4.6 Review

Interleukin 35: Critical regulator of immunity and lymphocyte-mediated diseases

期刊

CYTOKINE & GROWTH FACTOR REVIEWS
卷 26, 期 5, 页码 587-593

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.cytogfr.2015.07.013

关键词

Interleukin 35; IL-12 family cytokines; Autoimmune diseases; Cytokine therapy; Regulatory B cells; Breg; i35-Breg; iTR35; Adoptive B cell therapy

资金

  1. Intramural NIH HHS [Z01 EY000262-13, ZIA EY000372-14, ZIA EY000262-19, ZIA EY000315-21] Funding Source: Medline

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Cytokines coordinate the activities of innate and adaptive immune systems and the Interleukin 12 (IL-12) family of cytokines has emerged as critical regulators of immunity in infectious and autoimmune diseases. While some members (IL-12 and IL-23) are associated with the pathogenesis of chronic inflammatory diseases, others (IL-27 and IL-35) mitigate autoimmune diseases. Unlike IL-12, IL-23 and IL-27 that are produced mainly by antigen presenting cells, IL-35 is predominantly secreted by regulatory B (i35-Bregs) and T (iTR35) cells. The discovery that IL-35 can induce the conversion or expansion of lymphocytes to regulatory B and T cells has considerable implications for therapeutic use of autologous regulatory B and T cells in human diseases. Although our current understanding of the immunobiology of IL-35 or its subunits (p35 and Ebi3) is still rudimentary, our goal in this review is to summarize what we know about this enigmatic cytokine and its potential clinical use, particularly in the treatment of CNS autoimmune diseases. Published by Elsevier Ltd.

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