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风湿性疾病中 JAK/STAT 信号通路的抑制:不断扩大的研究范围。

Inhibition of JAK/STAT signaling in rheumatologic disorders: The expanding spectrum.

机构信息

Department of Internal Medicine, Lyon University Hospital, 69004 Lyon, France.

Department of Internal Medicine, Lyon University Hospital, 69004 Lyon, France.

出版信息

Joint Bone Spine. 2020 Mar;87(2):119-129. doi: 10.1016/j.jbspin.2019.09.005. Epub 2019 Sep 12.

Abstract

Three Janus kinase (JAK) inhibitors, ruxolitinib, tofacitinib, and baricitinib, are currently approved by the FDA/EMA for the treatment of rheumatoid arthritis, psoriatic arthritis, and ulcerative rectocolitis. The inhibition of JAK/STAT signaling by these small molecules, downstream of several cytokine receptors, results in lower pro-inflammatory gene expression. Given the cytokine profiles observed in rheumatologic diseases, most of the recent therapeutic strategies target cytokines, either directly or through their receptors. Each cytokine receptor recruits a specific combination of JAKs to activate different programs in cells. The approved drugs are panJAK inhibitors, able to impede more than one pathway. These drugs are being tested in various rheumatologic disorders. At the same time, more specific molecules able to target one specific JAK are being developed. In this review, we describe the expanding spectrum of rheumatologic and autoimmune conditions for which JAK inhibition may represent new avenues in clinical practice.

摘要

三种 Janus 激酶(JAK)抑制剂,鲁索利替尼、托法替尼和巴瑞替尼,目前已被 FDA/EMA 批准用于治疗类风湿关节炎、银屑病关节炎和溃疡性结肠炎。这些小分子通过细胞因子受体下游的 JAK/STAT 信号通路抑制,导致促炎基因表达降低。鉴于风湿性疾病中观察到的细胞因子谱,大多数最近的治疗策略针对细胞因子,无论是直接靶向还是通过其受体靶向。每种细胞因子受体招募特定的 JAK 组合,在细胞中激活不同的程序。已批准的药物是泛 JAK 抑制剂,能够抑制多种途径。这些药物正在各种风湿性疾病中进行测试。与此同时,正在开发能够针对特定 JAK 的更特异的分子。在这篇综述中,我们描述了 JAK 抑制可能代表临床实践中开辟新途径的不断扩大的风湿和自身免疫性疾病谱。

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