黄斑变性
遗传增强
医学
变性(医学)
基因
眼科
生物
遗传学
作者
Normila Barthelemy,Jayanth Sridhar,Jesse D. Sengillo
出处
期刊:Bioengineering
[Multidisciplinary Digital Publishing Institute]
日期:2025-10-02
卷期号:12 (10): 1072-1072
标识
DOI:10.3390/bioengineering12101072
摘要
The prevalence of wet age-related macular degeneration (AMD) in the US is expected to increase to 82 million by 2050. Addressing the specialized needs for this population will become increasingly challenging as prevalence rises. Frequent anti-vascular endothelial growth factor (anti-VEGF) injections have been the recourse for this population; however, the burden wet AMD places on patients underscores the critical need for durable therapeutic approaches. Gene therapy is a bioengineered treatment that has transformed the management of previously untreatable disorders. Ongoing advancements and refinements in its biomechanism could lead to more sustainable treatment options for wet AMD. In this article, we provide recent updates on gene therapy trials for wet AMD.
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