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Review
. 2020 Dec 15:2020:8813558.
doi: 10.1155/2020/8813558. eCollection 2020.

"V体育安卓版" The Function and Role of the Th17/Treg Cell Balance in Inflammatory Bowel Disease

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Review

The Function and Role of the Th17/Treg Cell Balance in Inflammatory Bowel Disease

"V体育平台登录" Jun-Bin Yan et al. J Immunol Res. .

Abstract

Inflammatory bowel disease (IBD) is a chronic, inflammatory, and autoimmune disorder. The pathogenesis of IBD is not yet clear. Studies have shown that the imbalance between T helper 17 (Th17) and regulatory T (Treg) cells, which differentiate from CD4+ T cells, contributes to IBD VSports手机版. Th17 cells promote tissue inflammation, and Treg cells suppress autoimmunity in IBD. Therefore, Th17/Treg cell balance is crucial. Some regulatory factors affecting the production and maintenance of these cells are also important for the proper regulation of the Th17/Treg balance; these factors include T cell receptor (TCR) signaling, costimulatory signals, cytokine signaling, bile acid metabolites, and the intestinal microbiota. This article focuses on our understanding of the function and role of the balance between Th17/Treg cells in IBD and these regulatory factors and their clinical significance in IBD. .

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Conflict of interest statement

The authors declare that they have no conflicts of interest.

Figures

Figure 1
Figure 1
The role of bile acid and bile acid receptor FXR/TGR5 agonist in Th17/Treg balance.
Figure 2
Figure 2
The role of intestinal microbiota in Th17/Treg balance.

References

    1. Molodecky N. A., Soon I. S., Rabi D. M., et al. Increasing incidence and prevalence of the inflammatory bowel diseases with time, based on systematic review. Gastroenterology. 2012;142(1):46–54.e42. doi: 10.1053/j.gastro.2011.10.001. - DOI - PubMed
    1. Ananthakrishnan A. N. Epidemiology and risk factors for IBD. Nature Reviews Gastroenterology & Hepatology. 2015;12(4):205–217. doi: 10.1038/nrgastro.2015.34. - DOI - PubMed
    1. Ananthakrishnan A. N., Bernstein C. N., Iliopoulos D., et al. Environmental triggers in IBD: a review of progress and evidence. Nature Reviews Gastroenterology & Hepatology. 2018;15(1):39–49. doi: 10.1038/nrgastro.2017.136. - DOI - PubMed
    1. Iacomino G., Rotondi Aufiero V., Iannaccone N., et al. IBD: role of intestinal compartments in the mucosal immune response. Immunobiology. 2020;225(1, article 151849) doi: 10.1016/j.imbio.2019.09.008. - DOI - PubMed
    1. Silva F. A., Rodrigues B. L., Ayrizono M. L., Leal R. F. The immunological basis of inflammatory bowel disease. Gastroenterology research and practice. 2016;2016:11. doi: 10.1155/2016/2097274.2097274 - DOI - PMC - PubMed

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