Faculty of Medicine and Health Technology, Tampere University, Arvo Ylpön katu 34, 33520, Tampere, Finland.
Fimlab Laboratories, 33520, Tampere, Finland.
BioDrugs. 2019 Feb;33(1):15-32. doi: 10.1007/s40259-019-00333-w.
Cytokines, many of which signal through the JAK-STAT (Janus kinase-Signal Transducers and Activators of Transcription) pathway, play a central role in the pathogenesis of inflammatory and autoimmune diseases. Currently three JAK inhibitors have been approved for clinical use in USA and/or Europe: tofacitinib for rheumatoid arthritis, psoriatic arthritis and ulcerative colitis, baricitinib for rheumatoid arthritis, and ruxolitinib for myeloproliferative neoplasms. The clinical JAK inhibitors target multiple JAKs at high potency and current research has focused on more selective JAK inhibitors, almost a dozen of which currently are being evaluated in clinical trials. In this narrative review, we summarize the status of the pan-JAK and selective JAK inhibitors approved or in clinical trials, and discuss the rationale for selective targeting of JAKs in inflammatory and autoimmune diseases.
细胞因子通过 JAK-STAT(Janus 激酶-信号转导和转录激活因子)通路发挥作用,在炎症性和自身免疫性疾病的发病机制中发挥核心作用。目前,已有三种 JAK 抑制剂在美国和/或欧洲获得临床批准:托法替尼用于类风湿关节炎、银屑病关节炎和溃疡性结肠炎,巴利昔替尼用于类风湿关节炎,鲁索利替尼用于骨髓增生性肿瘤。临床 JAK 抑制剂以高活性针对多种 JAK,目前的研究集中在更具选择性的 JAK 抑制剂上,目前有十几个正在临床试验中进行评估。在本综述中,我们总结了已批准或正在临床试验中的泛 JAK 和选择性 JAK 抑制剂的状况,并讨论了在炎症性和自身免疫性疾病中选择性靶向 JAK 的原理。