Treatment of sickle cell anemia mouse model with iPS cells generated from autologous skin - PubMed (original) (raw)
. 2007 Dec 21;318(5858):1920-3.
doi: 10.1126/science.1152092. Epub 2007 Dec 6.
Affiliations
- PMID: 18063756
- DOI: 10.1126/science.1152092
Treatment of sickle cell anemia mouse model with iPS cells generated from autologous skin
Jacob Hanna et al. Science. 2007.
Abstract
It has recently been demonstrated that mouse and human fibroblasts can be reprogrammed into an embryonic stem cell-like state by introducing combinations of four transcription factors. However, the therapeutic potential of such induced pluripotent stem (iPS) cells remained undefined. By using a humanized sickle cell anemia mouse model, we show that mice can be rescued after transplantation with hematopoietic progenitors obtained in vitro from autologous iPS cells. This was achieved after correction of the human sickle hemoglobin allele by gene-specific targeting. Our results provide proof of principle for using transcription factor-induced reprogramming combined with gene and cell therapy for disease treatment in mice. The problems associated with using retroviruses and oncogenes for reprogramming need to be resolved before iPS cells can be considered for human therapy.
Comment in
- Development. Is therapeutic cloning dead?
Cibelli J. Cibelli J. Science. 2007 Dec 21;318(5858):1879-80. doi: 10.1126/science.1153229. Science. 2007. PMID: 18096796 No abstract available.
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