4.7 Article Book Chapter

Induction of gut IgA production through T cell-dependent and T cell-independent pathways

期刊

YEAR IN IMMUNOLOGY
卷 1247, 期 -, 页码 97-116

出版社

BLACKWELL SCIENCE PUBL
DOI: 10.1111/j.1749-6632.2011.06378.x

关键词

IgA; commensal microbiota; B cell; class switch recombination; gut-associated lymphoid tissues

资金

  1. Wellcome Trust Funding Source: Medline

向作者/读者索取更多资源

The gut immune system protects against mucosal pathogens, maintains a mutualistic relationship with the microbiota, and establishes tolerance against food antigens. This requires a balance between immune effector responses and induction of tolerance. Disturbances of this strictly regulated balance can lead to infections or the development inflammatory diseases and allergies. Production of secretory IgA is a unique effector function at mucosal surfaces, and basal mechanisms regulating IgA production have been the focus of much recent research. These investigations have aimed at understanding how long-term IgA-mediated mucosal immunity can best be achieved by oral or sublingual vaccination, or at analyzing the relationship between IgA production, the composition of the gut microbiota, and protection from allergies and autoimmunity. This research has lead to a better understanding of the IgA system; but at the same time seemingly conflicting data have been generated. Here, we discuss how gut IgA production is controlled, with special focus on how differences between T cell-dependent and T cell-independent IgA production may explain some of these discrepancies.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据