<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(1)</volume><submitter>Khan S</submitter><funding>Janssen Vaccines &amp;amp; Prevention, Leiden, Netherlands</funding><pubmed_abstract>The adenovirus (Ad)26 serotype-based vector vaccine Ad26.COV2.S has been used in millions of subjects for the prevention of COVID-19, but potentially elicits persistent anti-vector immunity. We investigated if vaccine-elicited immunity to Ad26 vector-based vaccines significantly influences antigen-specific immune responses induced by a subsequent vaccination with Ad26 vector-based vaccine regimens against different disease targets in non-human primates. A homologous Ad26 vector-based vaccination regimen or heterologous regimens (Ad26/Ad35 or Ad26/Modified Vaccinia Ankara [MVA]) induced target pathogen-specific immunity in animals, but also persistent neutralizing antibodies and T-cell responses against the vectors. However, subsequent vaccination (interval, 26-57 weeks) with homologous and</pubmed_abstract><journal>NPJ vaccines</journal><pagination>146</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9664441</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Sequential use of Ad26-based vaccine regimens in NHP to induce immunity against different disease targets.</pubmed_title><pmcid>PMC9664441</pmcid><pubmed_authors>Serroyen J</pubmed_authors><pubmed_authors>Schuitemaker H</pubmed_authors><pubmed_authors>Salisch NC</pubmed_authors><pubmed_authors>Zahn RC</pubmed_authors><pubmed_authors>Boer KF</pubmed_authors><pubmed_authors>Boedhoe S</pubmed_authors><pubmed_authors>Khan S</pubmed_authors><pubmed_authors>Gil AI</pubmed_authors></additional><is_claimable>false</is_claimable><name>Sequential use of Ad26-based vaccine regimens in NHP to induce immunity against different disease targets.</name><description>The adenovirus (Ad)26 serotype-based vector vaccine Ad26.COV2.S has been used in millions of subjects for the prevention of COVID-19, but potentially elicits persistent anti-vector immunity. We investigated if vaccine-elicited immunity to Ad26 vector-based vaccines significantly influences antigen-specific immune responses induced by a subsequent vaccination with Ad26 vector-based vaccine regimens against different disease targets in non-human primates. A homologous Ad26 vector-based vaccination regimen or heterologous regimens (Ad26/Ad35 or Ad26/Modified Vaccinia Ankara [MVA]) induced target pathogen-specific immunity in animals, but also persistent neutralizing antibodies and T-cell responses against the vectors. However, subsequent vaccination (interval, 26-57 weeks) with homologous and</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-05T15:41:08.789Z</modification><creation>2024-10-15T07:17:41.539Z</creation></dates><accession>S-EPMC9664441</accession><cross_references><pubmed>36379957</pubmed><doi>10.1038/s41541-022-00567-w</doi></cross_references></HashMap>