Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Department of Medicine, Queen's University, Kingston, Ontario, Canada.
Int J Dermatol. 2022 Feb;61(2):139-147. doi: 10.1111/ijd.15605. Epub 2021 Apr 30.
Increasing understanding of cytokines as major drivers of immune-mediated diseases has revolutionized targeted treatments for these conditions. As the pathogenesis of autoimmune conditions is mediated by a complex interplay of various cytokines, Janus kinase (JAK) inhibitors have been of particular interest due to their ability to target multiple cytokines simultaneously. However, due to safety concerns with first generation JAK inhibitors, most notably from JAK2 and JAK3 inhibition, interest has shifted to more selective inhibition of TYK2. Three key TYK2 inhibitors that have advanced furthest in clinical trials for treatment of dermatologic autoimmune conditions are deucravacitinib (BMS-986165), brepocitinib (PF-06700841), and PF-06826647. This review outlines the current understanding of the efficacy and safety of these three TYK2 inhibitors from completed phase I and II studies and summarizes studies currently in progress for dermatologic conditions.
随着人们对细胞因子作为免疫介导性疾病主要驱动因子的认识不断加深,针对这些疾病的靶向治疗也取得了革命性进展。由于自身免疫性疾病的发病机制是由多种细胞因子的复杂相互作用介导的,因此 Janus 激酶(JAK)抑制剂因其能够同时靶向多种细胞因子而备受关注。然而,由于第一代 JAK 抑制剂(尤其是 JAK2 和 JAK3 抑制剂)存在安全性问题,人们的兴趣已转向对 TYK2 的更选择性抑制。在治疗皮肤科自身免疫性疾病的临床试验中,有三种处于领先地位的关键 TYK2 抑制剂,分别是德瓦鲁单抗(BMS-986165)、布罗昔替尼(PF-06700841)和 PF-06826647。这篇综述概述了这三种 TYK2 抑制剂在已完成的 I 期和 II 期研究中的疗效和安全性的现有认识,并总结了目前正在进行的针对皮肤科疾病的研究。