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视黄酸介导的TH17细胞与调节性T细胞的相互分化

Reciprocal TH17 and regulatory T cell differentiation mediated by retinoic acid.

作者信息

Mucida Daniel, Park Yunji, Kim Gisen, Turovskaya Olga, Scott Iain, Kronenberg Mitchell, Cheroutre Hilde

机构信息

La Jolla Institute for Allergy and Immunology, 9420 Athena Circle, La Jolla, CA 92037, USA.

出版信息

Science. 2007 Jul 13;317(5835):256-60. doi: 10.1126/science.1145697. Epub 2007 Jun 14.

Abstract

The cytokine transforming growth factor-beta (TGF-beta) converts naïve T cells into regulatory T (Treg) cells that prevent autoimmunity. However, in the presence of interleukin-6 (IL-6), TGF-beta has also been found to promote the differentiation of naïve T lymphocytes into proinflammatory IL-17 cytokine-producing T helper 17 (T(H)17) cells, which promote autoimmunity and inflammation. This raises the question of how TGF-beta can generate such distinct outcomes. We identified the vitamin A metabolite retinoic acid as a key regulator of TGF-beta-dependent immune responses, capable of inhibiting the IL-6-driven induction of proinflammatory T(H)17 cells and promoting anti-inflammatory Treg cell differentiation. These findings indicate that a common metabolite can regulate the balance between pro- and anti-inflammatory immunity.

摘要

细胞因子转化生长因子-β(TGF-β)可将初始T细胞转化为调节性T(Treg)细胞,从而预防自身免疫。然而,在白细胞介素-6(IL-6)存在的情况下,人们还发现TGF-β可促进初始T淋巴细胞分化为产生促炎细胞因子白细胞介素-17的辅助性T细胞17(TH17),后者会促进自身免疫和炎症。这就引出了一个问题,即TGF-β如何能产生如此不同的结果。我们确定视黄酸这种维生素A代谢产物是TGF-β依赖性免疫反应的关键调节因子,它能够抑制IL-6驱动的促炎性TH17细胞的诱导,并促进抗炎性Treg细胞的分化。这些发现表明,一种常见的代谢产物可以调节促炎免疫和抗炎免疫之间的平衡。

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