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A single dose of a MIV-150/Zinc acetate gel provides 24 h of protection against vaginal simian human immunodeficiency virus reverse transcriptase infection, with more limited protection rectally 8-24 h after gel use.

Authors :
Kenney J
Singer R
Derby N
Aravantinou M
Abraham CJ
Menon R
Seidor S
Zhang S
Gettie A
Blanchard J
Piatak M Jr
Lifson JD
Fernández-Romero JA
Zydowsky TM
Robbiani M
Source :
AIDS research and human retroviruses [AIDS Res Hum Retroviruses] 2012 Nov; Vol. 28 (11), pp. 1476-84. Date of Electronic Publication: 2012 Jul 30.
Publication Year :
2012

Abstract

Previously we showed that repeated vaginal application of a MIV-150/zinc acetate carrageenan (MIV-150/ZA/CG) gel and a zinc acetate carrageenan (ZA/CG) gel significantly protected macaques from vaginal simian human immunodeficiency virus reverse transcriptase (SHIV-RT) infection. Gels were applied either daily for 2 weeks or every other day for 4 weeks, and the animals were challenged 4-24 h later. Herein, we examined the effects of a single vaginal dose administered either before or after virus challenge. Encouraged by the vaginal protection seen with MIV-150/ZA/CG, we also tested it rectally. Vaginal applications of MIV-150/ZA/CG, ZA/CG, and CG gel were performed once 8-24 h before, 1 h after, or 24 h before and 1 h after vaginal challenge. Rectal applications of MIV-150/ZA/CG and CG gel were performed once 8 or 24 h before rectal challenge. While vaginal pre-challenge and pre/post-challenge application of MIV-150/ZA/CG gel offered significant protection (88%, p<0.002), post-challenge application alone did not significantly protect. ZA/CG gel reduced infection prechallenge, but not significantly, and the effect was completely lost post-challenge. Rectal application of MIV-150/ZA/CG gel afforded limited protection against rectal challenge when applied 8-24 h before challenge. Thus, MIV-150/ZA/CG gel is a highly effective vaginal microbicide that demonstrates 24 h of protection from vaginal infection and may demonstrate efficacy against rectal infection when given close to the time of HIV exposure.

Details

Language :
English
ISSN :
1931-8405
Volume :
28
Issue :
11
Database :
MEDLINE
Journal :
AIDS research and human retroviruses
Publication Type :
Academic Journal
Accession number :
22737981
Full Text :
https://doi.org/10.1089/AID.2012.0087