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用于晚期干性年龄相关性黄斑变性的生物工程视网膜色素上皮单层。

A bioengineered retinal pigment epithelial monolayer for advanced, dry age-related macular degeneration.

机构信息

University of Southern California (USC) Roski Eye Institute, USC Institute for Biomedical Therapeutics, and Department of Ophthalmology, Keck School of Medicine, USC, 1450 San Pablo, Los Angeles, CA 90033, USA.

Regenerative Patch Technologies, 150 Gabarda Way, Portola Valley, CA 94028-7445, USA.

出版信息

Sci Transl Med. 2018 Apr 4;10(435). doi: 10.1126/scitranslmed.aao4097.

Abstract

Retinal pigment epithelium (RPE) dysfunction and loss are a hallmark of non-neovascular age-related macular degeneration (NNAMD). Without the RPE, a majority of overlying photoreceptors ultimately degenerate, leading to severe, progressive vision loss. Clinical and histological studies suggest that RPE replacement strategies may delay disease progression or restore vision. A prospective, interventional, U.S. Food and Drug Administration-cleared, phase 1/2a study is being conducted to assess the safety and efficacy of a composite subretinal implant in subjects with advanced NNAMD. The composite implant, termed the California Project to Cure Blindness-Retinal Pigment Epithelium 1 (CPCB-RPE1), consists of a polarized monolayer of human embryonic stem cell-derived RPE (hESC-RPE) on an ultrathin, synthetic parylene substrate designed to mimic Bruch's membrane. We report an interim analysis of the phase 1 cohort consisting of five subjects. Four of five subjects enrolled in the study successfully received the composite implant. In all implanted subjects, optical coherence tomography imaging showed changes consistent with hESC-RPE and host photoreceptor integration. None of the implanted eyes showed progression of vision loss, one eye improved by 17 letters and two eyes demonstrated improved fixation. The concurrent structural and functional findings suggest that CPCB-RPE1 may improve visual function, at least in the short term, in some patients with severe vision loss from advanced NNAMD.

摘要

视网膜色素上皮 (RPE) 功能障碍和丧失是非新生血管性年龄相关性黄斑变性 (NNAMD) 的一个标志。没有 RPE,大部分位于其上的光感受器最终会退化,导致严重的、进行性的视力丧失。临床和组织学研究表明,RPE 替代策略可能会延缓疾病进展或恢复视力。正在进行一项前瞻性、干预性、美国食品和药物管理局批准的、1/2a 期的研究,以评估一种复合视网膜下植入物在晚期 NNAMD 患者中的安全性和疗效。这种复合植入物被称为加利福尼亚治愈失明-视网膜色素上皮 1 项目 (CPCB-RPE1),由一层极化的人胚胎干细胞衍生的 RPE(hESC-RPE)组成,位于超薄的合成聚对二甲苯基质上,旨在模拟布鲁赫膜。我们报告了一项由五名受试者组成的 1 期队列的中期分析。研究中纳入的五名受试者中有四名成功接受了复合植入物。在所有接受植入的受试者中,光学相干断层扫描成像显示与 hESC-RPE 和宿主光感受器整合一致的变化。植入的眼睛均未出现视力丧失进展,一只眼睛提高了 17 个字母,两只眼睛的固视得到改善。同时的结构和功能发现表明,CPCB-RPE1 可能至少在短期内改善一些严重视力丧失的晚期 NNAMD 患者的视觉功能。

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