Recent progress in tyrosine kinase 2 inhibitors for atopic dermatitis.

IF 4.9 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Qi Liu, Yuan Xia, Lin Liu, Yuan Zhou, Yumei Li
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引用次数: 0

Abstract

Introduction: Atopic dermatitis (AD) is a chronic inflammatory skin disease characterized by persistent itching. Conventional treatments for AD include topical corticosteroids and calcineurin inhibitors, but there are emerging therapies targeting the JAK-TYK2 pathway that are promising for the treatment of AD.

Areas covered: This review comprehensively explores the pathogenesis, triggers, clinical manifestations, and conventional treatment options for AD. In addition, we discuss novel therapeutic agents targeting alternative signaling pathways, with a focus on clinical trials evaluating tyrosine kinase 2 (TYK2) inhibitors, including systemic and topical agents. We also provide a detailed assessment of ICP-332 efficacy, safety, and potential adverse effects in moderate-to-severe AD.

Expert opinion: Janus kinase inhibitors that have been recently approved have shown promise for the treatment of AD, especially for patients with severe phenotypes. Preliminary findings from randomized controlled trials suggest that TYK2 inhibitors exhibit rapid efficacy and acceptable safety in the management of AD; however, additional investigations, including long-term trials, are warranted to fully understand their efficacy and safety profile.

酪氨酸激酶 2 抑制剂治疗特应性皮炎的最新进展。
简介特应性皮炎(AD)是一种以持续瘙痒为特征的慢性炎症性皮肤病。特应性皮炎的传统治疗方法包括外用皮质类固醇激素和钙调磷酸酶抑制剂,但针对 JAK-TYK2 通路的新兴疗法在治疗特应性皮炎方面大有可为:本综述全面探讨了AD的发病机制、诱因、临床表现和常规治疗方案。此外,我们还讨论了针对替代信号通路的新型治疗药物,重点是评估酪氨酸激酶 2 (TYK2) 抑制剂(包括全身用药和局部用药)的临床试验。我们还对 ICP-332 在中重度 AD 中的疗效、安全性和潜在不良反应进行了详细评估:最近获批的 Janus 激酶抑制剂有望用于治疗 AD,尤其是表型严重的患者。随机对照试验的初步研究结果表明,TYK2抑制剂在治疗AD方面具有快速疗效和可接受的安全性;然而,要全面了解其疗效和安全性,还需要进行更多的研究,包括长期试验。
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来源期刊
CiteScore
10.00
自引率
0.00%
发文量
71
审稿时长
6-12 weeks
期刊介绍: Expert Opinion on Investigational Drugs (ISSN 1354-3784 [print], 1744-7658 [electronic]) is a MEDLINE-indexed, peer-reviewed, international journal publishing review articles and original papers on drugs in preclinical and early stage clinical development, providing expert opinion on the scope for future development. The Editors welcome: Reviews covering preclinical through to Phase II data on drugs or drug classes for specific indications, and their potential impact on future treatment strategies Drug Evaluations reviewing the clinical and pharmacological data on a particular drug Original Research papers reporting the results of clinical investigations on agents that are in Phase I and II clinical trials The audience consists of scientists, managers and decision-makers in the pharmaceutical industry, and others closely involved in R&D.
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