Department of Gastroenterology, Herlev Hospital, University of Copenhagen, Copenhagen, Denmark.
Department of Gastroenterology, Herlev Hospital, University of Copenhagen, Copenhagen, Denmark.
Trends Pharmacol Sci. 2022 May;43(5):424-436. doi: 10.1016/j.tips.2022.02.008. Epub 2022 Mar 8.
Recent significant advances have been made in the treatment of chronic inflammatory diseases with initiation of the era of biologics. However, an unmet medical need still exists for novel targeted therapies. Compared with biologics, Janus kinase inhibitors (JAKis) are a new drug class of orally administered small molecules that have been shown to efficiently modulate complex cytokine-driven inflammation in preclinical models and human studies. Unfortunately, serious adverse effects have been reported with the first introduced pan-JAKi, tofacitinib. Here, we review tyrosine kinase 2 (TYK2) signaling in the pathophysiology of inflammatory bowel disease (IBD), examine mechanisms of action of selective TYK2 inhibitors (TYK2is), and discuss the potential for these inhibitors in efforts to balance benefits and harms.
近年来,生物制剂时代的到来使得慢性炎症性疾病的治疗取得了重大进展。然而,仍然存在新的靶向治疗的未满足的医学需求。与生物制剂相比,Janus 激酶抑制剂(JAKi)是一种新型的口服小分子药物类别,已在临床前模型和人类研究中证明可有效调节复杂的细胞因子驱动的炎症。不幸的是,首先引入的泛 JAKi,托法替尼,已报告了严重的不良反应。在这里,我们回顾了酪氨酸激酶 2(TYK2)在炎症性肠病(IBD)发病机制中的信号转导,研究了选择性 TYK2 抑制剂(TYK2i)的作用机制,并讨论了这些抑制剂在平衡获益和危害方面的潜力。