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Stem Cells. 2009 Jan;27(1):100-7. doi: 10.1634/stemcells.2008-0813.

Generation of T lineage cells from human embryonic stem cells in a feeder free system.

Author information

1
Department of Medicine, David Geffen School of Medicine, University of California, Los Angeles, 90095, USA. zgalic@ucla.edu

Abstract

Human embryonic stem cells (hESC) have the potential to revolutionize certain medical treatments, including T-cell-based therapies. However, optimal approaches to develop T cells from hESC are lacking. In this report, we show that T-cell progenitors can be derived from hESC cultured as embryoid bodies (EBs). These EB-derived T-cell progenitors give rise to phenotypically and functionally normal cells of the T lineage when transferred into human thymic tissue implanted in immunocompromised mice, suggesting that introduction of these progenitors into patients may also yield functional T cells. Moreover, hematopoietic progenitors demonstrating T-cell potential appeared to be CD45+/CD34+, resembling those found in normal bone marrow. In contrast to T cells developed from hESC cocultured on murine stromal cells, the EB-derived T cells also expressed normal levels of CD45. Importantly, the EB system eliminates the previous need for murine cocultures, a key impediment to developing a protocol for T-cell progenitor derivation suitable for clinical use. Furthermore, following lentiviral-mediated introduction of a vector expressing enhanced green fluorescent protein into hESC, stable transgene expression was maintained throughout differentiation, suggesting a potential for gene therapy approaches aimed at the augmentation of T-cell function or treatment of T-cell disorders.

PMID:
18974209
PMCID:
PMC2858464
DOI:
10.1634/stemcells.2008-0813
[Indexed for MEDLINE]
Free PMC Article

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