| Literature DB >> 14741168 |
David Davis1, Helen Donners, Betty Willems, Karin Lövgren-Bengtsson, Lennart Akerblom, Guido Vanham, Susan Barnett, Bror Morein, Jonathan L Heeney, Guido van der Groen.
Abstract
Phase III efficacy trials of recombinant human immunodeficiency virus type 1 (HIV-1) envelope glycoproteins were postponed. In Phase I and II trials these candidate vaccines had failed to induce neutralizing antibodies against virus which had been isolated by co-culture with human peripheral blood mononuclear cells (PBMC). The aim of the present study was to determine assay conditions for detecting neutralization of primary HIV-1 isolates with sera from immunized individuals. We show that in two immunogenicity trials in rhesus macaques, recombinant HIV-1 SF2 gp120 induced antibodies which neutralized the primary HIV-1 SF13 isolate. Statistically significant in vitro neutralization required assays in which the incubation phase was extended. Sterile immunity was only seen with the highest level of neutralization, induced by a recombinant prime, peptide boost strategy. We recommend that neutralization assays with extended incubation phases should be used to monitor Phase III efficacy trials.Entities:
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Year: 2004 PMID: 14741168 DOI: 10.1016/j.vaccine.2003.08.031
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641