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自身免疫中的CD8 + T细胞。

CD8+ T cells in autoimmunity.

作者信息

Walter Ulrich, Santamaria Pere

机构信息

Julia McFarlane Diabetes Research Centre and Department of Microbiology and Infectious Diseases, Faculty of Medicine, The University of Calgary, 3330 Hospital Drive NW, Calgary, Alberta T2N 4N1, Canada.

出版信息

Curr Opin Immunol. 2005 Dec;17(6):624-31. doi: 10.1016/j.coi.2005.09.014. Epub 2005 Oct 13.

Abstract

Mounting evidence shows that CD8(+) T cells contribute to the initiation, progression and regulation of several pathogenic autoimmune responses in which these cells were not previously thought to play a major role. CD8(+) T cells can kill target cells directly, by recognizing peptide-MHC complexes on target cells, or indirectly, by secreting cytokines capable of signaling through death receptors expressed on the target cell surface. Autoreactive CD8(+) T cells can also contribute to autoimmunity by releasing cytokines capable of increasing the susceptibility of target cells to cytotoxicity, or by secreting chemokines that attract other immune cells to the site of autoimmunity. Autoreactive CD8(+) T cells can also downregulate autoimmune responses. Recent important advances include a mechanistic understanding of events leading to the activation and recruitment of autoreactive CD8(+) T cells in certain autoimmune responses and a greater appreciation of the diverse roles that these T cells play in autoimmunity.

摘要

越来越多的证据表明,CD8(+) T细胞在几种致病性自身免疫反应的起始、进展和调节中发挥作用,而这些细胞以前被认为在其中不发挥主要作用。CD8(+) T细胞可以通过识别靶细胞上的肽-MHC复合物直接杀死靶细胞,也可以通过分泌能够通过靶细胞表面表达的死亡受体发出信号的细胞因子间接杀死靶细胞。自身反应性CD8(+) T细胞还可以通过释放能够增加靶细胞对细胞毒性敏感性的细胞因子,或通过分泌吸引其他免疫细胞到自身免疫部位的趋化因子来促进自身免疫。自身反应性CD8(+) T细胞也可以下调自身免疫反应。最近的重要进展包括对某些自身免疫反应中导致自身反应性CD8(+) T细胞激活和募集的事件的机制理解,以及对这些T细胞在自身免疫中所起的多种作用有了更深入的认识。

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