Regulation of T cells by gut commensal microbiota

被引:33
作者
Duan, Jinyou [1 ]
Kasper, Dennis L. [2 ,3 ]
机构
[1] NW A&F Univ, Coll Sci, Yangling 712100, Shaanxi, Peoples R China
[2] Brigham & Womens Hosp, Dept Med, Channing Lab, Boston, MA USA
[3] Harvard Univ, Sch Med, Dept Microbiol & Mol Genet, Boston, MA 02115 USA
关键词
allergy; arthritis; autoimmune disease; germ-free; gut flora; LAMINA PROPRIA; MAIT CELLS; INTRAEPITHELIAL LYMPHOCYTES; CYTOLYTIC ACTIVITY; IMMUNE-RESPONSES; NKT CELLS; BACTERIA; DRIVES; POLYSACCHARIDE; EXPRESSION;
D O I
10.1097/BOR.0b013e3283476d3e
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Purpose of review Commensal bacteria in the gut shape the innate and adaptive immune systems of the host. An understanding of how these microbes direct the development of various immune cells will unravel mechanisms underlying host-microbial interaction at the cellular level. In this review, we describe the impact of microbial colonization on the modulation of individual T-cell subsets in health and disease. Recent findings Compelling evidence demonstrates that the intestinal microbiota plays a pivotal role in the development of conventional and unconventional T cells both within and outside the intestine. Recent studies have documented an association of specific bacterial species with the development of certain T-cell subsets. Summary It is increasingly clear that specific components of the microbiota selectively expand and activate different T-cell subsets under normal and/or pathological conditions. Modulation of the complex microbiota may provide opportunities for the treatment of T-cell-mediated diseases.
引用
收藏
页码:372 / 376
页数:5
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