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Evaluation of ODE‐Bn‐PMEG, an acyclic nucleoside phosphonate prodrug, as an antiviral against productive HPV infection in 3D organotypic epithelial cultures

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HighlightsODE‐Bn‐PMEG abolishes human papillomavirus productive infection in 3D cultures of primary human keratinocytes (PHKs).Incorporation of activated ODE‐Bn‐PMEG into replicating DNA causes DNA breaks and abolishes viral activities.ODE‐Bn‐PMEG induces apoptosis selectively… Click to show full abstract

HighlightsODE‐Bn‐PMEG abolishes human papillomavirus productive infection in 3D cultures of primary human keratinocytes (PHKs).Incorporation of activated ODE‐Bn‐PMEG into replicating DNA causes DNA breaks and abolishes viral activities.ODE‐Bn‐PMEG induces apoptosis selectively in HPV‐infected, differentiated keratinocytes while sparing uninfected tissues.Cidofovir, which is used to treat human cytomegalovirus retinitis, neither induces apoptosis nor abolishes HPV activity.With its efficacy, selectivity and mechanism of action, ODE‐Bn‐PMEG strongly merits further development and clinical trials.

Keywords: acyclic nucleoside; ode pmeg; nucleoside phosphonate; infection; pmeg acyclic; evaluation ode

Journal Title: Antiviral Research
Year Published: 2018

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