Takahashi Jun
Department of Clinical Application, Center for iPS Cell Research and Application, Kyoto University, 53 Shogoin Kawahara-cho, Sakyo, Kyoto, 606-8507, Japan.
Regen Ther. 2020 Sep 15;13:18-22. doi: 10.1016/j.reth.2020.06.002. eCollection 2020 Mar.
Following intensive efforts since their discovery little more than 10 years ago, cell replacement therapy using induced pluripotent stem (iPS) cells is now becoming reality. However, there remain several obstacles in the translation of basic research to clinical application, obstacles known as the "Valley of Death". With regards to regenerative medicine using iPS cells for Parkinson's disease, we have developed a method for the 1) efficient induction of dopaminergic neurons from human iPS cells and 2) sorting dopaminergic progenitor cells using a floor plate marker, CORIN. The grafted CORIN cells survived well and functioned as midbrain dopaminergic neurons in the Parkinson's disease model rats and monkeys, and showed minimal risk of tumor formation. Based on these results, we performed a pre-clinical study using a clinical-grade iPS cell line and finally started a clinical trial to treat Parkinson's disease patients in August 2018. Here, I discuss the key issues to crossing the Valley of Death: scientific rationale, pre-clinical study, and clinical trial.
在10多年前发现诱导多能干细胞(iPS细胞)后经过深入研究,如今利用iPS细胞进行细胞替代疗法已成为现实。然而,基础研究转化为临床应用仍存在若干障碍,即所谓的“死亡谷”。关于使用iPS细胞治疗帕金森病的再生医学,我们开发了一种方法,可用于1)从人iPS细胞高效诱导多巴胺能神经元,以及2)使用底板标志物CORIN对多巴胺能祖细胞进行分选。移植的CORIN细胞在帕金森病模型大鼠和猴子体内存活良好,并发挥中脑多巴胺能神经元的功能,且肿瘤形成风险极小。基于这些结果,我们使用临床级iPS细胞系进行了临床前研究,并最终于2018年8月启动了治疗帕金森病患者的临床试验。在此,我将讨论跨越“死亡谷”的关键问题:科学原理、临床前研究和临床试验。