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Journal of Virology, November 2001, p. 10393-10400, Vol. 75, No. 21
Gene Therapy Program,1
Department of Medicine,2
Department of Pediatrics,4 and
Department of Anatomy,5 Louisiana State
University Health Sciences Center of New Orleans, and Bone
Marrow Transplantation Program, Tulane
University,3 New Orleans, Louisiana
Received 11 July 2001/Accepted 16 July 2001
We have previously reported effective gene transfer with a targeted
molecular conjugate adenovirus vector through the c-kit receptor in
hematopoietic progenitor cell lines. However, a c-kit-targeted recombinant retroviral vector failed to transduce cells,
indicating the existence of significant differences for c-kit target
gene transfer between these two viruses. Here we demonstrate
that conjugation of an adenovirus to a c-kit-retargeted
retrovirus vector enables retroviral transduction. This finding
suggests the requirement of endosomalysis for successful c-kit-targeted
gene transfer. Furthermore, we show efficient gene transfer to, and
high transgene expression (66%) in, CD34-selected,
c-kit+ human peripheral blood stem cells using a
c-kit-targeted adenovirus vector. These findings may have important
implications for future vector development in c-kit-targeted stem cell
gene transfer.
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.21.10393-10400.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Efficient c-kit Receptor-Targeted Gene Transfer to
Primary Human CD34-Selected Hematopoietic Stem Cells
*
Corresponding author. Mailing address: Gene Therapy
Program, LSUHSC, 533 Bolivar St., CRSB, Room 611, New Orleans, LA
70112. Phone: (504) 568-6294. Fax: (504) 568-8500. E-mail:
PSCHWA1{at}LSUHSC.EDU.
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