Qiu Tina Guanting
Ophthalmic Therapeutic Innovation, Boston, MA USA.
NPJ Regen Med. 2019 Aug 27;4:19. doi: 10.1038/s41536-019-0081-8. eCollection 2019.
The use of human embryonic stem cell (hESC)-derived Retinal Pigment Epithelium (RPE) transplants has advanced dramatically in different forms for clinical application in macular degeneration. This review focuses on the first generation of hESC-RPE cell line, named as "MA09-hRPE" by Astellas Institute of Regenerative Medicine (AIRM), and its therapeutic application in human, which evaluated the safety and efficacy of MA09-hRPE cell line transplanted in patients with macular degeneration. This project marks the first milestone in overcoming ethical hurdles and oncogenic safety concerns associated with the use of an embryonic stem cell-derived line. Through in-depth, evidence-based analysis of the MA09-hRPE cell line, along with other hESC-RPE cell lines, this review aims to draw attention to the key technical challenges pertinent to the generation of a biologically competent hESC-RPE cell line and distill the four key prognostic factors residing in the host retina, which concurrently determine the outcomes of clinical efficacy and visual benefits. Given that the technology is still at its infancy for human use, a new clinical regulatory path could aid in cell line validation through small cohort, adaptive clinical trials to accelerate product development toward commercialization. These strategic insights will be invaluable to help both academia and industry, collaboratively shorten the steep learning curve, and reduce large development expenditures spent on unnecessary lengthy clinical trials.
人胚胎干细胞(hESC)来源的视网膜色素上皮(RPE)移植在黄斑变性临床应用的不同形式上取得了显著进展。本综述聚焦于再生医学阿斯特拉研究所(AIRM)命名为“MA09-hRPE”的第一代hESC-RPE细胞系及其在人体中的治疗应用,该研究评估了MA09-hRPE细胞系移植到黄斑变性患者体内的安全性和有效性。该项目标志着在克服与使用胚胎干细胞衍生系相关的伦理障碍和致癌安全性问题方面迈出了第一个里程碑。通过对MA09-hRPE细胞系以及其他hESC-RPE细胞系进行深入的循证分析,本综述旨在提请关注与生成具有生物学活性的hESC-RPE细胞系相关的关键技术挑战,并提炼出宿主视网膜中的四个关键预后因素,这些因素共同决定临床疗效和视觉益处的结果。鉴于该技术在人类应用方面仍处于起步阶段,一条新的临床监管途径可通过小型队列适应性临床试验帮助验证细胞系,以加速产品开发走向商业化。这些战略见解对于帮助学术界和产业界共同缩短陡峭的学习曲线、减少在不必要的冗长临床试验上的大量开发支出将具有不可估量的价值。