Ouzama NicholsonFay DicandiloJames KublinXiao SunErin QuirkMichelle MillerGlenda GrayJean PapeMichael N. RobertsonDevan V. MehrotraSteven SelfKatherine TurnerJorge SanchezPunnee PitisuttithumAnn DuerrSheri DubeyLisa KiersteadDanilo CasimiroScott M. HammerMerck & Co., Inc.GlaxoSmithKline, USAFred Hutchinson Cancer Research CenterUniversity of WitwatersrandWeill Cornell Medical CollegeAsociación Civil Impacta Salud y EducaciónInvestigaciones Medicas en SaludMahidol UniversityUniversity of Washington, SeattleColumbia University in the City of New York2018-05-032018-05-032011-05-01AIDS Research and Human Retroviruses. Vol.27, No.5 (2011), 557-567088922292-s2.0-79955774295https://repository.li.mahidol.ac.th/handle/20.500.14594/12056The 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 × 10 9 or 1 × 10 10 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/10 6 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/10 6 PBMCs in the placebo, 1 × 10 9 vp/dose, and 1 × 10 10 vp/dose groups, respectively. Overall, responses to 1 × 10 10 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 × 10 10 vp/dose groups than in the 1 × 10 9 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. © Copyright 2011, Mary Ann Liebert, Inc.Mahidol UniversityImmunology and MicrobiologyMedicineArticleSCOPUS10.1089/aid.2010.0151