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中枢神经系统自身免疫性疾病中 STAT 通路的治疗靶点

Therapeutic targeting of STAT pathways in CNS autoimmune diseases.

作者信息

Egwuagu Charles E, Larkin Iii Joseph

机构信息

Molecular Immunology Section; National Eye Institute; National Institutes of Health; Bethesda, MD USA.

出版信息

JAKSTAT. 2013 Jan 1;2(1):e24134. doi: 10.4161/jkst.24134.

Abstract

Signal transducers and activators of transcription (STATs) transduce extracellular signals that regulate the initiation, duration and intensity of immune responses. However, unbridled activation of STATs by pro-inflammatory cytokines or growth factors contributes to pathogenic autoimmunity. In this review, we briefly discuss STAT pathways that promote the development and expansion of T cells that mediate two CNS inflammatory diseases, multiple sclerosis (MS) and uveitis. Particular focus is on animal models of MS and uveitis and new approaches to the treatment of CNS autoimmune diseases based on therapeutic targeting of Th17 cells and STAT pathways.

摘要

信号转导及转录激活因子(STATs)可转导细胞外信号,这些信号调节免疫反应的起始、持续时间和强度。然而,促炎细胞因子或生长因子对STATs的无节制激活会导致致病性自身免疫。在本综述中,我们简要讨论促进介导两种中枢神经系统炎症性疾病——多发性硬化症(MS)和葡萄膜炎的T细胞发育和扩增的STAT途径。特别关注MS和葡萄膜炎的动物模型,以及基于对Th17细胞和STAT途径进行治疗性靶向的中枢神经系统自身免疫性疾病的新治疗方法。

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