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In vitro and in vivo evaluation of two carrageenan-based formulations to prevent HPV acquisition.

Authors :
Rodríguez A
Kleinbeck K
Mizenina O
Kizima L
Levendosky K
Jean-Pierre N
Villegas G
Ford BE
Cooney ML
Teleshova N
Robbiani M
Herold BC
Zydowsky T
Fernández Romero JA
Source :
Antiviral research [Antiviral Res] 2014 Aug; Vol. 108, pp. 88-93. Date of Electronic Publication: 2014 Jun 05.
Publication Year :
2014

Abstract

Commercial vaccines against human papillomavirus (HPV) have low uptake due to parental autonomy, dosing regimen, cost, and cold chain storage requirements. Carrageenan (CG)-based formulations prevent HPV infection in vitro and in vivo but data are needed on the durability of anti-HPV activity and the effect of seminal plasma (SP). The Population Council's PC-515 gel and the lubricant Divine 9 were tested for their physicochemical properties and anti-HPV activity against HPV16, 18, and 45 pseudoviruses (PsVs). Anti-PsV activity was estimated using the luciferase assay in HeLa cells and the HPV PsV luciferase mouse model. Formulations were applied intravaginally either 2h pre/2h post (-2h/+2h) or 24h pre (-24h) relative to challenge with HPV16 or 45 PsV in PBS or SP/PBS. Both formulations showed broad-spectrum anti-HPV activity in vitro (IC50: 1-20ng/ml), significantly decreasing HPV PsV infection in the mouse model (-2h/+2h, p<0.0001). PC-515 protected better than Divine 9 in the -24h dosing regimen (p<0.0001) and comparable to Divine 9 in the -2h/+2h regimen (p=0.9841). PC-515 retained full activity in the murine model when PsV solutions contained human SP. The durable, potential broad-spectrum anti-HPV activity of CG formulations in the presence of SP supports their further development to prevent HPV acquisition.<br /> (Copyright © 2014 The Authors. Published by Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1872-9096
Volume :
108
Database :
MEDLINE
Journal :
Antiviral research
Publication Type :
Academic Journal
Accession number :
24909570
Full Text :
https://doi.org/10.1016/j.antiviral.2014.05.018