Quality Control Guidelines for Clinical-Grade Human Induced Pluripotent Stem Cell Lines

Stephen Sullivan, Glyn Stacey, Chihiro Akazawa(Tokyo Medical and Dental University), Naoki Aoyama(Japan Agency for Medical Research and Development), Ricardo P. Baptista(Guy's Hospital), Patrick Bedford, Annelise Bennaceur‐Griscelli(Université Paris-Sud), Amit Chandra(Loughborough University), Ngaire Elwood(The University of Melbourne), Mathilde Girard, Shin Kawamata(Foundation for Biomedical Research and Innovation), Tadaaki Hanatani(Kyoto University), Theodoros Latsis(Université Paris-Sud), Stephen Lin(California Institute for Regenerative Medicine), Tenneille E. Ludwig(WiCell), Tamara Malygina, Amanda A. Mack(Fujifilm (United States)), Joanne C. Mountford(Scottish National Blood Transfusion Service), Scott Noggle(New York Stem Cell Foundation), Lygia V. Pereira(Universidade de São Paulo), Jack Price(National Institute for Biological Standards and Control), Michael Sheldon(Rutgers, The State University of New Jersey), Alok Srivastava(Christian Medical College, Vellore), Harald Stachelscheid(Berlin Institute of Health at Charité - Universitätsmedizin Berlin), Shaji R Velayudhan(Christian Medical College, Vellore), Natalie J Ward(Guy's Hospital), Marc L. Turner(Guy's Hospital), Jacqueline Barry(Guy's Hospital), Jihwan Song(CHA University)
Regenerative Medicine
September 12, 2018
Cited by 276Open Access
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Abstract

Use of clinical-grade human induced pluripotent stem cell (iPSC) lines as a starting material for the generation of cellular therapeutics requires demonstration of comparability of lines derived from different individuals and in different facilities. This requires agreement on the critical quality attributes of such lines and the assays that should be used. Working from established recommendations and guidance from the International Stem Cell Banking Initiative for human embryonic stem cell banking, and concentrating on those issues more relevant to iPSCs, a series of consensus workshops has made initial recommendations on the minimum dataset required to consider an iPSC line of clinical grade, which are outlined in this report. Continued evolution of this field will likely lead to revision of these guidelines on a regular basis.


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