and regulatory T (Treg) cells and thereby promotes the development of autoimmune disorders and inflammatory diseases. Observations have shown that the blockade of IL-21 has therapeutic effects on various autoimmune diseases in animal models. A better understanding of the regulation of cell differentiation and stabilization by IL-21 in the context of each specific autoimmune disease or tissue-specific pathological microenvironments will be helpful in developing novel treatments to control autoimmune diseases. Herein, we review the biological effects of IL-21 on different immune cells and uncover the emerging role of this interesting cytokine in autoimmune diseases. (C) 2015 Published by Elsevier GmbH.
dc.language.isoEnglish
dc.relation.ispartofIMMUNOBIOLOGY
dc.subjectInterleukin-21
dc.subjectAutoimmune diseases
dc.subjectCytokines
dc.titleBiological effects of IL-21 on different immune cells and its role in autoimmune diseases
dc.typeReview
dc.citation.volume221
dc.citation.issue2
dc.citation.spage357
dc.citation.epage367
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1016/j.imbio.2015.09.021


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