<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>74(7)</volume><submitter>Skowronski DM</submitter><funding>Roche, Hologic, and Siemens</funding><funding>Public Health Agency of Canada</funding><funding>GlaxoSmithKline</funding><funding>Symvivo</funding><funding>Pfizer</funding><funding>BC Children’s Hospital Foundation</funding><funding>Michael Smith Foundation for Health Research</funding><funding>Sanofi-Pasteur</funding><funding>Seqirus</funding><funding>Canadian Institutes of Health Research</funding><funding>Merck</funding><funding>Canadian Child Health Clinician Scientist Program,</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>Randomized-controlled trials of messenger RNA (mRNA) vaccine protection against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) included relatively few elderly participants. We assess single-dose mRNA vaccine effectiveness (VE) in adults ≥ 70 years old in British Columbia, Canada, where second doses were deferred by up to 16 weeks and where a spring 2021 wave uniquely included codominant circulation of Alpha (B.1.1.7) and Gamma (P.1) variants of concern (VOC).&lt;h4>Methods&lt;/h4>Analyses included community-dwelling adults ≥ 70 years old with specimen collection between 4 April (epidemiological week 14) and 1 May (week 17) 2021. Adjusted VE was estimated by test-negative design. Cases were reverse-transcription polymerase chain reaction (RT-PCR) test-positive for</pubmed_abstract><journal>Clinical infectious diseases : an official publication of the Infectious Diseases Society of America</journal><pagination>1158-1165</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8406884</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Single-dose mRNA Vaccine Effectiveness Against Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), Including Alpha and Gamma Variants: A Test-negative Design in Adults 70 Years and Older in British Columbia, Canada.</pubmed_title><pmcid>PMC8406884</pmcid><pubmed_authors>Zou M</pubmed_authors><pubmed_authors>Patrick DM</pubmed_authors><pubmed_authors>Henry B</pubmed_authors><pubmed_authors>El Adam S</pubmed_authors><pubmed_authors>Skowronski DM</pubmed_authors><pubmed_authors>Jassem AN</pubmed_authors><pubmed_authors>Krajden M</pubmed_authors><pubmed_authors>Sadarangani M</pubmed_authors><pubmed_authors>Hoang LMN</pubmed_authors><pubmed_authors>Prystajecky N</pubmed_authors><pubmed_authors>Setayeshgar S</pubmed_authors><pubmed_authors>Naus M</pubmed_authors><pubmed_authors>Tyson JR</pubmed_authors><pubmed_authors>Sbihi H</pubmed_authors><pubmed_authors>Galanis E</pubmed_authors></additional><is_claimable>false</is_claimable><name>Single-dose mRNA Vaccine Effectiveness Against Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), Including Alpha and Gamma Variants: A Test-negative Design in Adults 70 Years and Older in British Columbia, Canada.</name><description>&lt;h4>Background&lt;/h4>Randomized-controlled trials of messenger RNA (mRNA) vaccine protection against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) included relatively few elderly participants. We assess single-dose mRNA vaccine effectiveness (VE) in adults ≥ 70 years old in British Columbia, Canada, where second doses were deferred by up to 16 weeks and where a spring 2021 wave uniquely included codominant circulation of Alpha (B.1.1.7) and Gamma (P.1) variants of concern (VOC).&lt;h4>Methods&lt;/h4>Analyses included community-dwelling adults ≥ 70 years old with specimen collection between 4 April (epidemiological week 14) and 1 May (week 17) 2021. Adjusted VE was estimated by test-negative design. Cases were reverse-transcription polymerase chain reaction (RT-PCR) test-positive for</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2026-05-08T22:53:27.552Z</modification><creation>2022-02-11T09:58:26.215Z</creation></dates><accession>S-EPMC8406884</accession><cross_references><pubmed>34244723</pubmed><doi>10.1093/cid/ciab616</doi></cross_references></HashMap>