<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Tan CS</submitter><funding>NICHD NIH HHS</funding><funding>NIAID NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>e2226335</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9366542</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>5(8)</volume><pubmed_abstract>&lt;h4>Importance&lt;/h4>Antibody responses elicited by current messenger RNA (mRNA) COVID-19 vaccines decline rapidly and require repeated boosting.&lt;h4>Objective&lt;/h4>To evaluate the immunogenicity and durability of heterologous and homologous prime-boost regimens involving the adenovirus vector vaccine Ad26.COV2.S and the mRNA vaccine BNT162b2.&lt;h4>Design, setting, and participants&lt;/h4>In this cohort study at a single clinical site in Boston, Massachusetts, 68 individuals who were vaccinated at least 6 months previously with 2 immunizations of BNT162b2 were boosted with either Ad26.COV2.S or BNT162b2. Enrollment of participants occurred from August 12, 2021, to October 25, 2021, and this study involved 4 months of follow-up. Data analysis was performed from November 2021 to February 2022.&lt;h4>Exp</pubmed_abstract><journal>JAMA network open</journal><pubmed_title>Durability of Heterologous and Homologous COVID-19 Vaccine Boosts.</pubmed_title><pmcid>PMC9366542</pmcid><funding_grant_id>T32 GM144273</funding_grant_id><funding_grant_id>T32 GM007753</funding_grant_id><funding_grant_id>K12 HD000849</funding_grant_id><funding_grant_id>T32 GM008313</funding_grant_id><funding_grant_id>F30 AI160908</funding_grant_id><funding_grant_id>R21 AI169309</funding_grant_id><pubmed_authors>McMahan K</pubmed_authors><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Roy V</pubmed_authors><pubmed_authors>Schmidt AG</pubmed_authors><pubmed_authors>Yu J</pubmed_authors><pubmed_authors>Hauser BM</pubmed_authors><pubmed_authors>Sadoff J</pubmed_authors><pubmed_authors>Tan CS</pubmed_authors><pubmed_authors>Alter G</pubmed_authors><pubmed_authors>Jacob-Dolan C</pubmed_authors><pubmed_authors>Meganck RM</pubmed_authors><pubmed_authors>Rowe M</pubmed_authors><pubmed_authors>Jaegle KH</pubmed_authors><pubmed_authors>Hemond R</pubmed_authors><pubmed_authors>Barouch DH</pubmed_authors><pubmed_authors>Munt JE</pubmed_authors><pubmed_authors>Powers JM</pubmed_authors><pubmed_authors>Le Gars M</pubmed_authors><pubmed_authors>Mallory ML</pubmed_authors><pubmed_authors>Mattocks M</pubmed_authors><pubmed_authors>Baric RS</pubmed_authors><pubmed_authors>He X</pubmed_authors><pubmed_authors>Bondzie EA</pubmed_authors><pubmed_authors>Collier AY</pubmed_authors><pubmed_authors>Chandrashekar A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Durability of Heterologous and Homologous COVID-19 Vaccine Boosts.</name><description>&lt;h4>Importance&lt;/h4>Antibody responses elicited by current messenger RNA (mRNA) COVID-19 vaccines decline rapidly and require repeated boosting.&lt;h4>Objective&lt;/h4>To evaluate the immunogenicity and durability of heterologous and homologous prime-boost regimens involving the adenovirus vector vaccine Ad26.COV2.S and the mRNA vaccine BNT162b2.&lt;h4>Design, setting, and participants&lt;/h4>In this cohort study at a single clinical site in Boston, Massachusetts, 68 individuals who were vaccinated at least 6 months previously with 2 immunizations of BNT162b2 were boosted with either Ad26.COV2.S or BNT162b2. Enrollment of participants occurred from August 12, 2021, to October 25, 2021, and this study involved 4 months of follow-up. Data analysis was performed from November 2021 to February 2022.&lt;h4>Exp</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2026-06-01T02:21:09.018Z</modification><creation>2025-04-19T05:56:37.109Z</creation></dates><accession>S-EPMC9366542</accession><cross_references><pubmed>35947380</pubmed><doi>10.1001/jamanetworkopen.2022.26335</doi></cross_references></HashMap>