Integration of B cell responses through Toll-like receptors and antigen receptors

被引:266
作者
Rawlings, David J. [1 ,2 ,3 ]
Schwartz, Marc A. [2 ,3 ]
Jackson, Shaun W. [1 ,3 ]
Meyer-Bahlburg, Almut [4 ]
机构
[1] Univ Washington, Sch Med, Dept Pediat, Seattle, WA 98195 USA
[2] Univ Washington, Sch Med, Dept Immunol, Seattle, WA 98195 USA
[3] Seattle Childrens Res Inst, Ctr Immun & Immunotherapies, Seattle, WA 98101 USA
[4] Hannover Med Sch, Dept Pediat Pneumol & Neonatol, D-3000 Hannover, Germany
基金
美国国家卫生研究院;
关键词
SYSTEMIC-LUPUS-ERYTHEMATOSUS; COMMON VARIABLE IMMUNODEFICIENCY; PYOGENIC BACTERIAL-INFECTIONS; CLASS SWITCH RECOMBINATION; SPLENIC MARGINAL ZONE; INNATE IMMUNITY; TLR SIGNALS; T-CELLS; STREPTOCOCCUS-PNEUMONIAE; TRANSMEMBRANE ACTIVATOR;
D O I
10.1038/nri3190
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
Unlike other immune cells, B cells express both an antigen-specific B cell receptor (BCR) and Toll-like receptors (TLRs). Dual BCR and TLR engagement can fine-tune functional B cell responses, directly linking cell-intrinsic innate and adaptive immune programmes. Although most data regarding B cell-specific functions of the TLR signalling pathway have been obtained in mice, the discovery of patients with a deficiency in this pathway has recently provided an insight into human B cell responses. Here, we highlight the importance of the integration of signalling pathways downstream of BCRs and TLRs in modulating B cell function, focusing when possible on B cell-intrinsic roles.
引用
收藏
页码:282 / 294
页数:13
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