<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mayer-Blackwell K</submitter><funding>National Institute of Allergy and Infectious Diseases</funding><funding>NIAID NIH HHS</funding><funding>Center for AIDS Research, Duke University</funding><pagination>983313</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9597301</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13</volume><pubmed_abstract>Many participants in HIV-1 vaccine trials, who have not previously been exposed to or vaccinated against HIV-1, display serum immunoglobulin antibodies that bind the gp41 region of HIV-1 envelope prior to vaccination. Previous studies have hypothesized that these pre-existing antibodies may be cross-reactive and may skew future vaccine responses. In 12 large studies conducted by the HIV Vaccine Trial Network (HVTN) (n=1470 individuals), we find wide variation among participants in the pre-vaccine levels of gp41-reactive antibodies as measured by the binding antibody multiplex assay (BAMA). In the absence of exposure to the gp41 immunogen, anti-gp41 IgG levels were temporally stable over 26-52 weeks in repeated measures of placebo recipients. The analysis revealed that the geometric mean of</pubmed_abstract><journal>Frontiers in immunology</journal><pubmed_title>Multi-trial analysis of HIV-1 envelope gp41-reactive antibodies among global recipients of candidate HIV-1 vaccines.</pubmed_title><pmcid>PMC9597301</pmcid><funding_grant_id>U01 AI068614</funding_grant_id><funding_grant_id>U01 AI068635</funding_grant_id><funding_grant_id>UM1 AI068635</funding_grant_id><funding_grant_id>U01 AI068618</funding_grant_id><funding_grant_id>UM1 AI068614</funding_grant_id><funding_grant_id>P30 AI064518</funding_grant_id><funding_grant_id>UM1 AI068618</funding_grant_id><funding_grant_id>AI068618, AI068635, AI068614</funding_grant_id><pubmed_authors>Potchen N</pubmed_authors><pubmed_authors>Heptinstall J</pubmed_authors><pubmed_authors>Minot SS</pubmed_authors><pubmed_authors>Sawant S</pubmed_authors><pubmed_authors>Mayer-Blackwell K</pubmed_authors><pubmed_authors>Kublin JG</pubmed_authors><pubmed_authors>Seaton K</pubmed_authors><pubmed_authors>Shen X</pubmed_authors><pubmed_authors>Tomaras GD</pubmed_authors><pubmed_authors>Johnson AM</pubmed_authors><pubmed_authors>Fiore-Gartland A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Multi-trial analysis of HIV-1 envelope gp41-reactive antibodies among global recipients of candidate HIV-1 vaccines.</name><description>Many participants in HIV-1 vaccine trials, who have not previously been exposed to or vaccinated against HIV-1, display serum immunoglobulin antibodies that bind the gp41 region of HIV-1 envelope prior to vaccination. Previous studies have hypothesized that these pre-existing antibodies may be cross-reactive and may skew future vaccine responses. In 12 large studies conducted by the HIV Vaccine Trial Network (HVTN) (n=1470 individuals), we find wide variation among participants in the pre-vaccine levels of gp41-reactive antibodies as measured by the binding antibody multiplex assay (BAMA). In the absence of exposure to the gp41 immunogen, anti-gp41 IgG levels were temporally stable over 26-52 weeks in repeated measures of placebo recipients. The analysis revealed that the geometric mean of</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-06-01T02:25:32.8Z</modification><creation>2025-04-04T09:42:29.126Z</creation></dates><accession>S-EPMC9597301</accession><cross_references><pubmed>36311720</pubmed><doi>10.3389/fimmu.2022.983313</doi></cross_references></HashMap>