The regulation of gut mucosal IgA B-cell responses: recent developments

被引:136
作者
Lycke, N. Y. [1 ]
Bemark, M. [1 ]
机构
[1] Univ Gothenburg, Inst Biomed, Dept Microbiol & Immunol, Mucosal Immunobiol & Vaccine Ctr, Gothenburg, Sweden
基金
瑞典研究理事会;
关键词
CLASS SWITCH RECOMBINATION; SEGMENTED FILAMENTOUS BACTERIA; FOLLICULAR HELPER-CELLS; IMMUNOGLOBULIN-A GENERATION; CHOLERA ANTITOXIN MEMORY; CD103(+) DENDRITIC CELLS; CYTIDINE DEAMINASE AID; FOXP3(+) T-CELLS; FACTOR SPI-B; INTESTINAL IGA;
D O I
10.1038/mi.2017.62
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The majority of activated B cells differentiate into IgA plasma cells, with the gut being the largest producer of immunoglobulin in the body. Secretory IgA antibodies have numerous critical functions of which protection against infections and the role for establishing a healthy microbiota appear most important. Expanding our knowledge of the regulation of IgA B-cell responses and how effective mucosal vaccines can be designed are of critical importance. Here we discuss recent developments in the field that shed light on the uniqueness and complexity of mucosal IgA responses and the control of protective IgA responses in the gut, specifically.
引用
收藏
页码:1361 / 1374
页数:14
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