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日本未来基于胚胎干细胞疗法的研发战略

Research and Development Strategy for Future Embryonic Stem Cell-Based Therapy in Japan.

作者信息

Umezawa Akihiro, Sato Yoji, Kusakawa Shinji, Amagase Rin, Akutsu Hidenori, Nakamura Kazuaki, Kasahara Mureo, Matsubara Yoichi, Igarashi Takashi

机构信息

Center for Regenerative Medicine, National Center for Child Health and Development, Tokyo, Japan.

Division of Cell-Based Therapeutic Products, National Institute of Health Sciences, Kawasaki, Japan.

出版信息

JMA J. 2020 Oct 15;3(4):287-294. doi: 10.31662/jmaj.2018-0029. Epub 2020 Sep 23.

DOI:10.31662/jmaj.2018-0029
PMID:33225099
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7676987/
Abstract

Herewith, we review an updated progress of regenerative medical products using human embryonic stem cells (ESCs) in Japan. Two groups from Kyoto University and the National Center for Child Health and Development (NCCHD) established a novel derivation/cultivation system of ESCs for potential application in translational and clinical research. At the first stage of ESC derivation, murine feeder cells have been used in line with Japanese guidelines on public health associated with the implementation of the xenograft. To avoid exposure of ESCs to animal products in culture media, a xeno-free cultivating system has been established. Twelve ESCs (KhES-1, KhES-2, KhES-3, KhES-4, KhES-5, SEES-1, SEES-2, SEES-3, SEES-4, SEES-5, SEES-6, and SEES-7) are now available under a clinically relevant platform for industrially and clinically applicable regenerative medical products. NCCHD submitted an investigative new drug application to the Pharmaceuticals and Medical Devices Agency (PMDA) for using ESC-based products in patients with hyperammonemia due to genetic defects on March 2018 under the Pharmaceutical Affairs Law (now revised to the Pharmaceuticals, Medical Devices, and Other Therapeutic Products Act). Currently, up to ten ESC-based products are being prepared for intractable and rare disorders in Japan.

摘要

在此,我们回顾了日本使用人类胚胎干细胞(ESC)的再生医疗产品的最新进展。京都大学和国立儿童健康与发展中心(NCCHD)的两个团队建立了一种新型的ESC衍生/培养系统,用于转化和临床研究的潜在应用。在ESC衍生的第一阶段,根据日本与异种移植实施相关的公共卫生指南,使用了小鼠饲养细胞。为避免ESC在培养基中接触动物产品,已建立了无血清培养系统。目前,在一个临床相关平台上有12种ESC(KhES-1、KhES-2、KhES-3、KhES-4、KhES-5、SEES-1、SEES-2、SEES-3、SEES-4、SEES-5、SEES-6和SEES-7)可用于工业和临床适用的再生医疗产品。2018年3月,NCCHD根据《药事法》(现修订为《药品、医疗器械及其他治疗产品法》)向药品和医疗器械局(PMDA)提交了一份研究性新药申请,用于治疗因遗传缺陷导致高氨血症的患者使用基于ESC的产品。目前,日本正在为治疗难治性和罕见疾病准备多达十种基于ESC的产品。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/830f/7676987/027f1e49a71e/2433-3298-3-4-0287-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/830f/7676987/027f1e49a71e/2433-3298-3-4-0287-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/830f/7676987/027f1e49a71e/2433-3298-3-4-0287-g001.jpg

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A study on ensuring the quality and safety of pharmaceuticals and medical devices derived from processing of autologous human induced pluripotent stem(-like) cells.
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