Dang Yalong, Zhang Chun, Zhu Yu
Department of Ophthalmology, Peking University Third Hospital, Beijing, People's Republic of China ; Clinical Stem Cell Research Center, Peking University Third Hospital, Beijing, People's Republic of China ; Department of Ophthalmology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, People's Republic of China.
Department of Ophthalmology, Peking University Third Hospital, Beijing, People's Republic of China ; Clinical Stem Cell Research Center, Peking University Third Hospital, Beijing, People's Republic of China.
Clin Interv Aging. 2015 Jan 14;10:255-64. doi: 10.2147/CIA.S73705. eCollection 2015.
In the developed world, age-related macular degeneration (AMD) is one of the major causes of irreversible blindness in the elderly. Although management of neovascular AMD (wet AMD) has dramatically progressed, there is still no effective treatment for nonneovascular AMD (dry AMD), which is characterized by retinal pigment epithelial (RPE) cell death (or dysfunction) and microenvironmental disruption in the retina. Therefore, RPE replacement and microenvironmental regulation represent viable treatments for dry AMD. Recent advances in cell biology have demonstrated that RPE cells can be easily generated from several cell types (pluripotent stem cells, multipotent stem cells, or even somatic cells) by spontaneous differentiation, coculturing, defined factors or cell reprogramming, respectively. Additionally, in vivo studies also showed that the restoration of visual function could be obtained by transplanting functional RPE cells into the subretinal space of recipient. More importantly, clinical trials approved by the US government have shown promising prospects in RPE transplantation. However, key issues such as implantation techniques, immune rejection, and xeno-free techniques are still needed to be further investigated. This review will summarize recent advances in cell transplantation for dry AMD. The obstacles and prospects in this field will also be discussed.
在发达国家,年龄相关性黄斑变性(AMD)是老年人不可逆失明的主要原因之一。尽管新生血管性AMD(湿性AMD)的治疗取得了显著进展,但对于以视网膜色素上皮(RPE)细胞死亡(或功能障碍)和视网膜微环境破坏为特征的非新生血管性AMD(干性AMD),仍然没有有效的治疗方法。因此,RPE替代和微环境调节是干性AMD可行的治疗方法。细胞生物学的最新进展表明,RPE细胞可以分别通过自发分化、共培养、特定因子或细胞重编程从几种细胞类型(多能干细胞、多能干细胞甚至体细胞)中轻松生成。此外,体内研究还表明,将功能性RPE细胞移植到受体的视网膜下间隙可以恢复视觉功能。更重要的是,美国政府批准的临床试验在RPE移植方面显示出了有前景的前景。然而,植入技术、免疫排斥和无动物源技术等关键问题仍需进一步研究。本综述将总结干性AMD细胞移植的最新进展。还将讨论该领域的障碍和前景。