JAK抑制剂:类风湿关节炎的新疗法

S. Jha
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引用次数: 0

摘要

在类风湿关节炎中,已经出现了从控制症状到通过消除炎症来控制疾病进展的范式转变。随着美国FDA于2012年11月批准首个JAK抑制剂Tofacitinib(未在欧洲),实现这种缓解或非常低的疾病活动性变得越来越可能。与TNFα抑制剂相比,这种新的小分子JAK抑制剂是一种作用于细胞内的口服药物,作用于细胞外空间的单一细胞因子,限制其自身于细胞表面受体。第二种JAK抑制剂Baracitinib于2017年2月在欧洲和2018年5月在美国获得批准,前景更大。成人中度至重度活动性类风湿关节炎患者,即使对一种或多种DMARDs / bDMARDs反应不充分或不耐受,每日口服一次2mg单药或与甲氨蝶呤联合使用也可获得缓解。它是甲氨蝶呤之后的安全二线治疗。在DMARD naïve患者中,它很可能成为一线药物
本文章由计算机程序翻译,如有差异,请以英文原文为准。
JAK inhibitors: Evolving therapies in rheumatoid arthritis
In rheumatoid arthritis, there has been a paradigm shift from controlling symptoms to controlling the disease progress with abrogation of inflammation. Achieving this remission or very low disease activity has become increasingly possible with USA FDA approved first JAK inhibitor, Tofacitinib in November 2012 (not in Europe). This new small molecule JAK inhibitors are oral drug working intra-cellularly in comparison to TNFα inhibitors targeting a singly cytokine within extra-cellular space confining themselves to cell surface receptors. The second JAK inhibitor Baracitinib approved in Europe in February 2017 and in USA in May 2018 has greater promises. Once daily 2 mg oral dose used either as monotherapy or in combination with methotrexate in moderate to severe active rheumatoid arthritis in adults have provided remission, even in patients who have responded inadequately or are intolerant to one or more DMARDs / bDMARDs. It is a safe second line therapy after methotrexate. In DMARD naïve patients, it is likely to become first-line agents
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