4.7 Article

Stable gene transfer and expression in human primary T cells by the Sleeping Beauty transposon system

Journal

BLOOD
Volume 107, Issue 2, Pages 483-491

Publisher

AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2005-05-2133

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Funding

  1. NCI NIH HHS [CO6 CA062526-01] Funding Source: Medline
  2. NIGMS NIH HHS [T32 GM08347] Funding Source: Medline
  3. PHS HHS [R01 52952] Funding Source: Medline

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The Sleeping Beauty (SB)transposon system is a nonviral DNA delivery system in which a transposase directs integration of an SB transposon into TA-dinucleotide sites in the genome. To determine whether the SB transposon system can mediate stable gene expression in human T cells, primary peripheral blood lymphocytes (PBLs) were nucleofected with SB vectors carrying a DsRed reporter gene. Plasmids containing the SB transposase on the same molecule as (cis) or on a molecule separate from (trans)the SB transposon mediated long-term and stable reporter gene expression in human primary T cells. Sequencing of transposon:chromosome junctions confirmed that stable gene expression was due to SB-mediated transposition. In other studies, PBLs were successfully transfected using the SB transposon system and shown to stably express a fusion protein consisting of (1) a surface receptor useful for positive T-cell selection and (2) a '' suicide '' gene useful for elimination of transfected T cells after chemotherapy. This study is the first report demonstrating that the SB transposon system can mediate stable gene transfer in human primary PBLs, which may be advantageous for T-cell-based gene therapies.

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