| Literature DB >> 22265575 |
Carmen Sánchez-Jiménez1, Isabel Olivares, Ana Isabel de Ávila Lucas, Víctor Toledano, Mónica Gutiérrez-Rivas, Ramón Lorenzo-Redondo, Ana Grande-Pérez, Esteban Domingo, Cecilio López-Galíndez.
Abstract
Lethal mutagenesis, a new antiviral strategy to extinguish virus through elevated mutation rates, was explored in H61-D cells an HIV-1 persistently infected lymphoid cell line. Three mutagenic agents: 5-hydroxy-2(')-deoxycytidine (5-OHdC), 5-fluorouracil (5-FU) and 2,2(')-difluoro-2(')-deoxycytidine (gemcitabine) were used. After 54 passages, treatments with 5-FU and gemcitabine reduced virus infectivity, p24 and RT activity. Treatment with the pyrimidine analog 5-OHdC resulted in increases of p24 production, RT activity and infectivity. Rise in viral replication by 5-OHdC during HIV-1 persistence is in contrast with its inhibitory effect in acute infections. Viral replication enhancement by 5-OHdC was associated with an increase in intracellular HIV-1 RNA mutations. Mechanisms of HIV-1 replication enhancement by 5-OHdC are unknown but some potential factors are discussed. Increase of HIV-1 replication by 5-OHdC cautions against the use, without previous analyses, of mutagenic nucleoside analogs for AIDS treatment. Copyright ÂEntities:
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Year: 2012 PMID: 22265575 DOI: 10.1016/j.virol.2011.12.016
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616