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Hematopoietic vs Embryonic Sources for Stem Cell Research

Steven Teitelbaum, MD; Shane Smith, PhD; William Neaves, PhD
JAMA. 2008;299(23):2746-2747. doi:10.1001/jama.299.23.2746-b
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To the Editor: In their Clinical Review, Dr Burt and colleagues1 assessed clinical applications of adult stem cell therapies for nonmalignant diseases. They acknowledge modest benefit from hematopoietic stem cell transplantation in cardiac disease and ameliorative but noncurative outcomes in autoimmune diseases. Although we agree that greater investments are needed in the clinical development of these therapies, we disagree with the authors' suggestion that, relative to embryonic stem cells, adult stem cells provide a superior vehicle for cell-based therapies because they lack tumorigenic activity, can be prepared by methods approved by the Food and Drug Administration (FDA), and have been free of ethical controversy. It would have been more appropriate to note that their review targeted hematopoietic stem cell transplantation because embryonic stem cells are not yet ready for clinical use.

Their conclusion discounts reports of improving preparative methods for embryonic stem cells that may lend themselves to future FDA-approvable techniques.2 As the authors' research illustrates, adult stem cell research has flourished since its inception in the 1960s. The use of human embryonic stem cells, first derived in 1998, deserves similar time to assess its effectiveness. One kind of stem cell research does not obviate the need for the other. The spectrum of diseases affecting patients requires a broad-based approach to stem cell research, including the study of human embryonic stem cells as well as adult stem cells.

AUTHOR INFORMATION

Financial Disclosures: Drs Teitelbaum and Neaves reported membership in the Missouri Coalition for Lifesaving Cures. Dr Smith reported having been science director for Californians for Stem Cell Research & Cures, a consultant for the University of California Irvine Stem Cell Research Center, and a senior science advisor for Genetics Policy Institute and being science director for the Children's Neurobiological Solutions Foundation.

REFERENCES

Burt RK, Loh Y, Pearce W,  et al.  Clinical applications of blood-derived and marrow-derived stem cells for nonmalignant diseases.  JAMA. 2008;299(8):925-935
PubMedCrossRef
Phillips BW, Lim RYM, Tan TT, Rust WL, Crook JM. Efficient expansion of clinical-grade human fibroblasts on microcarriers: cells suitable for ex vivo expansion of clinical-grade hESCs.  J Biotechnol. 2008;134(1-2):79-87
PubMedCrossRef

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Burt RK, Loh Y, Pearce W,  et al.  Clinical applications of blood-derived and marrow-derived stem cells for nonmalignant diseases.  JAMA. 2008;299(8):925-935
PubMedCrossRef
Phillips BW, Lim RYM, Tan TT, Rust WL, Crook JM. Efficient expansion of clinical-grade human fibroblasts on microcarriers: cells suitable for ex vivo expansion of clinical-grade hESCs.  J Biotechnol. 2008;134(1-2):79-87
PubMedCrossRef
June 18, 2008
Richard Burt, MD; John Kessler, MD; Yvonne Loh, MD
JAMA. 2008;299(23):2746-2747.
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