Author contributions: M.R., L.A.R., and D.S.K.: conception and design, manuscript writing, and final approval of manuscript.
Embryonic Stem Cells/Induced Pluripotent Stem Cells
Concise Review: Cord Blood Banking, Transplantation and Induced Pluripotent Stem Cell: Success and Opportunities
Article first published online: 28 DEC 2011
DOI: 10.1002/stem.770
Copyright © 2011 AlphaMed Press
Additional Information
How to Cite
Rao, M., Ahrlund-Richter, L. and Kaufman, D. S. (2012), Concise Review: Cord Blood Banking, Transplantation and Induced Pluripotent Stem Cell: Success and Opportunities. STEM CELLS, 30: 55–60. doi: 10.1002/stem.770
- †
Author contributions: M.R., L.A.R., and D.S.K.: conception and design, manuscript writing, and final approval of manuscript.
- ‡
Disclosure of potential conflicts of interest is found at the end of this article.
- §
First published online in STEM CELLSEXPRESS November 8, 2011. available online without subscription through the open access option.
Publication History
- Issue published online: 28 DEC 2011
- Article first published online: 28 DEC 2011
- Accepted manuscript online: 8 NOV 2011 04:56PM EST
- Manuscript Accepted: 13 OCT 2011
- Manuscript Received: 30 JUN 2011
Funded by
- CIRM and Maryland TEDCO
- NIH/NHLBI
- Abstract
- Article
- References
- Cited By
Keywords:
- Hematopoietic stem cell transplantation;
- Hematologic malignancies;
- Bone marrow;
- Cord blood
Abstract
Hematopoietic cell transplantation (HCT) has become a standard practice to treat a number of malignant and nonmalignant hematologic diseases. Bone marrow, mobilized peripheral blood, and umbilical cord blood can all serve as primary sources of cells for HCT. The number of cord blood units currently stored is large, although it represents only a fraction of potential collections. With much of the collection being sequestered in private banks for possible autologous use, there is a reason to expect that public banks may not be able to provide for the demand in coming years as use of cord blood for treatment of patients with diseases such as leukemia and lymphoma continues to increase. We suggest that a possible solution to encourage private banks to share their valuable units is to apply recent methodologies to generate induced pluripotent stem cells from cord cells and to optimize techniques to generate hematopoietic lineages from them. This strategy would allow us to take advantage of the units already collected under appropriate regulatory guidelines, to access a pristine cell that can be converted to a pluripotent cell at a much higher efficiency and in a shorter time period than other cells. The ability to potentially replenish a used cord unit with new cells, as well as extend the potential utility of cord blood for additional therapeutic applications, should allow banks to develop an appropriate business model for both private and public cord blood banks to flourish. STEM CELLS2012;30:55–60

1549-4918/asset/olbannerleft.jpg?v=1&s=699114e871887e6b838f6a1c657fe256cfe127a6)
1549-4918/asset/olbannerright.gif?v=1&s=603f8f2ab5cd9d4f783c231915608956af51aeea)
