遗传增强
视网膜
医学
生物信息学
重症监护医学
基因
风险分析(工程)
生物
遗传学
眼科
作者
Pedro Antas,Cláudia Carvalho,Joaquim Cabral-Teixeira,Luísa de Lemos,Miguel C. Seabra
标识
DOI:10.1016/j.molmed.2023.11.009
摘要
Inherited retinal diseases (IRDs) stem from genetic mutations that result in vision impairment. Gene therapy shows promising therapeutic potential, exemplified by the encouraging initial results with voretigene neparvovec. Nevertheless, the associated costs impede widespread access, particularly in low-to-middle income countries. The primary challenge remains: how can we make these therapies globally affordable? Leveraging advancements in mRNA therapies might offer a more economically viable alternative. Furthermore, transitioning to nonviral delivery systems could provide a dual benefit of reduced costs and increased scalability. Relevant stakeholders must collaboratively devise and implement a research agenda to realize the potential of mRNA strategies in equitable access to treatments to prevent vision loss.
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