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JAK 抑制剂:在炎症性肠病治疗策略中的应用现状。

JAK inhibitors: current position in treatment strategies for use in inflammatory bowel disease.

机构信息

Division of Gastroenterology, Department of Medicine, University of Toronto, Toronto, Ontario, Canada; Department of Gastroenterology, Faculty of Medicine, Pontificia Universidad Católica of Chile, Santiago, Chile.

Division of Gastroenterology, Department of Medicine, University of California San Diego, La Jolla, CA, USA.

出版信息

Curr Opin Pharmacol. 2020 Dec;55:99-109. doi: 10.1016/j.coph.2020.10.010. Epub 2020 Nov 15.

Abstract

Our expanding knowledge of the pathophysiology of inflammatory bowel disease (IBD) has led to the development of a multitude of new therapies, including parenterally administrated biologic agents and new oral small molecules. Tofacitinib is the first compound of a promising class of new small molecules approved for the treatment of IBD. This pan-Janus kinase (JAK) inhibitor (JAKi) targets the four isoforms of cytokine associated JAKs (JAK1, JAK2, JAK3 and TYK2). Next generations JAKi with marked selectivity for specific JAK isoforms or gut-restricted effect are in development, with promising results in phase I and II clinical trials. Whether increased JAK selectivity will translate into more favorable clinical efficacy and safety profiles remains to be demonstrated in larger clinical trials. Here we provide an overview of the clinical and pharmacological aspects of these drugs and discuss how they may be incorporated in the current treatment paradigm for Crohn's disease and ulcerative colitis.

摘要

我们对炎症性肠病(IBD)病理生理学的认识不断扩大,导致了多种新疗法的发展,包括肠外给予的生物制剂和新型口服小分子药物。托法替布是一类有前途的新型小分子药物中的首个获批用于治疗 IBD 的化合物。这种泛 Janus 激酶(JAK)抑制剂(JAKi)针对与细胞因子相关的四种 JAK 同工型(JAK1、JAK2、JAK3 和 TYK2)。正在开发对特定 JAK 同工型具有显著选择性或肠道限制作用的下一代 JAKi,并在 I 期和 II 期临床试验中取得了有前景的结果。增加 JAK 选择性是否会转化为更有利的临床疗效和安全性仍有待更大规模临床试验证明。本文提供了这些药物的临床和药理学方面的概述,并讨论了它们如何可被纳入目前用于治疗克罗恩病和溃疡性结肠炎的治疗模式。

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