<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mdluli T</submitter><funding>NIAID NIH HHS</funding><pagination>114344</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11298786</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>43(6)</volume><pubmed_abstract>A heterologous Ad26/MVA vaccine was given prior to an analytic treatment interruption (ATI) in people living with HIV-1 (mainly CRF01_AE) who initiated antiretroviral treatment (ART) during acute HIV-1. We investigate the impact of Ad26/MVA vaccination on antibody (Ab)-mediated immune responses and their effect on time to viral rebound. The vaccine mainly triggers vaccine-matched binding Abs while, upon viral rebound post ATI, infection-specific CRF01_AE binding Abs increase in all participants. Binding Abs are not associated with time to viral rebound. The Ad26/MVA mosaic vaccine profile consists of correlated non-CRF01_AE binding Ab and Fc effector features, with strong Ab-dependent cellular phagocytosis (ADCP) responses. CRF01_AE-specific ADCP responses (measured either prior to or post</pubmed_abstract><journal>Cell reports</journal><pubmed_title>Mosaic vaccine-induced antibody-dependent cellular phagocytosis associated with delayed HIV-1 viral load rebound post treatment interruption.</pubmed_title><pmcid>PMC11298786</pmcid><funding_grant_id>UM1 AI126603</funding_grant_id><pubmed_authors>Kroon E</pubmed_authors><pubmed_authors>Pinyakorn S</pubmed_authors><pubmed_authors>Rolland M</pubmed_authors><pubmed_authors>Phanupak N</pubmed_authors><pubmed_authors>Vasan S</pubmed_authors><pubmed_authors>Tran U</pubmed_authors><pubmed_authors>Schuitemaker H</pubmed_authors><pubmed_authors>Hsu DC</pubmed_authors><pubmed_authors>Trautmann L</pubmed_authors><pubmed_authors>Dussupt V</pubmed_authors><pubmed_authors>Stieh DJ</pubmed_authors><pubmed_authors>Slike BM</pubmed_authors><pubmed_authors>de Souza M</pubmed_authors><pubmed_authors>Ake JA</pubmed_authors><pubmed_authors>Colby DJ</pubmed_authors><pubmed_authors>Ananworanich J</pubmed_authors><pubmed_authors>Pau MG</pubmed_authors><pubmed_authors>Shubin Z</pubmed_authors><pubmed_authors>Mdluli T</pubmed_authors><pubmed_authors>Mendez-Rivera L</pubmed_authors><pubmed_authors>Sacdalan C</pubmed_authors><pubmed_authors>Curtis DJ</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Tomaka FL</pubmed_authors><pubmed_authors>Robb ML</pubmed_authors><pubmed_authors>Krebs SJ</pubmed_authors><pubmed_authors>Paquin-Proulx D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Mosaic vaccine-induced antibody-dependent cellular phagocytosis associated with delayed HIV-1 viral load rebound post treatment interruption.</name><description>A heterologous Ad26/MVA vaccine was given prior to an analytic treatment interruption (ATI) in people living with HIV-1 (mainly CRF01_AE) who initiated antiretroviral treatment (ART) during acute HIV-1. We investigate the impact of Ad26/MVA vaccination on antibody (Ab)-mediated immune responses and their effect on time to viral rebound. The vaccine mainly triggers vaccine-matched binding Abs while, upon viral rebound post ATI, infection-specific CRF01_AE binding Abs increase in all participants. Binding Abs are not associated with time to viral rebound. The Ad26/MVA mosaic vaccine profile consists of correlated non-CRF01_AE binding Ab and Fc effector features, with strong Ab-dependent cellular phagocytosis (ADCP) responses. CRF01_AE-specific ADCP responses (measured either prior to or post</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jun</publication><modification>2026-06-01T15:24:59.777Z</modification><creation>2025-02-19T04:40:53.562Z</creation></dates><accession>S-EPMC11298786</accession><cross_references><pubmed>38850529</pubmed><doi>10.1016/j.celrep.2024.114344</doi></cross_references></HashMap>