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肿瘤坏死因子相关凋亡诱导配体(TRAIL)在类风湿关节炎中的作用:有哪些新进展?

TNF-related apoptosis-inducing ligand (TRAIL) in rheumatoid arthritis: what's new?

机构信息

Department of Medical and Surgical Sciences, Rheumatology Clinic, University of Foggia, Ospedale "Col. D'Avanzo", V.le degli Aviatori 1, 71100, Foggia, Italy.

出版信息

Clin Exp Med. 2014 May;14(2):115-20. doi: 10.1007/s10238-012-0226-1. Epub 2012 Dec 30.

Abstract

TNF-related apoptosis-inducing ligand (TRAIL) is a type II transmembrane protein of the TNF superfamily that serves as an extracellular signal that triggers programmed cell death in tumor cells, without affecting normal cells. Recently, scientists have turned their attention to the emerging role of TRAIL in immune and autoimmune responses. TRAIL has been shown to down-regulate the self-antigens in autoimmune diseases, such as rheumatoid arthritis (RA) by exerting its apoptotic effect on activated T cells and synoviocytes and by its local anti-inflammatory effect. The impact of TRAIL molecular variants and agonistic monoclonal antibodies in the regulation of TRAIL activity in arthritis animal models strongly supports the idea of testing the role of TRAIL in humans, with the aim of developing new effective therapies that promote apoptosis of synoviocytes and/or infiltrating lymphocytes, by targeting TRAIL. The aim of this review is to summarize recent progress and current knowledge of TRAIL functions in RA.

摘要

肿瘤坏死因子相关凋亡诱导配体(TRAIL)是肿瘤坏死因子超家族的一种 II 型跨膜蛋白,作为一种细胞外信号,在不影响正常细胞的情况下,触发肿瘤细胞的程序性细胞死亡。最近,科学家们将注意力转向 TRAIL 在免疫和自身免疫反应中的新作用。TRAIL 通过对活化的 T 细胞和滑膜细胞发挥其凋亡作用,并通过其局部抗炎作用,已被证明可下调类风湿关节炎(RA)等自身免疫性疾病中的自身抗原。TRAIL 分子变异体和激动性单克隆抗体在关节炎动物模型中调节 TRAIL 活性的影响强烈支持在人类中测试 TRAIL 作用的想法,目的是开发新的有效疗法,通过靶向 TRAIL 促进滑膜细胞和/或浸润淋巴细胞的凋亡。本综述的目的是总结 TRAIL 在 RA 中的作用的最新进展和现有知识。

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