| Literature DB >> 25770678 |
Hongyan Zhou1, Mahendra S Rao2.
Abstract
The discovery of induced pluripotent stem cells (iPSCs) and the rapid evolution of clinically compliant protocols to generate such lines from a variety of tissue sources has raised the possibility that personalized medicine may be achievable in the near future. Several strategies to deliver iPSCs for iPSC-derived cell-based therapy have been proposed: one such model has been the cell-banking model, using processes developed by the cord blood industry. The cord blood industry has evolved primarily as a banking model in which units of cord blood harvested from discarded placenta are stored either in a public or a private cord blood bank for future use. The consideration of a cord blood--like banking model has been further spurred by the realization that this population of cells is an ideal starting sample to generate pluripotent cells. Spurred by these technological advances, major efforts are underway to develop a current Good Manufacturing Practice--compliant protocol to generate iPSCs from cord blood and to develop a haplobanking strategy. In this article, we discuss the issues that may affect such an effort.Keywords: cGMP; consent; cord blood; embryonic stem cells; induced pluripotent stem cells; manufacturing; markers
Mesh:
Year: 2015 PMID: 25770678 DOI: 10.1016/j.jcyt.2015.02.008
Source DB: PubMed Journal: Cytotherapy ISSN: 1465-3249 Impact factor: 5.414