Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/56131
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Type: Journal article
Title: Dual targeting of gene delivery by genetic modification of adenovirus serotype 5 fibers and cell-selective transcriptional control
Author: Work, L.
Ritchie, N.
Nicklin, S.
Reynolds, P.
Baker, A.
Citation: Gene Therapy (Basingstoke), 2004; 11(16):1296-1300
Publisher: Nature Publishing Group
Issue Date: 2004
ISSN: 0969-7128
1476-5462
Statement of
Responsibility: 
L M Work, N Ritchie, S A Nicklin, P N Reynolds and A H Baker
Abstract: Adenovirus (Ad)-mediated gene delivery is a promising approach for genetic manipulation of the vasculature and is being used in both preclinical models and clinical trials. However, safety concerns relating to infection of nontarget tissue and the poor infectivity of vascular cells compared to other cell types necessitates Ad vector refinement. Here, we combine a transductional targeting approach to improve vascular cell infectivity through RGD peptide insertion into adenovirus fibers, combined with transcriptional targeting to endothelial cells using a approximately 1 kb fragment of the fms-like tyrosine kinase receptor-1 (FLT-1) promoter. Single- and double-modified vectors were characterized in human cell lines that either support or have silenced FLT-1 expression. In rat hepatocytes and endothelial cells, the double modification substantially shifted transduction profiles toward vascular endothelial cells. Furthermore, in intact aortae derived from spontaneously hypertensive rats that display enhanced alphav integrin expression on dysfunctional endothelium, enhanced levels of transduction were observed using the double-modified vector but not in aortae derived from normotensive control rats. Our data indicate that Ad-mediated transduction can be beneficially modified in vitro and in vivo by combining fiber modification and a cell-selective promoter within a single-component vector system
Keywords: adenovirus
targeting
promoters
vascular disease
DOI: 10.1038/sj.gt.3302292
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