Liu Hui, Lu Shuaiyan, Chen Ming, Gao Na, Yang Yuhe, Hu Huijuan, Ren Qing, Liu Xiaoyu, Chen Hongxu, Zhu Qunyan, Li Shasha, Su Jianzhong
National Engineering Research Center of Ophthalmology and Optometry, Eye Hospital, Wenzhou Medical University, Wenzhou, 325027, China.
State Key Laboratory of Ophthalmology, Optometry and Visual Science, Eye Hospital, Wenzhou Medical University, Wenzhou, 325027, China.
Stem Cell Rev Rep. 2024 Aug;20(6):1459-1479. doi: 10.1007/s12015-024-10740-4. Epub 2024 May 29.
Retinal degeneration (RD) is a leading cause of blindness worldwide and includes conditions such as retinitis pigmentosa (RP), age-related macular degeneration (AMD), and Stargardt's disease (STGD). These diseases result in the permanent loss of vision due to the progressive and irreversible degeneration of retinal cells, including photoreceptors (PR) and the retinal pigment epithelium (RPE). The adult human retina has limited abilities to regenerate and repair itself, making it challenging to achieve complete self-replenishment and functional repair of retinal cells. Currently, there is no effective clinical treatment for RD. Stem cell therapy, which involves transplanting exogenous stem cells such as retinal progenitor cells (RPCs), embryonic stem cells (ESCs), induced pluripotent stem cells (iPSCs), and mesenchymal stem cells (MSCs), or activating endogenous stem cells like Müller Glia (MG) cells, holds great promise for regenerating and repairing retinal cells in the treatment of RD. Several preclinical and clinical studies have shown the potential of stem cell-based therapies for RD. However, the clinical translation of these therapies for the reconstruction of substantial vision still faces significant challenges. This review provides a comprehensive overview of stem/progenitor cell-based therapy strategies for RD, summarizes recent advances in preclinical studies and clinical trials, and highlights the major challenges in using stem/progenitor cell-based therapies for RD.
视网膜变性(RD)是全球范围内导致失明的主要原因,包括色素性视网膜炎(RP)、年龄相关性黄斑变性(AMD)和斯塔加特病(STGD)等病症。这些疾病由于视网膜细胞(包括光感受器(PR)和视网膜色素上皮(RPE))的进行性和不可逆变性而导致永久性视力丧失。成年人类视网膜自我再生和修复的能力有限,因此实现视网膜细胞的完全自我补充和功能修复具有挑战性。目前,尚无针对RD的有效临床治疗方法。干细胞疗法,包括移植外源性干细胞,如视网膜祖细胞(RPC)、胚胎干细胞(ESC)、诱导多能干细胞(iPSC)和间充质干细胞(MSC),或激活内源性干细胞,如穆勒胶质(MG)细胞,在治疗RD中对视网膜细胞的再生和修复具有巨大潜力。多项临床前和临床研究表明了基于干细胞的疗法治疗RD的潜力。然而,这些疗法用于重建显著视力的临床转化仍面临重大挑战。本综述全面概述了基于干细胞/祖细胞的RD治疗策略,总结了临床前研究和临床试验的最新进展,并强调了使用基于干细胞/祖细胞的疗法治疗RD的主要挑战。