Immune Regulatory Function of B Cells

被引:944
作者
Mauri, Claudia [1 ]
Bosma, Anneleen [1 ]
机构
[1] UCL, Ctr Rheumatol Res, Div Med, London WC1E 6JF, England
来源
ANNUAL REVIEW OF IMMUNOLOGY, VOL 30 | 2012年 / 30卷
关键词
interleukin-10; suppressor B cell; immune-related disease; tolerance; B cell differentiation; SYSTEMIC-LUPUS-ERYTHEMATOSUS; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; RENAL-TRANSPLANT TOLERANCE; NONOBESE DIABETIC MICE; IN-VIVO PRODUCTION; T-CELLS; RHEUMATOID-ARTHRITIS; DEPLETION THERAPY; B10; CELLS; DELAYED-HYPERSENSITIVITY;
D O I
10.1146/annurev-immunol-020711-074934
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
B cells are regarded for their capacity to produce antibody. However, recent advances in B cell biology have capitalized on old findings and demonstrated that B cells also release a broad variety of cytokines. As with T helper cells, B cells can be classified into subsets according to the cytokine milieu that they produce. One functional B cell subset, regulatory B cells (Bregs), has recently been shown to contribute to the maintenance of the fine equilibrium required for tolerance. Bregs restrain the excessive inflammatory responses that occur during autoimmune diseases or that can be caused by unresolved infections. Pivotal to Breg function is interleukin-10 (IL-10), which inhibits proinflammatory cytokines and supports regulatory T cell differentiation. This review reports and discusses the factors that are important for Breg differentiation and for their effector function in both mouse and human.
引用
收藏
页码:221 / 241
页数:21
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