Janus激酶抑制剂治疗特应性皮炎。

Allergologie Select Pub Date : 2021-08-27 eCollection Date: 2021-01-01 DOI:10.5414/ALX02272E
Stephan Traidl, Sina Freimooser, Thomas Werfel
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引用次数: 33

摘要

在特应性皮炎(AD)中,JAK-STAT通路参与多种细胞因子驱动皮肤炎症的信号传导。Janus激酶(JAK)抑制剂靶向个体受体相关激酶,从而阻止炎症信号的介导。几种具有不同作用机制、效力和安全性的JAK抑制剂在局部和全身应用中都代表了AD的潜在治疗选择。JAK1/2选择性JAK抑制剂baricitinib是EMA批准用于全身口服治疗AD的首个此类药物。JAK1选择性抑制剂upadacitinib和abrocitinib的临床开发计划最终确定,对AD有阳性结果。PAN-JAK抑制剂delgocitinib是首个被批准用于治疗AD的药物(在日本)。这篇综述文章涵盖了越来越多的研究和批准的JAK抑制剂在治疗AD方面的数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Janus kinase inhibitors for the therapy of atopic dermatitis.

Janus kinase inhibitors for the therapy of atopic dermatitis.

The JAK-STAT pathway is involved in the signaling of multiple cytokines driving cutaneous inflammation in atopic dermatitis (AD). Janus kinase (JAK) inhibitors target individual receptor-associated kinases, thereby preventing the mediation of inflammatory signals. Several JAK inhibitors with varying mechanism of action, potency, and safety represent potential therapeutic options for AD in both topical and systemic application. The JAK1/2 selective JAK inhibitor baricitinib was the first substance from this class of drugs approved by the EMA for the systemic oral treatment of AD. The clinical development program of the JAK1 selective inhibitors upadacitinib and abrocitinib is finalized with positive results for AD. The PAN-JAK inhibitor delgocitinib was the first substance being approved for the treatment of AD (in Japan). This review article covers the rising data on investigational and approved JAK inhibitors in the context of the treatment of AD.

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