RIKEN Center for Integrative Medical Sciences (IMS), Yokohama, Kanagawa 230-0045, Japan.
Department of Microbiology and Immunology, Keio University School of Medicine, Tokyo 160-8582, Japan.
Nat Rev Immunol. 2016 May;16(5):295-309. doi: 10.1038/nri.2016.36. Epub 2016 Apr 18.
Gut-resident forkhead box P3 (FOXP3)(+)CD4(+) regulatory T cells (Treg cells) are distinct from those in other organs and have gut-specific phenotypes and functions. Whereas Treg cells in other organs have T cell receptors (TCRs) specific for self antigens, intestinal Treg cells have a distinct set of TCRs that are specific for intestinal antigens, and these cells have pivotal roles in the suppression of immune responses against harmless dietary antigens and commensal microorganisms. The differentiation, migration and maintenance of intestinal Treg cells are controlled by specific signals from the local environment. In particular, certain members of the microbiota continuously provide antigens and immunoregulatory small molecules that modulate intestinal Treg cells. Understanding the development and the maintenance of intestinal Treg cells provides important insights into disease-relevant host-microorganism interactions.
肠道驻留的叉头框 P3(FOXP3)(+)CD4(+)调节性 T 细胞(Treg 细胞)与其他器官中的 Treg 细胞不同,具有肠道特异性表型和功能。其他器官中的 Treg 细胞具有针对自身抗原的 T 细胞受体(TCR),而肠道 Treg 细胞具有一组特定于肠道抗原的 TCR,这些细胞在抑制针对无害膳食抗原和共生微生物的免疫反应中起关键作用。肠道 Treg 细胞的分化、迁移和维持受局部环境中特定信号的控制。特别是,某些微生物群成员不断提供抗原和免疫调节小分子,调节肠道 Treg 细胞。了解肠道 Treg 细胞的发育和维持为研究与疾病相关的宿主-微生物相互作用提供了重要的见解。
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