Control of Immunity by the Microbiota

被引:163
作者
Ansaldo, Eduard [1 ]
Farley, Taylor K. [1 ,2 ]
Belkaid, Yasmine [1 ,3 ]
机构
[1] NIAID, Metaorganism Immun Sect, Lab Host Immun & Microbiome, Bethesda, MD 20814 USA
[2] Univ Oxford, Nuffield Dept Orthopaed Rheumatol & Musculoskelet, Kennedy Inst Rheumatol, Oxford OX3 7FY, England
[3] NIAID, Microbiome Program, Bethesda, MD 20892 USA
来源
ANNUAL REVIEW OF IMMUNOLOGY, VOL 39 | 2021年 / 39卷
关键词
microbiota; barrier tissue; immunity; T cell; B cell; antibodies; unconventional T cell; REGULATORY T-CELLS; SEGMENTED FILAMENTOUS BACTERIA; DELTA INTRAEPITHELIAL LYMPHOCYTES; MUCOSAL IGA RESPONSES; GERM-FREE MICE; COMMENSAL-BACTERIA; GUT MICROBIOTA; SYMBIOTIC BACTERIA; IMMUNOGLOBULIN-A; EARLY-LIFE;
D O I
10.1146/annurev-immunol-093019-112348
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 immune system has coevolved with extensive microbial communities living on barrier sites that are collectively known as the microbiota. It is increasingly clear that microbial antigens and metabolites engage in a constant dialogue with the immune system, leading to microbiota-specific immune responses that occur in the absence of inflammation. This form of homeostatic immunity encompasses many arms of immunity, including B cell responses, innate-like T cells, and conventional T helper and T regulatory responses. In this review we summarize known examples of innate-like T cell and adaptive immunity to the microbiota, focusing on fundamental aspects of commensal immune recognition across different barrier sites. Furthermore, we explore how this cross talk is established during development, emphasizing critical temporal windows that establish long-term immune function. Finally, we highlight how dysregulation of immunity to the microbiota can lead to inflammation and disease, and we pinpoint outstanding questions and controversies regarding immune system-microbiota interactions.
引用
收藏
页码:449 / 479
页数:31
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