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Cellular targets of regulatory B cell-mediated suppression
被引:74
作者:
Rosser, Elizabeth C.
[1
]
Blair, Paul A.
[1
]
Mauri, Claudia
[1
]
机构:
[1] UCL, Ctr Rheumatol, Div Med, London WC1E 6JF, England
关键词:
Regulatory B cells;
Tolerance;
EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS;
SYSTEMIC-LUPUS-ERYTHEMATOSUS;
RENAL-TRANSPLANT TOLERANCE;
T-CELLS;
IMMUNE-RESPONSES;
DELAYED-HYPERSENSITIVITY;
IL-10;
PRODUCTION;
CUTTING EDGE;
BALB/C MICE;
INDUCTION;
D O I:
10.1016/j.molimm.2014.01.014
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Regulatory B cells (Bregs) are defined by their ability to restrain inflammatory responses both in vivo and in vitro. Interleukin 10 (IL-10) production by Bregs is thought to be central to their ability to regulate inflammation, largely due to IL-10s' ability to suppress pro-inflammatory cytokine production by effector lymphocytes and to maintain the differentiation of regulatory T cells (Tregs). However, with an increase in available published data, it has become evident that Bregs utilize a number of suppressive mechanisms in order to alter the activation of a variety of different lymphocytes. Here, we summarize the multiplicity of cellular targets of Breg-mediated suppression and describe the mechanisms employed by Bregs to suppress chronic inflammatory responses. (C) 2014 Elsevier Ltd. All rights reserved.
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页码:296 / 304
页数:9
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