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dc.contributor.authorBaeten, JM
dc.contributor.authorLingappa, J
dc.contributor.authorBeck, I
dc.contributor.authorFrenkel, LM
dc.contributor.authorPepper, G
dc.contributor.authorWald, A
dc.contributor.authorFife, KH
dc.contributor.authorWere, E
dc.contributor.authorMugo, N
dc.contributor.authorSanchez, J
dc.contributor.authorEssex, M
dc.contributor.authorMakhema, J
dc.contributor.authorKiarie, J
dc.contributor.authorFarquhar, C
dc.contributor.authorCorey, L
dc.date.accessioned2013-06-12T12:11:37Z
dc.date.available2013-06-12T12:11:37Z
dc.date.issued2011-01
dc.identifier.citationJ Infect Dis. 2011 Jan 1;203(1):117-21.en
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/21148504
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/32282
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC3024584/
dc.description.abstractRecent in vitro studies suggest that acyclovir may directly inhibit HIV-1 replication and can select for a specific HIV-1 reverse transcriptase mutation (V75I) with concomitant loss of an anti-HIV-1 effect. We tested for HIV-1 genotypic resistance at reverse transcriptase codon 75 in plasma from 168 HIV-1-infected persons from Botswana, Kenya, Peru, and the United States taking daily acyclovir or valacyclovir for between 8 weeks and 24 months. No V75I cases were detected (95% confidence interval, 0%-2.2%). These prospective in vivo studies suggest that standard-dose acyclovir or valacyclovir does not select for HIV-1 resistance.en
dc.language.isoenen
dc.publisherUnivesity of Nairobien
dc.titleHerpes simplex virus type 2 suppressive therapy with acyclovir or valacyclovir does not select for specific HIV-1 resistance in HIV-1/HSV-2 dually infected persons.en
dc.typeArticleen
local.publisherDepartment of Medicineen


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