为干湿性老年性黄斑变性寻找更持久有效的治疗方法

A. Arrigo, F. Bandello
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引用次数: 0

摘要

在发达国家,年龄相关性黄斑变性(AMD)是导致视力丧失的主要原因。AMD的晚期特征是黄斑新生血管或地理萎缩的发生和发展。基于玻璃体内抗血管内皮生长因子(anti-VEGF)药物,目前有几种治疗方法可用于管理新血管形式的AMD。虽然这些药物在诱导体液退化和保持视觉功能方面是有效的,但它们有限的作用时间和治疗负担刺激了具有更持久药理活性的新分子的发展。未来的渗出性AMD治疗将包括新一代抗vegf药物、手术抗vegf港口递送系统和作用于其他AMD致病途径的新分子。相比之下,干性AMD和地理萎缩没有批准的治疗方法;营养方法仍然是减少AMD进展和并发症发生概率的唯一途径。几个正在进行的临床试验正在测试不同的分子,这些分子已经开发出来,可以减缓地理萎缩的进展,包括补体系统抑制剂、整合素抑制剂、基因疗法和细胞疗法。在这篇综述中,我们概述了干湿性AMD的治疗现状和未来的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Towards the Development of Longer and More Efficacious Therapies for Wet and Dry Age-related Macular Degeneration
Age-related macular degeneration (AMD) is a leading cause of vision loss in developed countries. The advanced stages of AMD are characterized by the onset and progression of macular neovascularization or geographic atrophy. Several treatments are currently available for managing the neovascular form of AMD, based on intravitreal anti-vascular endothelial growth factor (anti-VEGF) drugs. Although these agents are efficient in inducing fluid regression and preserving visual function, their limited duration of action and treatment burden are stimulating the development of new molecules with more prolonged pharmacological activity. The future of exudative AMD therapies will include new generations of anti-VEGF drugs, surgical anti-VEGF port delivery systems and novel molecules acting on other AMD pathogenic pathways. In contrast, dry AMD and geographic atrophy have no approved treatments; nutraceutical approaches still represent the only way to reduce the probability of AMD progression and the onset of complications. Several ongoing clinical trials are testing different molecules that have been developed to slow the progression of geographic atrophy, including complement system inhibitors, integrin inhibitors, gene therapies and cell-based therapies. In this review, we provide an overview of the current state of the art and future perspectives for the management of dry and wet AMD.
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