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Generation of clinical-grade human induced pluripotent stem cells in Xeno-free conditions

INTRODUCTION: Human induced pluripotent stem cells (hiPSCs) are considered as one of the most promising seed cell sources in regenerative medicine. Now hiPSC-based clinical trials are underway. To ensure clinical safety, cells used in clinical trials or therapies should be generated under GMP condit...

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Autores principales: Wang, Juan, Hao, Jie, Bai, Donghui, Gu, Qi, Han, Weifang, Wang, Lei, Tan, Yuanqing, Li, Xia, Xue, Ke, Han, Pencheng, Liu, Zhengxin, Jia, Yundan, Wu, Jun, Liu, Lei, Wang, Liu, Li, Wei, Liu, Zhonghua, Zhou, Qi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4643509/
https://www.ncbi.nlm.nih.gov/pubmed/26564165
http://dx.doi.org/10.1186/s13287-015-0206-y
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author Wang, Juan
Hao, Jie
Bai, Donghui
Gu, Qi
Han, Weifang
Wang, Lei
Tan, Yuanqing
Li, Xia
Xue, Ke
Han, Pencheng
Liu, Zhengxin
Jia, Yundan
Wu, Jun
Liu, Lei
Wang, Liu
Li, Wei
Liu, Zhonghua
Zhou, Qi
author_facet Wang, Juan
Hao, Jie
Bai, Donghui
Gu, Qi
Han, Weifang
Wang, Lei
Tan, Yuanqing
Li, Xia
Xue, Ke
Han, Pencheng
Liu, Zhengxin
Jia, Yundan
Wu, Jun
Liu, Lei
Wang, Liu
Li, Wei
Liu, Zhonghua
Zhou, Qi
author_sort Wang, Juan
collection PubMed
description INTRODUCTION: Human induced pluripotent stem cells (hiPSCs) are considered as one of the most promising seed cell sources in regenerative medicine. Now hiPSC-based clinical trials are underway. To ensure clinical safety, cells used in clinical trials or therapies should be generated under GMP conditions, and with Xeno-free culture media to avoid possible side effects like immune rejection that induced by the Xeno reagents. However, up to now there are no reports for hiPSC lines developed completely under GMP conditions using Xeno-free reagents. METHODS: Clinical-grade human foreskin fibroblast (HFF) cells used as feeder cells and parental cells of the clinical-grade hiPSCs were isolated from human foreskin tissues and cultured in Xeno-free media. Clinical-grade hiPSCs were derived by integration-free Sendai virus-based reprogramming kit in Xeno-free pluriton™ reprogramming medium or X medium. Neural cells and cardiomyocytes differentiation were conducted following a series of spatial and temporal specific signals induction according to the corresponding lineage development signals. Biological safety evaluation of the clinical-grade HFF cells and hiPSCs were conducted following the guidance of the “Pharmacopoeia of the People's Republic of China, Edition 2010, Volume III”. RESULTS: We have successfully derived several integration-free clinical-grade hiPSC lines under GMP-controlled conditions and with Xeno-free reagents culture media in line with the current guidance of international and national evaluation criteria. As for the source of hiPSCs and feeder cells, biological safety evaluation of the HFF cells have been strictly reviewed by the National Institutes for Food and Drug Control (NIFDC). The hiPSC lines are pluripotent and have passed the safety evaluation. Moreover, one of the randomly selected hiPSC lines was capable of differentiating into functional neural cells and cardiomyocytes in Xeno-free culture media. CONCLUSION: The clinical-grade hiPSC lines therefore could be valuable sources for future hiPSC-based clinical trials or therapies and for drug screening. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13287-015-0206-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-46435092015-11-14 Generation of clinical-grade human induced pluripotent stem cells in Xeno-free conditions Wang, Juan Hao, Jie Bai, Donghui Gu, Qi Han, Weifang Wang, Lei Tan, Yuanqing Li, Xia Xue, Ke Han, Pencheng Liu, Zhengxin Jia, Yundan Wu, Jun Liu, Lei Wang, Liu Li, Wei Liu, Zhonghua Zhou, Qi Stem Cell Res Ther Research INTRODUCTION: Human induced pluripotent stem cells (hiPSCs) are considered as one of the most promising seed cell sources in regenerative medicine. Now hiPSC-based clinical trials are underway. To ensure clinical safety, cells used in clinical trials or therapies should be generated under GMP conditions, and with Xeno-free culture media to avoid possible side effects like immune rejection that induced by the Xeno reagents. However, up to now there are no reports for hiPSC lines developed completely under GMP conditions using Xeno-free reagents. METHODS: Clinical-grade human foreskin fibroblast (HFF) cells used as feeder cells and parental cells of the clinical-grade hiPSCs were isolated from human foreskin tissues and cultured in Xeno-free media. Clinical-grade hiPSCs were derived by integration-free Sendai virus-based reprogramming kit in Xeno-free pluriton™ reprogramming medium or X medium. Neural cells and cardiomyocytes differentiation were conducted following a series of spatial and temporal specific signals induction according to the corresponding lineage development signals. Biological safety evaluation of the clinical-grade HFF cells and hiPSCs were conducted following the guidance of the “Pharmacopoeia of the People's Republic of China, Edition 2010, Volume III”. RESULTS: We have successfully derived several integration-free clinical-grade hiPSC lines under GMP-controlled conditions and with Xeno-free reagents culture media in line with the current guidance of international and national evaluation criteria. As for the source of hiPSCs and feeder cells, biological safety evaluation of the HFF cells have been strictly reviewed by the National Institutes for Food and Drug Control (NIFDC). The hiPSC lines are pluripotent and have passed the safety evaluation. Moreover, one of the randomly selected hiPSC lines was capable of differentiating into functional neural cells and cardiomyocytes in Xeno-free culture media. CONCLUSION: The clinical-grade hiPSC lines therefore could be valuable sources for future hiPSC-based clinical trials or therapies and for drug screening. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13287-015-0206-y) contains supplementary material, which is available to authorized users. BioMed Central 2015-11-12 /pmc/articles/PMC4643509/ /pubmed/26564165 http://dx.doi.org/10.1186/s13287-015-0206-y Text en © Wang et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Wang, Juan
Hao, Jie
Bai, Donghui
Gu, Qi
Han, Weifang
Wang, Lei
Tan, Yuanqing
Li, Xia
Xue, Ke
Han, Pencheng
Liu, Zhengxin
Jia, Yundan
Wu, Jun
Liu, Lei
Wang, Liu
Li, Wei
Liu, Zhonghua
Zhou, Qi
Generation of clinical-grade human induced pluripotent stem cells in Xeno-free conditions
title Generation of clinical-grade human induced pluripotent stem cells in Xeno-free conditions
title_full Generation of clinical-grade human induced pluripotent stem cells in Xeno-free conditions
title_fullStr Generation of clinical-grade human induced pluripotent stem cells in Xeno-free conditions
title_full_unstemmed Generation of clinical-grade human induced pluripotent stem cells in Xeno-free conditions
title_short Generation of clinical-grade human induced pluripotent stem cells in Xeno-free conditions
title_sort generation of clinical-grade human induced pluripotent stem cells in xeno-free conditions
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4643509/
https://www.ncbi.nlm.nih.gov/pubmed/26564165
http://dx.doi.org/10.1186/s13287-015-0206-y
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