
CLC number:
On-line Access: 2026-01-27
Received: 2024-08-20
Revision Accepted: 2025-01-05
Crosschecked: 2026-01-27
Cited: 0
Clicked: 2123
Citations: Bibtex RefMan EndNote GB/T7714
https://orcid.org/0009-0006-5440-9954
https://orcid.org/0000-0002-6666-9546
Shuyu TU, Yanan ZHANG, Li ZHANG, Shu Jeffrey ZHU. Commensal bacteria play a fundamental role in maintaining gut immune homeostasis[J]. Journal of Zhejiang University Science B, 2026, 27(1): 101-104.
@article{title="Commensal bacteria play a fundamental role in maintaining gut immune homeostasis",
author="Shuyu TU, Yanan ZHANG, Li ZHANG, Shu Jeffrey ZHU",
journal="Journal of Zhejiang University Science B",
volume="27",
number="1",
pages="101-104",
year="2026",
publisher="Zhejiang University Press & Springer",
doi="10.1631/jzus.B2400431"
}
%0 Journal Article
%T Commensal bacteria play a fundamental role in maintaining gut immune homeostasis
%A Shuyu TU
%A Yanan ZHANG
%A Li ZHANG
%A Shu Jeffrey ZHU
%J Journal of Zhejiang University SCIENCE B
%V 27
%N 1
%P 101-104
%@ 1673-1581
%D 2026
%I Zhejiang University Press & Springer
%DOI 10.1631/jzus.B2400431
TY - JOUR
T1 - Commensal bacteria play a fundamental role in maintaining gut immune homeostasis
A1 - Shuyu TU
A1 - Yanan ZHANG
A1 - Li ZHANG
A1 - Shu Jeffrey ZHU
J0 - Journal of Zhejiang University Science B
VL - 27
IS - 1
SP - 101
EP - 104
%@ 1673-1581
Y1 - 2026
PB - Zhejiang University Press & Springer
ER -
DOI - 10.1631/jzus.B2400431
Abstract: The intestinal microbiome, which is a key factor in the maintenance of host gut homeostasis, enhances intestinal mucosal barrier function and immune tolerance (Rooks and Garrett, 2016; Skelly et al., 2019). However, the specific immunomodulatory functions of microbiota-derived metabolites in mucosal inflammatory responses remain largely unknown. The effects of microbial metabolites may vary across different immune cell types and host homeostasis (Hu et al., 2023; Zhao et al., 2023). Hence, it is fundamental to understand how specific intestinal microbes and their metabolic small molecules cause or mitigate gut-related diseases like inflammatory bowel disease (IBD). It has been uncovered that during the pathogenesis of IBD, excessive T helper 1 cell (Th1)/Th17 activation and impaired function of colonic regulatory T cells (Tregs) occur (Subramanian, 2020). Given that colonic Tregs play an important role in inhibiting IBD via secreting immunosuppressive cytokines, the molecular mechanisms linking certain intestinal microbes and their metabolites to Treg-mediated immune tolerance are yet to be fully understood.
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