Emerging roles for antigen presentation in establishing host-microbiome symbiosis

被引:19
作者
Bessman, Nicholas J. [1 ,2 ,3 ]
Sonnenberg, Gregory F. [1 ,2 ,3 ]
机构
[1] Weill Cornell Med, Div Gastroenterol, Joan & Sanford I Weill Dept Med, New York, NY USA
[2] Weill Cornell Med, Dept Microbiol & Immunol, New York, NY USA
[3] Weill Cornell Med, Jill Roberts Inst Res Inflammatory Bowel Dis, New York, NY USA
基金
美国国家卫生研究院;
关键词
IL-22; IgA; microbiota; innate lymphoid cells; bacterial infection; INNATE LYMPHOID-CELLS; ROR-GAMMA-T; COMMENSAL BACTERIA; DENDRITIC CELLS; INTESTINAL INFLAMMATION; GUT MICROBIOTA; COLONIZATION RESISTANCE; SECRETORY ANTIBODIES; EPITHELIAL-CELLS; IGA RESPONSES;
D O I
10.1111/imr.12425
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Trillions of beneficial bacteria inhabit the intestinal tract of healthy mammals from birth. Accordingly, mammalian hosts have evolved a series of complementary and redundant pathways to limit pathologic immune responses against these bacteria, while simultaneously protecting against enteric pathogen invasion. These pathways can be generically responsive to the presence of any commensal bacteria and innate in nature, as for IL-22-related pathways. Alternatively, specific bacterial antigens can drive a distinct set of adaptive immune cell responses, including IgA affinity maturation and secretion, and a recently described pathway of intestinal selection whereby MHCII+ ILC3 deletes commensal bacteria-reactive CD4 T cells. These pathways can either promote or inhibit colonization by specific subsets of commensal bacteria, and cooperatively maintain intestinal homeostasis. In this review, we will highlight recent developments in understanding how these diverse pathways complement each other to cooperatively shape the symbiotic relationship between commensal bacteria and mammalian hosts.
引用
收藏
页码:139 / 150
页数:12
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