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利用光遗传学恢复视力,而不会对风险视而不见。

Restoring vision using optogenetics without being blind to the risks.

机构信息

Aikenhead Centre for Medical Discovery, ARC Centre of Excellence for Electromaterials Science, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Melbourne, VIC, 3010, Australia.

School of Humanities, University of Tasmania, Hobart, Australia.

出版信息

Graefes Arch Clin Exp Ophthalmol. 2022 Jan;260(1):41-45. doi: 10.1007/s00417-021-05477-6. Epub 2021 Nov 1.

Abstract

Retinit is pigmentosa is an incurable degenerative disease that causes loss of light-sensitive cells in the retina and leads to severe vision impairment. The development of optogenetics has created great hype around its potential to treat retinitis pigmentosa by the introduction of light-sensitive proteins into other neural cells in the retina. The first-in-human studies of optogenetic treatment for this disease have recently been reported (NCT02556736 and NCT03326336). The treatment involves irreversible gene therapy and requires access to specially designed goggles to deliver light to the treated eye. These highly innovative and high-profile clinical trials raise numerous ethical issues that must be addressed during the early phases of research and clinical testing to ensure trial participants are treated fairly and can provide appropriate informed consent.

摘要

色素性视网膜炎是一种无法治愈的退行性疾病,它会导致视网膜中的感光细胞丧失,从而导致严重的视力障碍。光遗传学的发展引发了人们对其治疗色素性视网膜炎潜力的极大关注,即将感光蛋白引入视网膜中的其他神经细胞。最近已经报道了针对这种疾病的光遗传学治疗的首次人体研究(NCT02556736 和 NCT03326336)。该治疗涉及不可逆的基因疗法,并且需要使用专门设计的护目镜将光输送到治疗眼。这些极具创新性和备受瞩目的临床试验引发了许多伦理问题,在研究和临床测试的早期阶段必须解决这些问题,以确保试验参与者得到公平对待并能够提供适当的知情同意。

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