J Clin Invest. 2018 Jul 2;128(7):2760-2762. doi: 10.1172/JCI121526. Epub 2018 Jun 11.
Interferonopathies are a subset of autoinflammatory disorders with a prominent type I IFN gene signature. Treatment of these patients has been challenging, given the lack of response to common autoinflammatory therapeutics including IL-1 and TNF blockade. JAK inhibitors (Jakinibs) are a family of small-molecule inhibitors that target the JAK/STAT signaling pathway and have shown clinical efficacy, with FDA and European Medicines Agency (EMA) approval for arthritic and myeloproliferative syndromes. Sanchez and colleagues repurposed baricitinib to establish a significant role for JAK inhibition as a novel therapy for patients with interferonopathies, demonstrating the power of translational rare disease research with lifesaving effects.
干扰素病是自身炎症性疾病的一个亚类,具有显著的 I 型 IFN 基因特征。由于对常见的自身炎症治疗方法(包括 IL-1 和 TNF 阻断)没有反应,这些患者的治疗一直具有挑战性。JAK 抑制剂(Jakinibs)是一类小分子抑制剂,靶向 JAK/STAT 信号通路,已显示出临床疗效,获得了美国食品和药物管理局(FDA)和欧洲药品管理局(EMA)批准,用于治疗关节炎和骨髓增生性综合征。Sanchez 及其同事重新利用巴瑞替尼来确定 JAK 抑制作为干扰素病患者的一种新型治疗方法的重要作用,展示了具有救生效果的转化性罕见病研究的力量。