光遗传学
色素性视网膜炎
神经科学
医学
视网膜变性
视网膜植入物
视网膜
黄斑变性
临床试验
遗传增强
生物信息学
眼科
生物
病理
基因
遗传学
作者
Ehab Kasem,Masa Watfa,Ali Afif,Raghad Hasan,Majd Mansour,Haya Almhmoud,Basem Zaino
标识
DOI:10.1177/11206721251335560
摘要
Optogenetics, a cutting-edge tool in novel gene manipulation and drug discovery, holds significant therapeutic potential for a variety of neurological disorders, including retinal diseases. Retinal diseases such as age-related macular degeneration (AMD) and retinitis pigmentosa (RP), significantly impair quality of life and cause severe visual impairment due to limited treatment options and a general lack of awareness. The increasing incidence of these degenerative conditions underscores the need for innovative solutions, such as optogenetics. Optogenetic therapy introduces genes coding for light-sensitive proteins, which are controlled by light signals to make neurons photosensitive. This precise targeting approach does not require specific gene intervention and can bypass dysfunctional photoreceptors, offering a treatment option for various degenerative and dystrophic eye diseases. Successful outcomes in patients with late-stage genetic retinal diseases and numerous clinical trials suggest that optogenetics could be an effective treatment for humans. This review provides an overview of the current landscape of optogenetic therapy, discusses its challenges, and summarizes the findings of ongoing clinical trials for neural and visual restoration.
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