| Literature DB >> 29788316 |
Charles W Dobard1, Natalia Makarova1, Rolieria West-Deadwyler1, Andrew Taylor2, Chuong Dinh1, Amy Martin1, Jonathan Lipscomb1, James Mitchell1, George Khalil1, Gerardo Garcia-Lerma1, Walid Heneine1.
Abstract
Vaginal microbicides containing antiretrovirals (ARVs) have shown to prevent vaginally acquired human immunodeficiency virus (HIV), but these products may not protect women who engage in anal sex. Intravaginal dosing with ARVs has shown to result in drug exposures in rectal tissues, thus raising the possibility of dual compartment protection. To test this concept, we investigated whether intravaginal dosing with emtricitabine (FTC)/tenofovir (TFV) gel, which fully protected macaques against repeated vaginal exposures to simian human immunodeficiency virus (SHIV), protects against rectal SHIV exposures. Pharmacokinetic studies revealed rapid distribution of FTC and TFV to rectal tissues and luminal fluids, albeit at concentrations 1-2 log10 lower than those in the vaginal compartment. Efficacy measurements against repeated rectal SHIV challenges demonstrated a 4.5-fold reduction in risk of infection in macaques that received intravaginal FTC/TFV compared to placebo gel (P = .047; log-rank test). These data support the concept of dual compartment protection by vaginal dosing and warrants developing ARV-based vaginal products with improved bidirectional dosing.Entities:
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Year: 2018 PMID: 29788316 PMCID: PMC6129108 DOI: 10.1093/infdis/jiy301
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226