<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ortiz JR</submitter><funding>NCATS NIH HHS</funding><funding>NIAID NIH HHS</funding><pagination>3253-3262</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9897630</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>40(23)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Influenza A/H7N9 viruses have pandemic potential.&lt;h4>Methods&lt;/h4>We conducted an open-label, randomized, controlled trial of AS03-adjuvanted 2017 inactivated influenza A/H7N9 vaccine (H7N9 IIV) in healthy adults. Group 1 received H7N9 IIV and seasonal quadrivalent influenza vaccine (IIV4) simultaneously, followed by H7N9 IIV three weeks later. Group 2 received IIV4 alone and then two doses of H7N9 IIV at three-week intervals. Group 3 received one dose of IIV4. We used hemagglutination inhibition (HAI) and microneutralization (MN) assays to measure geometric mean titers and seroprotection (≥1:40 titer) to vaccine strains and monitored for safety.&lt;h4>Results&lt;/h4>Among 149 subjects, seroprotection by HAI three weeks after H7N9 IIV dose 2 was 51% (95 %CI 37%-65%) for Group 1</pubmed_abstract><journal>Vaccine</journal><pubmed_title>Safety and immunogenicity of monovalent H7N9 influenza vaccine with AS03 adjuvant given sequentially or simultaneously with a seasonal influenza vaccine: A randomized clinical trial.</pubmed_title><pmcid>PMC9897630</pmcid><funding_grant_id>UM1 AI148372</funding_grant_id><funding_grant_id>HHSN272201300023I</funding_grant_id><funding_grant_id>UL1 TR003098</funding_grant_id><funding_grant_id>HHSN272201200003I</funding_grant_id><funding_grant_id>75N93021C00012</funding_grant_id><funding_grant_id>HHSN272201300016C</funding_grant_id><funding_grant_id>HHSN272201300023C</funding_grant_id><funding_grant_id>HHSN272201300016I</funding_grant_id><funding_grant_id>R01 AI145332</funding_grant_id><funding_grant_id>HHSN272200800057C</funding_grant_id><pubmed_authors>Neuzil KM</pubmed_authors><pubmed_authors>Ortiz JR</pubmed_authors><pubmed_authors>Overton ET</pubmed_authors><pubmed_authors>Wegel A</pubmed_authors><pubmed_authors>Goepfert PA</pubmed_authors><pubmed_authors>Cross K</pubmed_authors><pubmed_authors>Chen WH</pubmed_authors><pubmed_authors>Buddy Creech C</pubmed_authors><pubmed_authors>Logan HL</pubmed_authors><pubmed_authors>Parker S</pubmed_authors><pubmed_authors>Spearman PW</pubmed_authors><pubmed_authors>Dickey M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Safety and immunogenicity of monovalent H7N9 influenza vaccine with AS03 adjuvant given sequentially or simultaneously with a seasonal influenza vaccine: A randomized clinical trial.</name><description>&lt;h4>Background&lt;/h4>Influenza A/H7N9 viruses have pandemic potential.&lt;h4>Methods&lt;/h4>We conducted an open-label, randomized, controlled trial of AS03-adjuvanted 2017 inactivated influenza A/H7N9 vaccine (H7N9 IIV) in healthy adults. Group 1 received H7N9 IIV and seasonal quadrivalent influenza vaccine (IIV4) simultaneously, followed by H7N9 IIV three weeks later. Group 2 received IIV4 alone and then two doses of H7N9 IIV at three-week intervals. Group 3 received one dose of IIV4. We used hemagglutination inhibition (HAI) and microneutralization (MN) assays to measure geometric mean titers and seroprotection (≥1:40 titer) to vaccine strains and monitored for safety.&lt;h4>Results&lt;/h4>Among 149 subjects, seroprotection by HAI three weeks after H7N9 IIV dose 2 was 51% (95 %CI 37%-65%) for Group 1</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2026-05-28T19:00:44.545Z</modification><creation>2025-02-19T00:13:26.072Z</creation></dates><accession>S-EPMC9897630</accession><cross_references><pubmed>35465983</pubmed><doi>10.1016/j.vaccine.2022.03.055</doi></cross_references></HashMap>