Stem cell-based therapies for retinal diseases: focus on clinical trials and future prospects.

IF 1.2 4区 医学 Q4 GENETICS & HEREDITY
Sagnik Sen, Thales Antonio Cabral de Guimaraes, Aluisio Gameiro Filho, Lorenzo Fabozzi, Rachael A Pearson, Michel Michaelides
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Abstract

Stem cell-based therapy has gained importance over the past decades due to huge advances in science and technology behind the generation and directed differentiation of pluripotent cells from embryos and adult cells. Preclinical proof-of-concept studies have been followed by clinical trials showing efficacy and safety of transplantation of stem cell-based therapy, which are beginning to establish this as a modality of treatment. Disease candidates of interest are primarily conditions that may benefit from replacing dead or dying cells, including advanced inherited retinal dystrophies and age-related macular degeneration, and predominantly seek to transplant either RPE or photoreceptors, although neurotrophic approaches have also been trialed. Whilst a consensus has yet to be reached about the best stage/type of cells for transplantation (stem cells, progenitor cells, differentiated RPE and photoreceptors) and the methods of implantation (sheet, suspension), several CTs have shown safety. There remain potential concerns regarding tumorigenicity and immune rejection; however, with ongoing improvements in cell generation, selection, and delivery, these can be minimized. Earlier studies showed efficacy with immunosuppressive drugs to prevent rejection, and recent donor-matched transplants have avoided the need for immunosuppression. Retinal regenerative medicine is a challenging field and is in a nascent stage but holds tremendous promise. This narrative review delves into the current understanding of stem cells and the latest clinical trials of retinal cell transplantation.

基于干细胞的视网膜疾病疗法:临床试验重点与未来展望。
由于从胚胎和成体细胞中生成多能细胞并进行定向分化的科学和技术取得了巨大进步,干细胞疗法在过去几十年里变得越来越重要。临床前概念验证研究之后,临床试验显示了干细胞移植疗法的有效性和安全性,并开始将其确立为一种治疗方式。受关注的候选疾病主要是可从替换死亡或垂死细胞中获益的疾病,包括晚期遗传性视网膜营养不良症和老年性黄斑变性,主要寻求移植RPE或光感受器,尽管神经营养方法也已试用。虽然关于移植细胞的最佳阶段/类型(干细胞、祖细胞、分化的RPE和光感受器)和植入方法(片状、悬浮)尚未达成共识,但一些CT已显示出安全性。不过,随着细胞生成、筛选和输送技术的不断改进,这些问题都能得到最大程度的解决。早期的研究表明,使用免疫抑制药物可有效防止排斥反应,而最近的供体配型移植则避免了免疫抑制的需要。视网膜再生医学是一个极具挑战性的领域,目前尚处于起步阶段,但前景广阔。这篇叙述性综述深入探讨了目前对干细胞的理解以及视网膜细胞移植的最新临床试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Ophthalmic Genetics
Ophthalmic Genetics 医学-眼科学
CiteScore
2.40
自引率
8.30%
发文量
126
审稿时长
>12 weeks
期刊介绍: Ophthalmic Genetics accepts original papers, review articles and short communications on the clinical and molecular genetic aspects of ocular diseases.
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