Department of Ophthalmology, Casey Eye Institute, Oregon Health & Science University, Portland, OR, USA.
Division of Neuroscience, Oregon National Primate Research Center, Oregon Health & Science University, Portland, OR, USA.
Adv Exp Med Biol. 2018;1074:641-647. doi: 10.1007/978-3-319-75402-4_78.
Transplantation of potentially therapeutic cells into the subretinal space is a promising prospective therapy for the treatment of retinal degenerative diseases including age-related macular degeneration (AMD). In rodent models with photoreceptor degeneration, subretinal transplantation of cell suspensions has repeatedly been demonstrated to rescue behaviorally measured vision, maintain electrophysiological responses from the retina and the brain, and slow the degeneration of rod and cone photoreceptors for extended periods. These studies have led to the initiation of a number of FDA-approved clinical trials for application of cell-based therapy for AMD and other retinal degenerative diseases. However, translation from rodent models directly into human clinical trials skips an important intermediary preclinical step that is needed to address critical issues for intraocular cell transplantation. These include determination of the most appropriate and least problematic surgical approach, the application of treatment in an eye with similar size and structure including the presence of a macula, and a thorough understanding of the immunological considerations regarding graft survival and the consequences of grafted cell rejection. This chapter will review these and related issues and will document current efforts to address these concerns.
将有治疗潜力的细胞移植到视网膜下腔是治疗包括年龄相关性黄斑变性(AMD)在内的视网膜退行性疾病的一种很有前途的治疗方法。在感光细胞变性的啮齿动物模型中,视网膜下移植细胞悬液已被反复证明可以挽救行为测量的视力,维持视网膜和大脑的电生理反应,并延长杆状和锥状光感受器的变性时间。这些研究已经导致了许多经 FDA 批准的临床试验的启动,用于应用细胞疗法治疗 AMD 和其他视网膜退行性疾病。然而,将啮齿动物模型直接转化为人体临床试验跳过了一个重要的临床前步骤,该步骤是解决眼内细胞移植的关键问题所必需的。这些问题包括确定最合适且最无问题的手术方法,在具有类似大小和结构的眼睛(包括黄斑)中应用治疗,以及充分了解关于移植物存活和移植物排斥的后果的免疫考虑因素。本章将回顾这些和相关问题,并记录当前解决这些问题的努力。