tildrakizumab-asmn治疗中重度斑块型银屑病的概况:迄今为止的证据。

IF 5.2 Q1 DERMATOLOGY Psoriasis (Auckland, N.Z.) Pub Date : 2018-08-29 eCollection Date: 2018-01-01 DOI:10.2147/PTT.S146640
Kristen M Beck, Isabelle M Sanchez, Eric J Yang, Wilson Liao
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引用次数: 13

摘要

斑块型牛皮癣是一种免疫介导的皮肤病,在美国大约有3%的成年人患有此病。在过去的20年里,对银屑病免疫介导的病理生理学的研究取得了进展,这导致了针对银屑病的靶向生物疗法的发展。目前,被批准用于治疗斑块型银屑病的生物药物包括肿瘤坏死因子α抑制剂、白细胞介素(IL)-17或IL-17受体抑制剂、IL-12/23抑制剂和IL-23抑制剂。Tildrakizumab-asmn是一种靶向IL-23 p19亚基的单克隆抗体,已被批准用于中度至重度斑块性银屑病的成人患者,这些患者是全身治疗或光疗的候选人。本文综述了目前tildrakizumab-asmn的药理学、疗效和安全性数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Profile of tildrakizumab-asmn in the treatment of moderate-to-severe plaque psoriasis: evidence to date.

Plaque psoriasis is an immune-mediated skin disease that affects roughly 3% of adults in the United States. Advances over the past 20 years in understanding the immune-mediated pathophysiology of psoriasis have led to the development of targeted biologic therapies for this condition. Currently, biologic medications approved for the treatment of plaque psoriasis include tumor necrosis factor α inhibitors, interleukin (IL)-17 or IL-17 receptor inhibitors, IL-12/23 inhibitors, and IL-23 inhibitors. Tildrakizumab-asmn is a monoclonal antibody that targets the p19 subunit of IL-23 and is approved for use in adult patients with moderate-to-severe plaque psoriasis who are candidates for systemic therapy or phototherapy. This article reviews the current pharmacologic, efficacy, and safety data on tildrakizumab-asmn.

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