上皮内淋巴细胞
生物
免疫系统
拟杆菌
免疫学
效应器
微生物群
共生
抗原
归巢(生物学)
炎症
微生物学
CD8型
细胞生物学
细菌
遗传学
生态学
16S核糖体RNA
作者
Djenet Bousbaine,Laura Fisch,Mariya London,Preksha Bhagchandani,Tiago B. R. Castro,Mark Mimee,Scott W. Olesen,Bernardo Sgarbi Reis,David VanInsberghe,Juliana Bortolatto,Mathilde Poyet,Ross W. Cheloha,John Sidney,Jingjing Ling,Aaron Gupta,Timothy K. Lu,Alessandro Sette,Eric J. Alm,James J. Moon,Gabriel D. Victora
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2022-08-04
卷期号:377 (6606): 660-666
被引量:69
标识
DOI:10.1126/science.abg5645
摘要
The microbiome contributes to the development and maturation of the immune system. In response to commensal bacteria, intestinal CD4+ T lymphocytes differentiate into functional subtypes with regulatory or effector functions. The development of small intestine intraepithelial lymphocytes that coexpress CD4 and CD8αα homodimers (CD4IELs) depends on the microbiota. However, the identity of the microbial antigens recognized by CD4+ T cells that can differentiate into CD4IELs remains unknown. We identified β-hexosaminidase, a conserved enzyme across commensals of the Bacteroidetes phylum, as a driver of CD4IEL differentiation. In a mouse model of colitis, β-hexosaminidase-specific lymphocytes protected against intestinal inflammation. Thus, T cells of a single specificity can recognize a variety of abundant commensals and elicit a regulatory immune response at the intestinal mucosa.
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