Innate control of B cell responses

被引:83
作者
Cerutti, Andrea [1 ,2 ]
Puga, Irene [2 ]
Cols, Montserrat [3 ]
机构
[1] Catalan Inst Res & Adv Studies, ICREA, Barcelona 08003, Spain
[2] Hosp del Mar, IMIM, Barcelona 08003, Spain
[3] Mt Sinai Sch Med, Dept Med, Inst Immunol, New York, NY 10029 USA
基金
美国国家卫生研究院;
关键词
CLASS-SWITCH RECOMBINATION; COMMON VARIABLE IMMUNODEFICIENCY; PYOGENIC BACTERIAL-INFECTIONS; IMMUNOGLOBULIN-A GENERATION; TOLL-LIKE RECEPTORS; NF-KAPPA-B; DENDRITIC CELLS; SOMATIC HYPERMUTATION; TRANSMEMBRANE ACTIVATOR; BAFF-R;
D O I
10.1016/j.it.2011.02.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mature B cells generate protective immunity by undergoing immunoglobulin (Ig) class switching and somatic hypermutation, two Ig gene-diversifying processes that usually require cognate interactions with T cells that express CD40 ligand. This T cell-dependent pathway provides immunological memory but is relatively slow to occur. Thus, it must be integrated with a faster, T cell-independent pathway for B cell activation through CD40 ligand-like molecules that are released by innate immune cells in response to microbial products. Here, we discuss recent advances in our understanding of the interplay between the innate immune system and B cells, particularly at the mucosa! interface. We also review the role of innate signals in the regulation of Ig diversification and production
引用
收藏
页码:202 / 211
页数:10
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