IgA Responses to Microbiota

被引:307
作者
Bunker, Jeffrey J. [1 ,2 ]
Bendelac, Albert [1 ,2 ]
机构
[1] Univ Chicago, Comm Immunol, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Pathol, 5841 S Maryland Ave, Chicago, IL 60637 USA
关键词
SEGMENTED FILAMENTOUS BACTERIA; SECRETORY IMMUNOGLOBULIN-A; MEMORY B-CELLS; CLASS SWITCH RECOMBINATION; MUCOSAL IMMUNE-SYSTEM; FOXP3(+) T-CELLS; FC-ALPHA-RI; PLASMA-CELLS; PEYERS-PATCHES; GUT IGA;
D O I
10.1016/j.immuni.2018.08.011
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
Various immune mechanisms are deployed in the mucosa to confront the immense diversity of resident bacteria. A substantial fraction of the commensal microbiota is coated with immunoglobulin A (IgA) antibodies, and recent findings have established the identities of these bacteria under homeostatic and disease conditions. Here we review the current understanding of IgA biology, and present a framework wherein two distinct types of humoral immunity coexist in the gastrointestinal mucosa. Homeostatic IgA responses employ a polyreactive repertoire to bind a broad but taxonomically distinct subset of microbiota. In contrast, mucosal pathogens and vaccines elicit high-affinity, T cell-dependent antibody responses. This model raises fundamental questions including how polyreactive IgA specificities are generated, how these antibodies exert effector functions, and how they exist together with other immune responses during homeostasis and disease.
引用
收藏
页码:211 / 224
页数:14
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