Regulation of inflammation by microbiota interactions with the host

被引:482
作者
Blander, J. Magarian [1 ,2 ,3 ]
Longman, Randy S. [1 ,2 ]
Iliev, Iliyan D. [1 ,2 ]
Sonnenberg, Gregory F. [1 ,2 ,3 ]
Artis, David [1 ,2 ,3 ]
机构
[1] Cornell Univ, Jill Roberts Inst Res Inflammatory Bowel Dis, Joan & Sanford I Weill Dept Med, Weill Cornell Med, New York, NY 10021 USA
[2] Cornell Univ, Dept Microbiol & Immunol, Weill Cornell Med, New York, NY 10021 USA
[3] Cornell Univ, Sandra & Edward Meyer Canc Ctr, Weill Cornell Med, New York, NY 10021 USA
关键词
ARYL-HYDROCARBON RECEPTOR; CHAIN FATTY-ACIDS; T-CELL RESPONSES; INNATE LYMPHOID-CELLS; HUMAN GUT MICROBIOTA; COMMENSAL BACTERIA; INTESTINAL MICROBIOTA; BOWEL-DISEASE; CROHNS-DISEASE; IMMUNE HOMEOSTASIS;
D O I
10.1038/ni.3780
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 study of the intestinal microbiota has begun to shift from cataloging individual members of the commensal community to understanding their contributions to the physiology of the host organism in health and disease. Here, we review the effects of the microbiome on innate and adaptive immunological players from epithelial cells and antigen-presenting cells to innate lymphoid cells and regulatory T cells. We discuss recent studies that have identified diverse microbiota-derived bioactive molecules and their effects on inflammation within the intestine and distally at sites as anatomically remote as the brain. Finally, we highlight new insights into how the microbiome influences the host response to infection, vaccination and cancer, as well as susceptibility to autoimmune and neurodegenerative disorders.
引用
收藏
页码:851 / 860
页数:10
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