Rhadinovirus vector-derived human telomerase reverse transcriptase expression in primary T cells

The rhadinovirus herpesvirus saimiri (HVS) as a gene delivery vector allows large DNA insertions and long-termed gene expression. In the case of T-cell transduction, such vectors use the viral transformation-associated genes of HVS C488 for T-cell amplification. In this report, we investigated wheth...

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Hauptverfasser: Toptan, Tuna (VerfasserIn) , Ensser, Armin (VerfasserIn) , Fickenscher, Helmut (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 18 February 2010
In: Gene therapy
Year: 2010, Jahrgang: 17, Heft: 5, Pages: 653-661
ISSN:1476-5462
DOI:10.1038/gt.2010.3
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1038/gt.2010.3
Verlag, lizenzpflichtig, Volltext: https://www.nature.com/articles/gt20103
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Verfasserangaben:T Toptan, A Ensser and H Fickenscher
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Zusammenfassung:The rhadinovirus herpesvirus saimiri (HVS) as a gene delivery vector allows large DNA insertions and long-termed gene expression. In the case of T-cell transduction, such vectors use the viral transformation-associated genes of HVS C488 for T-cell amplification. In this report, we investigated whether the gene for the catalytic telomerase subunit human telomerase reverse transcriptase (hTERT) can substitute for the transformation-associated genes in rhadinoviral T-cell transduction and amplification. By using virus mutants generated by en passant mutagenesis from bacterial artificial chromosomes, we observed a very early and functional transgene expression even by virus mutants without transformation-associated genes. The markers of T-cell transformation by HVS, namely CD2 hyperreactivity, overexpression of interleukin-26, and of the tyrosine kinase Lyn could neither be induced nor enhanced by ectopic hTERT expression. When the viral transformation-associated genes were replaced by the hTERT gene, it was not sufficient for growth transformation, although hTERT was efficiently transduced and functionally expressed by the rhadinovirus vector. Thus, the transformation-associated proteins StpC and Tip are responsible for the T-cell phenotype after transduction by HVS and, additionally, modulate telomerase activity independently of hTERT expression.
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Beschreibung:Online Resource
ISSN:1476-5462
DOI:10.1038/gt.2010.3