A conserved Bacteroidetes antigen induces anti-inflammatory intestinal T lymphocytes

Djenet Bousbaine(Boston Children's Hospital), Laura Fisch(Boston Children's Hospital), Mariya London(Rockefeller University), Preksha Bhagchandani(Boston Children's Hospital), Tiago B. R. Castro(Rockefeller University), Mark Mimee(IIT@MIT), Scott W. Olesen(IIT@MIT), Bernardo Sgarbi Reis(Rockefeller University), David VanInsberghe(IIT@MIT), Juliana Bortolatto(Rockefeller University), Mathilde Poyet(IIT@MIT), Ross W. Cheloha(Boston Children's Hospital), John Sidney(La Jolla Institute for Immunology), Jingjing Ling(Boston Children's Hospital), Aaron Gupta(Rockefeller University), Timothy K. Lu(IIT@MIT), Alessandro Sette(La Jolla Institute for Immunology), Eric J. Alm(IIT@MIT), James J. Moon(Massachusetts General Hospital), Gabriel D. Victora(Rockefeller University), Daniel Mucida(Howard Hughes Medical Institute), Hidde L. Ploegh(Boston Children's Hospital), Angelina M. Bilate(Rockefeller University)
Science
August 4, 2022
Cited by 100Open Access
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Abstract

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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