Infectious Diseases Research Center, student research committee, Faculty of Medicine, Gonabad University of Medical Sciences, Gonabad, Iran.
Clinical Research Development Unit, Bohlool Hospital, Gonabad University of Medical Sciences, Gonabad, Iran.
J Dermatolog Treat. 2022 Dec;33(8):3098-3103. doi: 10.1080/09546634.2022.2116926. Epub 2022 Aug 29.
Lichen planus (LP) is an auto-inflammatory skin disorder identified by a presence of T-cell lymphocytes at the dermal-epidermal junction. It is hypothesized that the INF-γ/CXCL10 axis fulfills a major role in the onset and persistence of chronic inflammation in LP. Since Janus kinases (JAKs) are involved in the transduction of INF-γ signals, they may be good targets for LP treatment. Several case reports and case series described the safety and efficacy of upadacitinib (2 articles), tofacitinib (6 articles), baricitinib (4 articles), and Ruxolitinib (1 Article) in the treatment of LP variants. The predominant variants that JAK inhibitors improved were lichen planopilaris, nail LP, and erosive LP. Considering the role of the JAK pathway in LP pathogenesis and the evidence provided by these reports, it seems JAK inhibitors would be effective therapeutic agents for LP treatment. Hence, these agents should be trialed and evaluated further.
扁平苔藓(LP)是一种自身炎症性皮肤病,其特征是在真皮-表皮交界处存在 T 细胞淋巴细胞。据推测,IFN-γ/CXCL10 轴在 LP 的慢性炎症的发生和持续中起主要作用。由于 Janus 激酶(JAK)参与 INF-γ信号的转导,它们可能是 LP 治疗的良好靶点。有几篇病例报告和病例系列描述了乌帕替尼(2 篇文章)、托法替尼(6 篇文章)、巴瑞替尼(4 篇文章)和芦可替尼(1 篇文章)在 LP 变异型治疗中的安全性和有效性。JAK 抑制剂改善的主要变异型是扁平苔藓性脱发、甲扁平苔藓和糜烂性扁平苔藓。鉴于 JAK 通路在 LP 发病机制中的作用以及这些报告提供的证据,JAK 抑制剂似乎是 LP 治疗的有效治疗药物。因此,应该进一步试用和评估这些药物。