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pubmed-article:16271741pubmed:abstractTextWe recently showed that both replicating and resting cells cultivated with ganciclovir (GCV) were killed when challenged with vesicular stomatitis virus G glycoprotein pseudotyped HIV-1-based virus-like particles (VLPs) carrying the Nef7 (i.e., an HIV-1 Nef mutant incorporating in virions at high levels)/herpes simplex virus-1 thymidine kinase (HSV-TK) fusion product. On this basis, a novel anti-HIV therapeutic approach based on Nef7/TK VLPs expressing X4 or R5 HIV cell receptor complexes has been attempted. We here report that (CD4-CXCR4) and (CD4-CCR5) Nef7-based VLPs efficiently enter cells infected by X4- or R5-tropic HIV-1 strains, respectively. Importantly, the delivery of the VLP-associated Nef7/TK led to cell death upon GCV treatment. Of interest, VLPs were effective also against non-replicating, HIV-1-infected primary human monocyte-derived macrophages. HIV-targeted VLPs represent a promising candidate for the treatment of persistently HIV-1-infected cells that are part of virus reservoirs resistant to HAART therapies.lld:pubmed
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pubmed-article:16271741pubmed:pagination115-26lld:pubmed
pubmed-article:16271741pubmed:dateRevised2007-11-15lld:pubmed
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pubmed-article:16271741pubmed:year2006lld:pubmed
pubmed-article:16271741pubmed:articleTitleSelective elimination of HIV-1-infected cells by Env-directed, HIV-1-based virus-like particles.lld:pubmed
pubmed-article:16271741pubmed:affiliationAIDS Center, Istituto Superiore di Sanità, Viale Regina Elena, 299, 00161 Rome, Italy.lld:pubmed
pubmed-article:16271741pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:16271741pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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