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针对中重度银屑病的新型生物制剂靶向白细胞介素-23 和白细胞介素-17。

Novel Biologic Agents Targeting Interleukin-23 and Interleukin-17 for Moderate-to-Severe Psoriasis.

机构信息

Department of Dermatology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, No. 301, Middle Yanchang Road, Jing'an District, Shanghai, 200072, China.

出版信息

Clin Drug Investig. 2017 Oct;37(10):891-899. doi: 10.1007/s40261-017-0550-z.

Abstract

Psoriasis is a common, chronic inflammatory skin disease and cannot be cured. The treatment of moderate-to-severe plaque psoriasis has been revolutionized with the development of biologic agents for nearly 20 years. Current studies show that interleukin-23 and interleukin-17 play remarkable roles in the pathogenesis of psoriasis. Interleukin-23 can sustain the differentiation and maintenance of T helper-17 lineage. Interleukin-17 can recruit and stimulate many cells, which play important parts in psoriasis through interacting with the interleukin-17 receptor. Several biologic agents targeting interleukin-23, interleukin-17, or their receptors are now in different stages: some are approved or clinical trials are in progress. Ustekinumab targets interleukin-23/interleukin-12p40; risankizumab, guselkumab, and tildrakizumab target interleukin-23p19; secukinumab and ixekizumab target interleukin-17A; and brodalumab targets the interleukin-17 receptors. All of these agents have good efficacy in treating moderate-to-severe psoriasis.

摘要

银屑病是一种常见的慢性炎症性皮肤病,无法治愈。近 20 年来,生物制剂的发展彻底改变了中重度斑块型银屑病的治疗方法。目前的研究表明,白细胞介素-23 和白细胞介素-17 在银屑病的发病机制中起着显著的作用。白细胞介素-23 可以维持辅助性 T 细胞 17 谱系的分化和维持。白细胞介素-17 可以通过与白细胞介素-17 受体相互作用招募和刺激许多在银屑病中起重要作用的细胞。目前有几种针对白细胞介素-23、白细胞介素-17 或其受体的生物制剂处于不同的阶段:有些已获得批准,有些正在进行临床试验。乌司奴单抗针对白细胞介素-23/白细胞介素-12p40;里司库单抗、古塞库单抗和替度鲁单抗针对白细胞介素-23p19;司库珠单抗和依奇珠单抗针对白细胞介素-17A;布罗达单抗针对白细胞介素-17 受体。所有这些药物在治疗中重度银屑病方面都有很好的疗效。

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