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依法利珠单抗停药:一种实用策略。

Efalizumab discontinuation: a practical strategy.

作者信息

Pugashetti Rupa, Koo John

机构信息

Department of Dermatology, University of California, San Francisco, CA 94118, USA.

出版信息

J Dermatolog Treat. 2009;20(3):132-6. doi: 10.1080/09546630902984596.

Abstract

Efalizumab is a recombinant, humanized IgG1 monoclonal antibody used in the treatment of plaque psoriasis. Efalizumab specifically targets T cells, leading to the subsequent inhibition of T-cell activation. The recent cases (three confirmed and one unconfirmed but suspected case) of the demyelinating disease progressive multifocal leukoencephalopathy (PML) have resulted in efalizumab being pulled from the market by European and Canadian regulatory agencies. Furthermore, manufacturer Genentech, Inc. has voluntarily withdrawn efalizumab from the United States market as of April 2009. In light of these events, this report is a practical guide to transitioning patients from efalizumab to alternative psoriasis therapies. The major consideration is the possibility for efalizumab-associated rebound of psoriasis. According to limited available literature and in the experience of the authors, the most effective agent for minimizing or preventing rebound is cyclosporine at the maximum dermatologic dose of 5 mg/kg per day.

摘要

依法利珠单抗是一种重组人源化IgG1单克隆抗体,用于治疗斑块状银屑病。依法利珠单抗特异性靶向T细胞,从而抑制T细胞的激活。近期出现的脱髓鞘疾病进行性多灶性白质脑病(PML)病例(3例确诊,1例未经证实但疑似)导致依法利珠单抗被欧洲和加拿大监管机构撤出市场。此外,制造商基因泰克公司已于2009年4月自愿从美国市场撤回依法利珠单抗。鉴于这些事件,本报告是一份指导患者从依法利珠单抗过渡到其他银屑病治疗方法的实用指南。主要考虑因素是依法利珠单抗相关的银屑病反弹可能性。根据有限的现有文献以及作者的经验,将银屑病反弹降至最低或预防其发生的最有效药物是环孢素,最大皮肤科剂量为每日5mg/kg。

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