TY - JOUR
T1 - T Cell Responses to the Microbiota
AU - Ivanov, Ivaylo I.
AU - Tuganbaev, Timur
AU - Skelly, Ashwin N.
AU - Honda, Kenya
N1 - Publisher Copyright:
© 2022 Annual Reviews Inc.. All rights reserved.
PY - 2022
Y1 - 2022
N2 - The immune system employs recognition tools to communicate with its microbial evolutionary partner. Among all the methods of microbial perception, T cells enable the widest spectrum of microbial recognition resolution, ranging from the crudest detection of whole groups of microbes to the finest detection of specific antigens. The application of this recognition capability to the crucial task of combatting infections has been the focus of classical immunology. We now appreciate that the coevolution of the immune system and the microbiota has led to development of a lush immunological decision tree downstream of microbial recognition, of which an inflammatory response is but one branch. In this review we discuss known T cell-microbe interactions in the gut and place them in the context of an algorithmic framework of recognition, context-dependent interpretation, and response circuits across multiple levels of microbial recognition resolution. The malleability of T cells in response to the microbiota presents an opportunity to edit immune response cellularity, identity, and functionality by utilizing microbiota-controlled pathways to promote human health.
AB - The immune system employs recognition tools to communicate with its microbial evolutionary partner. Among all the methods of microbial perception, T cells enable the widest spectrum of microbial recognition resolution, ranging from the crudest detection of whole groups of microbes to the finest detection of specific antigens. The application of this recognition capability to the crucial task of combatting infections has been the focus of classical immunology. We now appreciate that the coevolution of the immune system and the microbiota has led to development of a lush immunological decision tree downstream of microbial recognition, of which an inflammatory response is but one branch. In this review we discuss known T cell-microbe interactions in the gut and place them in the context of an algorithmic framework of recognition, context-dependent interpretation, and response circuits across multiple levels of microbial recognition resolution. The malleability of T cells in response to the microbiota presents an opportunity to edit immune response cellularity, identity, and functionality by utilizing microbiota-controlled pathways to promote human health.
KW - Th17 cells
KW - Tregs
KW - dendritic cells
KW - enteric nervous system
KW - intestinal microbiota
KW - segmented filamentous bacteria
KW - γδ T cells,MAIT cells
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U2 - 10.1146/annurev-immunol-101320-011829
DO - 10.1146/annurev-immunol-101320-011829
M3 - Review article
C2 - 35113732
AN - SCOPUS:85129778981
SN - 0732-0582
VL - 40
SP - 559
EP - 587
JO - Annual Review of Immunology
JF - Annual Review of Immunology
ER -