National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland.
University of Texas Southwestern Medical Center.
Arthritis Rheumatol. 2021 Dec;73(12):2166-2178. doi: 10.1002/art.41906. Epub 2021 Nov 2.
The discovery of cytokines and their role in immune and inflammatory disease led to the development of a plethora of targeted biologic therapies. Later, efforts to understand mechanisms of cytokine signal transduction led to the discovery of JAKs, which themselves were quickly identified as therapeutic targets. It has been a decade since the first JAK inhibitors (jakinibs) were approved, and there are now 9 jakinibs approved for the treatment of rheumatic, dermatologic, hematologic, and gastrointestinal indications, along with emergency authorization for COVID-19. In this review, we will summarize relevant discoveries that led to first-generation jakinibs and review their efficacy and safety as demonstrated in pivotal clinical studies. We will discuss the next generation of more selective jakinibs, along with agents that target kinase families beyond JAKs. Finally, we will reflect on both the opportunities and challenges ahead as we enter the second decade of the clinical use of jakinibs.
细胞因子的发现及其在免疫和炎症性疾病中的作用导致了大量靶向生物疗法的发展。后来,为了深入了解细胞因子信号转导的机制,人们发现了 JAKs,它们很快被确定为治疗靶点。自第一批 JAK 抑制剂(Jakinibs)获得批准以来已经过去了十年,现在已有 9 种 Jakinibs 获批用于治疗风湿、皮肤、血液和胃肠道疾病,并且针对 COVID-19 也获得了紧急授权。在这篇综述中,我们将总结导致第一代 Jakinibs 的相关发现,并回顾其在关键临床研究中表现出的疗效和安全性。我们将讨论下一代更具选择性的 Jakinibs,以及针对 JAK 以外激酶家族的药物。最后,我们将反思随着 Jakinibs 进入临床应用的第二个十年,未来所面临的机遇和挑战。