Hurdles to clinical translation of human induced pluripotent stem cells

被引:122
作者
Neofytou, Evgenios [1 ,2 ,3 ]
O'Brien, Connor Galen [1 ,3 ]
Couture, Larry A. [4 ]
Wu, Joseph C. [1 ,2 ,3 ]
机构
[1] Stanford Univ, Sch Med, Stanford Cardiovasc Inst, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Inst Stem Cell Biol & Regenerat Med, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Med, Div Cardiol, Stanford, CA 94305 USA
[4] City Hope Natl Med Ctr, Beckman Res Inst, Duarte, CA 91010 USA
关键词
GOOD MANUFACTURING PRACTICE; IPS CELLS; THERAPIES; LINES; GENE; TRACKING; DONOR; BANK; CARDIOMYOCYTES; PROGENITORS;
D O I
10.1172/JCI80575
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Human pluripotent stem cells are known to have the capacity to renew indefinitely, being intrinsically able to differentiate into many different cell types. These characteristics have generated tremendous enthusiasm about the potential applications of these cells in regenerative medicine. However, major challenges remain with the development and testing of novel experimental stem cell therapeutics in the field. In this Review, we focus on the nature of the preclinical challenges and discuss potential solutions that could help overcome them. Furthermore, we discuss the use of allogeneic versus autologous stem cell products, including a review of their respective advantages and disadvantages, major clinical requirements, quality standards, time lines, and costs of clinical grade development.
引用
收藏
页码:2551 / 2557
页数:7
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