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T helper 17 (Th17) cell responses to the gut microbiota in human diseases.

Authors :
Sun, Chao-Yue
Yang, Na
Zheng, Zuo-Liang
Liu, Dong
Xu, Qi-Lin
Source :
Biomedicine & Pharmacotherapy. May2023, Vol. 161, pN.PAG-N.PAG. 1p.
Publication Year :
2023

Abstract

The gut microbiota colonizing the gastrointestinal tract, is an indispensable "invisible organ" that affects multiple aspects of human health. The gut microbial community has been assumed to be an important stimulus to the immune homeostasis and development, and increasing data support the role of the gut microbiota-immunity axis in autoimmune diseases. Host's immune system requires recognition tools to communicate with the gut microbial evolutionary partners. Among these microbial perceptions, T cells enable the widest spectrum of gut microbial recognition resolution. Specific gut microbiota direct the induction and differentiation of Th17 cells in intestine. However, the detailed links between the gut microbiota and Th17 cells have not been well established. In this review, we describe the generation and characterization of Th17 cells. Notably, we discuss the induction and differentiation of Th17 cells by the gut microbiota and their metabolites, as well as recent advances in our understanding of interactions between Th17 cells and the gut microbiota in human diseases. In addition, we provide the emerging evidences in support of interventions targeting the gut microbes/Th17 cells in human diseases. [Display omitted] ● Th17 cells are clinically correlated with the gut microbiota in human diseases. ● The gut microbiota and their metabolites trigger the induction and differentiation of Th17 cells. ● The gut microbiota can interact with Th17 cells in human diseases. ● The interactions between the gut microbiota and Th17 cells provide opportunities to improve human diseases. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
07533322
Volume :
161
Database :
Academic Search Index
Journal :
Biomedicine & Pharmacotherapy
Publication Type :
Academic Journal
Accession number :
162759875
Full Text :
https://doi.org/10.1016/j.biopha.2023.114483