Literature DB >> 22814162

Double oral administration of emtricitabine/tenofovir prior to virus exposure protects against highly pathogenic simian/human immunodeficiency virus infection in macaques.

Tadashi Nakasone1, Tsutomu Murakami, Naoki Yamamoto.   

Abstract

In the absence of any effective vaccine against human immunodeficiency virus (HIV), current anti-retroviral drugs may be suitable for pre-exposure prophylaxis (PrEP). Previous large clinical trials showed that PrEP reduced HIV infection in high-risk populations. Emtricitabine/tenofovir (FTC/TDF) may be a suitable agent for PrEP. FTC/TDF PrEP efficacy was evaluated using a highly pathogenic simian/human immunodeficiency virus (SHIV) in a non-human primate model of AIDS, the SHIV-KS661c/cynomolgus monkey model. Double oral administration of FTC/TDF (20/30 mg/kg), at 24 h and a few minutes prior to exposure, completely protected 2/3 monkeys from infection. Interestingly, a single oral administration 2 weeks before viral exposure moderately rescued CD4 cells, although the data did not reach statistical significance. These results are consistent with previous primate studies and with recent clinical data.

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Year:  2012        PMID: 22814162     DOI: 10.7883/yoken.65.345

Source DB:  PubMed          Journal:  Jpn J Infect Dis        ISSN: 1344-6304            Impact factor:   1.362


  2 in total

1.  Single oral administration of the novel CXCR4 antagonist, KRH-3955, induces an efficient and long-lasting increase of white blood cell count in normal macaques, and prevents CD4 depletion in SHIV-infected macaques: a preliminary study.

Authors:  Tadashi Nakasone; Sei Kumakura; Michiko Yamamoto; Tsutomu Murakami; Naoki Yamamoto
Journal:  Med Microbiol Immunol       Date:  2012-07-08       Impact factor: 3.402

Review 2.  Animal models for microbicide safety and efficacy testing.

Authors:  Ronald S Veazey
Journal:  Curr Opin HIV AIDS       Date:  2013-07       Impact factor: 4.283

  2 in total

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