Microbiota-Mediated Inflammation and Antimicrobial Defense in the Intestine

被引:198
作者
Caballero, Silvia [1 ]
Pamer, Eric G. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Program Immunol, Sloan Kettering Inst, Infect Dis Serv, New York, NY 10065 USA
来源
ANNUAL REVIEW OF IMMUNOLOGY VOL 33 | 2015年 / 33卷
基金
美国国家卫生研究院;
关键词
commensals; mucins; TLR signaling; antimicrobial molecules; dendritic cells; INNATE LYMPHOID-CELLS; SEGMENTED FILAMENTOUS BACTERIA; HUMAN GUT MICROBIOTA; PLASMACYTOID DENDRITIC CELLS; DEPENDENT MUCUS LAYERS; LECTIN REGIII-GAMMA; REGULATORY T-CELLS; COMMENSAL BACTERIA; RETINOIC-ACID; ANTIBIOTIC-TREATMENT;
D O I
10.1146/annurev-immunol-032713-120238
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
The diverse microbial populations constituting the intestinal microbiota promote immune development and differentiation, but because of their complex metabolic requirements and the consequent difficulty culturing them, they remained, until recently, largely uncharacterized and mysterious. In the last decade, deep nucleic acid sequencing platforms, new computational and bioinformatics tools, and full-genome characterization of several hundred commensal bacterial species facilitated studies of the microbiota and revealed that differences in microbiota composition can be associated with inflammatory, metabolic, and infectious diseases, that each human is colonized by a distinct bacterial flora, and that the microbiota can be manipulated to reduce and even cure some diseases. Different bacterial species induce distinct immune cell populations that can play pro- and anti-inflammatory roles, and thus the composition of the microbiota determines, in part, the level of resistance to infection and susceptibility to inflammatory diseases. This review summarizes recent work characterizing commensal microbes that contribute to the antimicrobial defense/inflammation axis.
引用
收藏
页码:227 / 256
页数:30
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