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Proteasome activity restricts lentiviral gene transfer into hematopoietic stem cells and is down-regulated by cytokines that enhance transduction

The therapeutic potential of hematopoietic stem cell (HSC) gene therapy can be fully exploited only by reaching efficient gene transfer into HSCs without compromising their biologic properties. Although HSCs can be transduced by HIV-derived lentiviral vectors (LVs) in short ex vivo culture, they dis...

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Autori principali: Santoni de Sio, Francesca Romana, Cascio, Paolo, Zingale, Anna, Gasparini, Mauro, Naldini, Luigi
Natura: Artigo
Lingua:Inglês
Pubblicazione: The American Society of Hematology 2006
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1464833/
https://ncbi.nlm.nih.gov/pubmed/16469870
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2005-10-4047
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