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银屑病的新型生物制剂:IL-23和IL-17抑制剂的最新进展

New biologics in psoriasis: an update on IL-23 and IL-17 inhibitors.

作者信息

Dong Joanna, Goldenberg Gary

机构信息

Department of Dermatology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.

出版信息

Cutis. 2017 Feb;99(2):123-127.

Abstract

As immune-related pathways involved in the pathogenesis of psoriasis are elucidated, new biologic treatments targeting these steps of the psoriatic immune cascade are developed. In this article, we review the literature on IL-23 and IL-17 inhibitors in the pipeline for use in moderate to severe psoriasis. Numerous pipeline biologic therapies, including risankizumab, guselkumab, tildrakizumab, ixekizumab, and brodalumab, are being investigated in phase 2 and 3 studies to establish the efficacy and safety of these new agents. Of these newest biologics being studied for psoriasis, ixekizumab has been approved and brodalumab is pending approval by the US Food and Drug Administration.

摘要

随着与银屑病发病机制相关的免疫途径得以阐明,针对银屑病免疫级联反应这些环节的新型生物疗法应运而生。在本文中,我们回顾了正在研发的用于治疗中重度银屑病的白细胞介素-23(IL-23)和白细胞介素-17(IL-17)抑制剂的相关文献。众多正在研发的生物疗法,包括瑞莎珠单抗、古塞库单抗、替拉珠单抗、依奇珠单抗和布罗达单抗,正在进行2期和3期研究,以确定这些新药的疗效和安全性。在这些用于治疗银屑病的最新生物制剂中,依奇珠单抗已获批准,布罗达单抗正待美国食品药品监督管理局批准。

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