贾纳斯激酶
托法替尼
医学
银屑病
鲁索利替尼
JAK-STAT信号通路
激酶
药理学
促炎细胞因子
Janus激酶抑制剂
癌症研究
酪氨酸激酶
免疫学
炎症
内科学
细胞因子
受体
生物
细胞生物学
类风湿性关节炎
骨髓
骨髓纤维化
作者
Sylwia Słuczanowska-Głąbowska,Anna Ziegler-Krawczyk,Kamila Szumilas,Andrzej Pawlik
摘要
Janus kinases inhibitors are molecules that target Janus kinases-signal transducers and activators of transcription (JAK/STAT). They inhibit this intracellular signal pathway, blocking the gene transcription of crucial proinflammatory cytokines that play a central role in the pathogenesis of many inflammatory and autoimmune diseases, including psoriasis. This process reduces psoriatic inflammation. The JAK inhibitors are divided into two generations. The first generation of JAK inhibitors blocks two or more different Janus kinases. The second generation is more specified and blocks only one type of Janus kinase and has less side effects than the first generation. Tofacitinib, ruxolitinib and baricitinib belong to first generation JAK inhibitors and decernotinib and filgotinib belong to second group. This narrative review summarizes the role of Janus kinase inhibitors in the therapy of psoriasis. Oral JAK inhibitors show promise for efficacy and safety in the treatment of psoriasis. Studies to date do not indicate that JAK inhibitors are superior to recent biologic drugs in terms of efficacy. However, JAK inhibitors, due to their lack of increased incidence of side effects compared to other biologic drugs, can be included in the psoriasis treatment algorithm because they are orally taken. Nevertheless, further studies are needed to evaluate long-term treatment effects with these drugs.
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