1 SKiN Centre for Dermatology, Peterborough, ON, Canada.
2 Trent University, Peterborough, ON, Canada.
J Cutan Med Surg. 2019 May/Jun;23(3):289-297. doi: 10.1177/1203475418824079. Epub 2019 Jan 28.
Alopecia areata (AA) is a chronic, immune-mediated disorder that targets hair follicle epithelium, thereby restricting hair growth in localized patches. Although several therapies for AA have been tested, responses with traditional therapies have been limited. In recent years, numerous reports have been published of patients with AA responding to Janus kinase (JAK) inhibitors. This literature review aims to describe AA pathophysiology, explore how and why JAK inhibitors can be used for AA treatment, and review published case reports, case series, and open-label studies published to date. Pathogenesis of AA includes interactions between genetic, environmental, and immune factors and is mediated by the cytokines interferon-γ and interleukin (IL)-15. JAK inhibition resulting in hair regrowth in some cases supports that AA is associated with the Janus kinase-signal transducer and activator of transcription (JAK-STAT) signaling pathway. The emergence of JAK inhibitors for AA therapy is changing the way health care providers think about and treat AA. A mixture of animal model studies and human case studies have reported the use of baricitinib (JAK 1/2), ruxolitinib (JAK 1/2), and tofacitinib (JAK 1/3) for the management of AA. JAK inhibition has shown potential as an effective AA therapy when used in case studies, case series, and open-label trials. Formal clinical trials are ongoing and will yield more definitive conclusions about the safety and efficacy of JAK inhibitors.
斑秃(AA)是一种慢性、免疫介导的疾病,靶向毛囊上皮,从而限制局部斑块的毛发生长。尽管已经测试了几种 AA 的治疗方法,但传统疗法的反应有限。近年来,有大量关于 AA 患者对 Janus 激酶(JAK)抑制剂有反应的报告。本文献综述旨在描述 AA 的发病机制,探讨 JAK 抑制剂如何以及为何可用于 AA 的治疗,并回顾迄今为止发表的病例报告、病例系列和开放标签研究。AA 的发病机制包括遗传、环境和免疫因素之间的相互作用,由干扰素-γ和白细胞介素(IL)-15 介导。JAK 抑制导致一些情况下的毛发再生支持 AA 与 Janus 激酶-信号转导和转录激活因子(JAK-STAT)信号通路有关。JAK 抑制剂用于 AA 治疗的出现正在改变医疗保健提供者对 AA 的治疗思路。动物模型研究和人类病例研究的混合报告了巴瑞替尼(JAK1/2)、芦可替尼(JAK1/2)和托法替尼(JAK1/3)用于 AA 的管理。在病例研究、病例系列和开放标签试验中,JAK 抑制已显示出作为一种有效的 AA 治疗方法的潜力。正在进行正式的临床试验,将得出关于 JAK 抑制剂的安全性和有效性的更明确结论。