Liang Jingyao, Li Wei, Liu Wenyan, Yu Yihui, Ye Hui, Zhang Xibao
Institute of Dermatology, Guangzhou Medical University, Guangzhou, Guangdong, 510095, People's Republic of China.
Department of Dermatology, Guangzhou Dermatology Hospital, Guangzhou, Guangdong, 510095, People's Republic of China.
Clin Cosmet Investig Dermatol. 2024 Aug 6;17:1793-1797. doi: 10.2147/CCID.S470641. eCollection 2024.
Prurigo nodularis (PN) is a debilitating chronic neuroimmunologic skin condition due to the intense pruritus and difficult to treat. The pruritogenic cytokines, particularly IL-4, IL-13, IL-22, IL-31, and oncostatin M (OSM), play a crucial role in the pathogenesis of PN, potentially involving the JAK1-STAT pathway. An oral JAK1 inhibitor, abrocitinib, is presently undergoing Phase 2 trials for the treatment of PN. We evaluated the efficacy of abrocitinib at a daily dosage of 100 mg in treating two patients with PN affecting both lower limbs: a 50-year-old male with a 16-year disease history and a 38-year-old female with over three years of disease history, both of whom had failed to respond to multiple conventional treatments. Both patients responded rapidly after one week of treatment and exhibited a marked improvement. Following eight weeks of therapy, near-complete resolution of both pruritus and lesions was achieved, and no adverse effects were reported. Additionally, there were no reported side effects during the initial four months of continued treatment. Abrocitinib is an effective targeted therapy for PN, offering a promising new option for refractory patients.
结节性痒疹(PN)是一种使人衰弱的慢性神经免疫性皮肤病,因剧烈瘙痒且难以治疗。致痒细胞因子,特别是白细胞介素-4(IL-4)、白细胞介素-13(IL-13)、白细胞介素-22(IL-22)、白细胞介素-31(IL-31)和制瘤素M(OSM),在PN的发病机制中起关键作用,可能涉及JAK1-STAT途径。一种口服JAK1抑制剂阿布昔替尼目前正在进行治疗PN的2期试验。我们评估了每日剂量100 mg的阿布昔替尼对两名双下肢患有PN的患者的疗效:一名50岁男性,有16年病史;一名38岁女性,有三年多病史,两人对多种传统治疗均无反应。两名患者在治疗一周后迅速起效,症状明显改善。经过八周治疗,瘙痒和皮损几乎完全消退,且未报告有不良反应。此外,在持续治疗的最初四个月也未报告有副作用。阿布昔替尼是治疗PN的一种有效靶向疗法,为难治性患者提供了一种有前景的新选择。