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用于晚期干性年龄相关性黄斑变性(地图样萎缩)的补体抑制剂:隧道尽头有曙光了吗?

Complement Inhibitors for Advanced Dry Age-Related Macular Degeneration (Geographic Atrophy): Some Light at the End of the Tunnel?

作者信息

Cruz-Pimentel Miguel, Wu Lihteh

机构信息

Department of Ophthalmology and Vision Sciences, University of Toronto, Toronto, ON M5S 1A1, Canada.

Asociados de Macula, Vitreo y Retina de Costa Rica, Primer Piso Torre Mercedes Paseo Colon, San José 10102, Costa Rica.

出版信息

J Clin Med. 2023 Aug 4;12(15):5131. doi: 10.3390/jcm12155131.

Abstract

Geographic atrophy (GA) affects around 5 million individuals worldwide. Genome-wide, histopathologic, in vitro and animal studies have implicated the activation of the complement system and chronic local inflammation in the pathogenesis of GA. Recently, clinical trials have demonstrated that an intravitreal injection of pegcetacoplan, a C3 inhibitor, and avacincaptad pegol, a C5 inhibitor, both statistically significantly reduce the growth of GA up to 20% in a dose-dependent fashion. Furthermore, the protective effect of both pegcetacoplan and avacincaptad appear to increase with time. However, despite these anatomic outcomes, visual function has not improved as these drugs appear to only slow down the degenerative process. Unexpected adverse events included conversion to exudative NV-AMD with both drugs. Occlusive retinal vasculitis and anterior ischemic optic neuropathy have been reported in pegcetacoplan-treated eyes.

摘要

地图样萎缩(GA)在全球影响着约500万人。全基因组、组织病理学、体外及动物研究表明,补体系统激活和慢性局部炎症与GA的发病机制有关。最近,临床试验证明,玻璃体内注射C3抑制剂培西加可普朗和C5抑制剂阿伐西普,二者均能以剂量依赖方式使GA生长在统计学上显著降低达20%。此外,培西加可普朗和阿伐西普的保护作用似乎随时间增加。然而,尽管有这些解剖学结果,但由于这些药物似乎仅减缓了退行性过程,视觉功能并未改善。意外不良事件包括两种药物均导致转为渗出性新生血管性年龄相关性黄斑变性(NV-AMD)。培西加可普朗治疗的眼睛中曾报告有闭塞性视网膜血管炎和前部缺血性视神经病变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a27/10420150/f8510988cf03/jcm-12-05131-g001.jpg

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