<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Klingler J</submitter><funding>BLRD VA</funding><funding>NIAID NIH HHS</funding><funding>National Institutes of Health</funding><funding>U.S. Department of Veterans Affairs</funding><pagination>1382619</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11109367</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Antibodies against the SARS-CoV-2 spike protein are a critical immune determinant for protection against the virus. While virus neutralization is a key function of spike-specific antibodies, antibodies also mediate Fc-dependent activities that can play a role in protection or pathogenesis.&lt;h4>Methods&lt;/h4>This study characterized serum antibody responses elicited after two doses of heterologous adenovirus-vectored (Ad26/ Ad5) vaccines.&lt;h4>Results&lt;/h4>Vaccine-induced antibody binding titers and Fc-mediated functions decreased over six months, while neutralization titers remained stable. Comparison of antibody isotypes elicited after Ad26/Ad5 vs. LNP-mRNA vaccination and after infection showed that anti-spike IgG1 were dominant and produced to high levels in all groups. T</pubmed_abstract><journal>Frontiers in immunology</journal><pubmed_title>Heterologous Ad26/Ad5 adenovirus-vectored vaccines elicited SARS-CoV-2-specific antibody responses with potent Fc activities.</pubmed_title><pmcid>PMC11109367</pmcid><funding_grant_id>IK6 BX004607</funding_grant_id><funding_grant_id>HHSN272201400008C</funding_grant_id><funding_grant_id>75N93019C00051</funding_grant_id><funding_grant_id>R01 AI140909</funding_grant_id><funding_grant_id>R21 AI148033</funding_grant_id><funding_grant_id>R21 AI149033</funding_grant_id><funding_grant_id>U01 AI141990</funding_grant_id><funding_grant_id>U01 AI150747</funding_grant_id><funding_grant_id>R01 AI123449</funding_grant_id><funding_grant_id>I01 BX005794</funding_grant_id><funding_grant_id>R01 AI139290</funding_grant_id><funding_grant_id>AI139290, AI123449, AI1498033, 75N93019C00051, HHSN272201400008C, HHSN272201400006C, AI141990, AI150747, AI140909</funding_grant_id><funding_grant_id>I01BX005794, 1IK6BX004607</funding_grant_id><funding_grant_id>HHSN272201400006C</funding_grant_id><pubmed_authors>Emami-Gorizi R</pubmed_authors><pubmed_authors>Rao PG</pubmed_authors><pubmed_authors>Alvarez RA</pubmed_authors><pubmed_authors>Amanat F</pubmed_authors><pubmed_authors>Gleason C</pubmed_authors><pubmed_authors>Upadhyay C</pubmed_authors><pubmed_authors>Simon V</pubmed_authors><pubmed_authors>Kowdle S</pubmed_authors><pubmed_authors>Lee B</pubmed_authors><pubmed_authors>Klingler J</pubmed_authors><pubmed_authors>Perandones C</pubmed_authors><pubmed_authors>Hioe CE</pubmed_authors><pubmed_authors>Bandres JC</pubmed_authors><pubmed_authors>Kleiner G</pubmed_authors><pubmed_authors>Edelstein A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Heterologous Ad26/Ad5 adenovirus-vectored vaccines elicited SARS-CoV-2-specific antibody responses with potent Fc activities.</name><description>&lt;h4>Introduction&lt;/h4>Antibodies against the SARS-CoV-2 spike protein are a critical immune determinant for protection against the virus. While virus neutralization is a key function of spike-specific antibodies, antibodies also mediate Fc-dependent activities that can play a role in protection or pathogenesis.&lt;h4>Methods&lt;/h4>This study characterized serum antibody responses elicited after two doses of heterologous adenovirus-vectored (Ad26/ Ad5) vaccines.&lt;h4>Results&lt;/h4>Vaccine-induced antibody binding titers and Fc-mediated functions decreased over six months, while neutralization titers remained stable. Comparison of antibody isotypes elicited after Ad26/Ad5 vs. LNP-mRNA vaccination and after infection showed that anti-spike IgG1 were dominant and produced to high levels in all groups. T</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024</publication><modification>2026-04-12T19:09:43.355Z</modification><creation>2026-04-08T03:17:56.223Z</creation></dates><accession>S-EPMC11109367</accession><cross_references><pubmed>38779671</pubmed><doi>10.3389/fimmu.2024.1382619</doi></cross_references></HashMap>