Safety and immunogenicity of cytotoxic T-lymphocyte poly-epitope, DNA plasmid (EP HIV-1090) vaccine in healthy, human immunodeficiency virus type 1 (HIV-1)-uninfected adults

dc.contributor.authorNewman, M. J.
dc.contributor.authorGorse, G. J.
dc.contributor.authorBaden, L. R.
dc.contributor.authorWecker, M.
dc.contributor.authorNewman, M. J.
dc.contributor.authorFerrari, G.
dc.contributor.authorWeinhold, K. J.
dc.contributor.authorLivingston, B. D.
dc.contributor.authorVillafana, T. L.
dc.contributor.authorLi, H.
dc.contributor.authorNoonan, E.
dc.contributor.authorRussell, N. D.
dc.date.accessioned2012-04-30T14:38:21Z
dc.date.accessioned2017-10-19T12:08:03Z
dc.date.available2012-04-30T14:38:21Z
dc.date.available2017-10-19T12:08:03Z
dc.date.issued2008
dc.description.abstractWe evaluated EP HIV-1090 vaccine, a DNA plasmid encoding 21 cytotoxic T-lymphocyte (CTL) epitopes of human immunodeficiency virus type 1 (HIV-1) and the pan-DR helper T-lymphocyte epitope (PADRE), in a dose escalation, randomized, double-blinded, placebo-controlled Phase 1 trial. Vaccine, at 0.5, 2.0, or 4.0mg doses, or placebo was injected four times over 6 months. Forty-two healthy, HIV-1-uninfected adults were enrolled. Using an interferon-gamma ELISPOT assay, a response to PADRE was detected in one vaccine recipient. Three vaccine recipients raised anti-HIV-1 CD8+ CTL measured by chromium-release assay. The vaccine was safe and well-tolerated, but only weakly immunogenic.en_US
dc.identifier.urihttp://197.255.68.203/handle/123456789/846
dc.language.isoenen_US
dc.publisherVaccine Journal 26(2): 215-23en_US
dc.titleSafety and immunogenicity of cytotoxic T-lymphocyte poly-epitope, DNA plasmid (EP HIV-1090) vaccine in healthy, human immunodeficiency virus type 1 (HIV-1)-uninfected adultsen_US
dc.typeArticleen_US

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