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Protection against Omicron re-infection conferred by prior heterologous SARS-CoV-2 infection, with and without mRNA vaccination
Sara Carazo; Danuta M Skowronski; Marc Brisson; Chantal Sauvageau; Nicholas Brousseau; Rodica Gilca; Manale Ouakki; Sapha Barkati; Judith Fafard; Denis Talbot; Vladimir Gilca; Geneviève Deceuninck; Christophe Garenc; Alex Carignan; Philippe De Wals; Gaston De Serres.
Afiliação
  • Sara Carazo; Biological and occupational risks unit. Institut national de santé publique du Québec, Quebec city, Quebec, Canada
  • Danuta M Skowronski; BC Centre for Disease Control, Vancouver, British Columbia, Canada
  • Marc Brisson; Centre Hospitalier Universitaire (CHU) de Québec Université Laval Research Center, Quebec city, Quebec, Canada
  • Chantal Sauvageau; Biological and occupational risks unit. Institut national de santé publique du Québec, Quebec city, Quebec, Canada
  • Nicholas Brousseau; Biological and occupational risks unit. Institut national de santé publique du Québec, Quebec city, Quebec, Canada
  • Rodica Gilca; Biological and occupational risks unit. Institut national de santé publique du Québec, Quebec city, Quebec, Canada
  • Manale Ouakki; Biological and occupational risks unit. Institut national de santé publique du Québec, Quebec city, Quebec, Canada
  • Sapha Barkati; Department of Medicine, Division of infectious diseases, McGill University Health Center, McGill University, Montreal, Quebec, Canada
  • Judith Fafard; Laboratoire de Santé Publique du Québec, Institut national de santé publique du Québec, Sainte-Anne-de-Bellevue, Quebec, Canada
  • Denis Talbot; Centre Hospitalier Universitaire (CHU) de Québec Université Laval Research Center, Quebec city, Quebec, Canada
  • Vladimir Gilca; Biological and occupational risks unit. Institut national de santé publique du Québec, Quebec city, Quebec, Canada
  • Geneviève Deceuninck; Centre Hospitalier Universitaire (CHU) de Québec Université Laval Research Center, Quebec city, Quebec, Canada
  • Christophe Garenc; Biological and occupational risks unit. Institut national de santé publique du Québec, Quebec city, Quebec, Canada
  • Alex Carignan; Department of microbiology and infectious diseases, Sherbrook University, Sherbrook, Quebec, Canada
  • Philippe De Wals; Biological and occupational risks unit. Institut national de santé publique du Québec, Quebec city, Quebec, Canada
  • Gaston De Serres; Biological and occupational risks unit. Institut national de santé publique du Québec, Quebec city, Quebec, Canada
Preprint em Inglês | medRxiv | ID: ppmedrxiv-22274455
ABSTRACT
ImportanceOmicron is phylogenetically- and antigenically-distinct from earlier SARS-CoV-2 variants and the original vaccine strain. Protection conferred by prior SARS-CoV-2 infection against Omicron re-infection, and the added value of vaccination, require quantification. ObjectiveTo estimate protection against Omicron re-infection and hospitalization conferred by prior heterologous SARS-CoV-2 (non-Omicron) infection and/or up to three doses of (ancestral, Wuhan-like) mRNA vaccine. DesignTest-negative study between December 26 (epi-week 52), 2021 and March 12 (epi-week 10), 2022. SettingPopulation-based, province of Quebec, Canada ParticipantsCommunity-dwelling [≥]12-year-olds tested for SARS-CoV-2. ExposuresPrior laboratory-confirmed infection with/without mRNA vaccination. OutcomesLaboratory-confirmed SARS-CoV-2 re-infection and hospitalization, presumed Omicron by genomic surveillance. The odds of prior non-Omicron infection with/without vaccination were compared among Omicron cases/hospitalizations versus test-negative controls (single randomly-selected per individual). Adjusted odds ratios controlled for age, sex, testing-indication and epi-week. Analyses were stratified by severity and time since last non-Omicron infection or vaccine dose. ResultsWithout vaccination, prior non-Omicron infection reduced the Omicron re-infection risk by 44% (95%CI38-48), decreasing from 66% (95%CI57-73) at 3-5 months to 35% (95%CI21-47) at 9-11 months post-infection and <30% thereafter. The more severe the prior infection, the greater the risk reduction 8% (95%CI17-28), 43% (95%CI37-49) and 68% (95%CI51-80) for prior asymptomatic, symptomatic ambulatory or hospitalized infections. mRNA vaccine effectiveness against Omicron infection was consistently significantly higher among previously-infected vs. non-infected individuals at 65% (95%CI63-67) vs. 20% (95%CI16-24) for one-dose; 68% (95%CI67-70) vs. 42% (95%CI41-44) for two doses; and 83% (95%CI81-84) vs. 73% (95%CI72-73) for three doses. Infection-induced protection against Omicron hospitalization was 81% (95%CI 66-89) increasing to 86% (95%CI77-99) with one, 94% (95%CI91-96) with two and 97%(95%CI94-99) with three mRNA vaccine doses. Two-dose effectiveness against hospitalization among previously-infected individuals did not wane across 11 months and did not significantly differ from three-dose effectiveness despite longer follow-up (median 158 and 27 days, respectively). Conclusions and relevancePrior heterologous SARS-CoV-2 infection provided substantial and sustained protection against Omicron hospitalization, greatest among those also vaccinated. In the context of program goals to prevent severe outcomes and preserve healthcare system capacity, >2 doses of ancestral Wuhan-like vaccine may be of marginal incremental value to previously-infected individuals.
Licença
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Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Cohort_studies / Experimental_studies / Estudo observacional / Estudo prognóstico / Rct Idioma: Inglês Ano de publicação: 2022 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Cohort_studies / Experimental_studies / Estudo observacional / Estudo prognóstico / Rct Idioma: Inglês Ano de publicação: 2022 Tipo de documento: Preprint
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