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. 2011 May;27(5):557-567.
doi: 10.1089/AID.2010.0151. Epub 2010 Nov 23.

Safety and Immunogenicity of the MRKAd5 gag HIV Type 1 Vaccine in a Worldwide Phase 1 Study of Healthy Adults

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Safety and Immunogenicity of the MRKAd5 gag HIV Type 1 Vaccine in a Worldwide Phase 1 Study of Healthy Adults

Ouzama Nicholson et al. AIDS Res Hum Retroviruses. 2011 May.

Abstract

The safety and immunogenicity of the MRK adenovirus type 5 (Ad5) HIV-1 clade B gag vaccine was assessed in an international Phase I trial. Three-hundred and sixty healthy HIV-uninfected adults were enrolled on five continents. Subjects received placebo or 1 × 109 or 1 × 1010 viral particles (vp) per dose of the MRKAd5 HIV-1 gag vaccine at day 1, week 4, and week 26. Immunogenicity was evaluated using an IFN-γ ELISPOT gag 15-mer assay with positive responses defined as ≥55 SFC/106 PBMCs and ≥4-fold over mock control. The vaccine was well tolerated. The most common adverse events were injection site reactions, headache, pyrexia, diarrhea, fatigue, and myalgia. At week 30, geometric mean ELISPOT responses were 24, 114, and 226 SFC/106 PBMCs in the placebo, 1 × 109 vp/dose, and 1 × 1010 vp/dose groups, respectively. Overall, responses to 1 × 1010 vp were 85% and 68% in subjects with low (≤200) and high (>200) baseline Ad5 titers, respectively. The MRKAd5 HIV-1 gag vaccine was immunogenic in diverse geographic regions. Gag ELISPOT responses were greater in the 1 × 1010 vp/dose groups than in the 1 × 109 vp/dose groups. Data from this first international study indicate that adenovirus-vectored vaccines are well tolerated and may be immunogenic in subjects from regions with high prevalence of preexisting Ad5 immunity.

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Figures

FIG. 1.
FIG. 1.
Subject accounting. A total of 32 vaccinated subjects (30 in the vaccine groups and two in the placebo group) were excluded from the primary immunogenicity analysis. Reasons for exclusion are provided.
FIG. 2.
FIG. 2.
MRKAd5 gag ELISPOT response (SFC/106 PBMC) versus baseline anti-Ad5 antibody titer by dose level (all regions pooled). The figure demonstrates a significant decline in ELISPOT with increasing Ad5 titer at the 1 × 109 dose, but not at the 1 × 1010 dose. Filled circles (•) indicate participants who were ELISPOT positive or seroresponders. Open circles (○) indicate participants who were ELISPOT negative or nonresponders.
FIG. 3.
FIG. 3.
Gag ELISPOT response over time by dose level and baseline anti-Ad5 antibody strata (all regions pooled): critical time points only with confidence intervals. Antibody titers persisted through week 78 at levels near that achieved at week 30.

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