| Literature DB >> 20828776 |
Miho Murakami1, Hideyo Ugai, Minghui Wang, Natalya Belousova, Paul Dent, Paul B Fisher, Joel N Glasgow, Maaike Everts, David T Curiel.
Abstract
Human adenovirus serotype 5 (HAdV-5) attaches to its primary receptor, the coxsackie and adenovirus receptor (CAR) as the first step of infection. However, CAR expression decreases as tumors progress, thereby diminishing the utility of HAdV-5-based vectors for cancer therapy. In contrast, many aggressive tumor cells highly express CD46, a cellular receptor for HAdV-3. We hypothesized that a mosaic HAdV vector, containing two kinds of fiber proteins, would provide extensive transduction in a heterogeneous population of tumor cells with varying expression levels of HAdV receptors. We therefore generated a fiber-mosaic HAdV vector displaying both a chimeric HAdV-3 fiber and the HAdV-5 fiber protein. We verified the structural integrity of purified viral particles and confirmed that the fiber-mosaic HAdV vector has expanded tropism. We conclude that the use of fiber-mosaic HAdV vectors is a promising approach for transducing a heterogeneous cell population with different expression levels of adenovirus receptors. Published by Elsevier Inc.Entities:
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Year: 2010 PMID: 20828776 DOI: 10.1016/j.virol.2010.08.010
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616