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产生白细胞介素-17的T细胞的诱导、功能及调控

Induction, function and regulation of IL-17-producing T cells.

作者信息

Mills Kingston H G

机构信息

Immune Regulation Research Group, School of Biochemistry and Immunology, Trinity College, Dublin, Ireland.

出版信息

Eur J Immunol. 2008 Oct;38(10):2636-49. doi: 10.1002/eji.200838535.

Abstract

Recent reports have provided convincing evidence that IL-17-producing T cells play a key role in the pathogenesis of organ-specific autoimmune diseases, a function previously attributed exclusively to IFN-gamma-secreting Th1 cells. Furthermore, it appears that IL-17-producing T cells can also function with Th1 cells to mediate protective immunity to pathogens. Although much of the focus has been on IL-17-secreting CD4+ T cells, termed Th17 cells, CD8+ T cells, gammadelta T cells and NKT cells are also capable of secreting IL-17. The differentiation of Th17 cells from naïve T cells appears to involve signals from TGF-beta, IL-6, IL-21, IL-1beta and IL-23. Furthermore, IL-1alpha or IL-1beta in synergy with IL-23 can promote IL-17 secretion from memory T cells. The induction or function of Th17 cells is regulated by cytokines secreted by the other major subtypes of T cells, including IFN-gamma, IL-4, IL-10 and at high concentrations, TGF-beta. The main function of IL-17-secreting T cells is to mediate inflammation, by stimulating production of inflammatory cytokines, such as TNF-alpha, IL-1beta and IL-6, and inflammatory chemokines that promote the recruitment of neutrophils and macrophages.

摘要

最近的报告提供了令人信服的证据,表明产生白细胞介素-17(IL-17)的T细胞在器官特异性自身免疫性疾病的发病机制中起关键作用,这一功能以前仅归因于分泌干扰素-γ(IFN-γ)的Th1细胞。此外,产生IL-17的T细胞似乎还能与Th1细胞共同作用,介导对病原体的保护性免疫。尽管大部分研究重点都放在了分泌IL-17的CD4+T细胞(即Th17细胞)上,但CD8+T细胞、γδT细胞和自然杀伤T细胞(NKT细胞)也能够分泌IL-17。幼稚T细胞向Th17细胞的分化似乎涉及转化生长因子-β(TGF-β)、白细胞介素-6(IL-6)、白细胞介素-21(IL-21)、白细胞介素-1β(IL-1β)和白细胞介素-23(IL-23)发出的信号。此外,IL-1α或IL-1β与IL-23协同作用可促进记忆T细胞分泌IL-17。Th17细胞的诱导或功能受其他主要T细胞亚群分泌的细胞因子调节,包括IFN-γ、IL-4、IL-10以及高浓度的TGF-β。分泌IL-17的T细胞的主要功能是通过刺激炎性细胞因子(如肿瘤坏死因子-α(TNF-α)、IL-1β和IL-6)以及促进中性粒细胞和巨噬细胞募集的炎性趋化因子的产生来介导炎症。

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