| Literature DB >> 25253665 |
Sharon E Frey1, Laurence Peiperl2, M Juliana McElrath3, Spyros Kalams4, Paul A Goepfert5, Michael C Keefer6, Lindsey R Baden7, Michelle A Lally8, Kenneth Mayer9, William A Blattner10, Clayton D Harro11, Scott M Hammer12, Geoffrey J Gorse13, John Hural14, Georgia D Tomaras15, Yves Levy16, Peter Gilbert17, Allan deCamp17, Nina D Russell18, Marnie Elizaga14, Mary Allen19, Lawrence Corey3.
Abstract
Finding an effective human immunodeficiency virus type 1 (HIV-1) vaccine remains a major global health priority. In a phase I/II, placebo-controlled trial, healthy, HIV-1-negative adults were randomized to receive one of 5 vaccine regimens: LIPO-5 (combination of 5 lipopeptides) alone (250 μg), ALVAC-HIV (vCP1452) alone, or 3 groups of ALVAC-HIV (vCP1452) followed by ALVAC-HIV (vCP1452) plus LIPO-5 (250, 750, and 2,500 μg). Only 73/174 participants (42%) received all four vaccinations due to a study halt related to myelitis. There were no significant differences in systemic reactions between groups or in local reactogenicity between groups receiving ALVAC-HIV (vCP1452). Significant differences in local reactogenicity occurred between groups receiving LIPO-5 (P ≤ 0.05). Gag and Env antibodies were undetectable by ELISA 2 weeks after the fourth vaccination for all but one recipient. Antibodies to Gag and Env were present in 32% and 24% of recipients of ALVAC-HIV (vCP1452) alone and in 47% and 35% of ALVAC-HIV (vCP1452)+LIPO recipients, respectively. Coadministration of LIPO-5 did not significantly increase the response rate compared to ALVAC-HIV (vCP1452) alone, nor was there a significant relationship between dose and antibody responses among ALVAC-HIV (vCP1452)+LIPO groups. Over 90% of study participants had no positive gamma interferon (IFN-γ) enzyme-linked immunosorbent spot assay (ELISpot) responses to any peptide pool at any time point. The study was halted due to a case of myelitis possibly related to the LIPO-5 vaccine; this case of myelitis remains an isolated event. In general, there was no appreciable cell-mediated immunity detected in response to the vaccines used in this study, and antibody responses were limited. The clinical trial is registered on ClinicalTrials.gov with registry number NCT00076063.Entities:
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Year: 2014 PMID: 25253665 PMCID: PMC4248765 DOI: 10.1128/CVI.00450-14
Source DB: PubMed Journal: Clin Vaccine Immunol ISSN: 1556-679X