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JAK抑制剂:炎症性肠病口服疗法的新曙光。

JAK inhibitors: A new dawn for oral therapies in inflammatory bowel diseases.

作者信息

Herrera-deGuise Claudia, Serra-Ruiz Xavier, Lastiri Ernesto, Borruel Natalia

机构信息

Unitat d'Atenció Crohn-Colitis, Digestive System Research Unit, Hospital Universitari Vall d'Hebrón, Barcelona, Spain.

出版信息

Front Med (Lausanne). 2023 Mar 2;10:1089099. doi: 10.3389/fmed.2023.1089099. eCollection 2023.

Abstract

Inflammatory bowel disease (IBD) is a chronic immune-mediated condition of the gastrointestinal tract that requires chronic treatment and strict surveillance. Development of new monoclonal antibodies targeting one or a few single cytokines, including anti-tumor necrosis factor agents, anti-IL 12/23 inhibitors, and anti-α4β7 integrin inhibitors, have dominated the pharmacological armamentarium in IBD in the last 20 years. Still, many patients experience incomplete or loss of response or develop serious adverse events and drug discontinuation. Janus kinase (JAK) is key to modulating the signal transduction pathway of several proinflammatory cytokines directly involved in gastrointestinal inflammation and, thus, probably IBD pathogenesis. Targeting the JAK-STAT pathway offers excellent potential for the treatment of IBD. The European Medical Agency has approved three JAK inhibitors for treating adults with moderate to severe Ulcerative Colitis when other treatments, including biological agents, have failed or no longer work or if the patient cannot take them. Although there are currently no approved JAK inhibitors for Crohn's disease, upadacitinib and filgotinib have shown increased remission rates in these patients. Other JAK inhibitors, including gut-selective molecules, are currently being studied IBD. This review will discuss the JAK-STAT pathway, its implication in the pathogenesis of IBD, and the most recent evidence from clinical trials regarding the use of JAK inhibitors and their safety in IBD patients.

摘要

炎症性肠病(IBD)是一种慢性免疫介导的胃肠道疾病,需要长期治疗和严格监测。在过去20年中,针对一种或几种单一细胞因子的新型单克隆抗体的开发,包括抗肿瘤坏死因子药物、抗IL 12/23抑制剂和抗α4β7整合素抑制剂,在IBD的药物治疗中占据了主导地位。然而,许多患者仍经历反应不完全或丧失,或出现严重不良事件并停药。Janus激酶(JAK)是调节几种直接参与胃肠道炎症以及可能参与IBD发病机制的促炎细胞因子信号转导途径的关键。靶向JAK-STAT途径为IBD的治疗提供了巨大潜力。欧洲药品管理局已批准三种JAK抑制剂,用于治疗中度至重度溃疡性结肠炎的成人患者,前提是包括生物制剂在内的其他治疗方法已经失败、不再有效或患者无法使用。虽然目前尚无获批用于克罗恩病的JAK抑制剂,但乌帕替尼和非戈替尼已在这些患者中显示出缓解率提高。其他JAK抑制剂,包括肠道选择性分子,目前正在IBD中进行研究。本综述将讨论JAK-STAT途径、其在IBD发病机制中的作用,以及关于JAK抑制剂在IBD患者中的使用及其安全性的最新临床试验证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a788/10017532/0fdfd864d6ea/fmed-10-1089099-g001.jpg

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