Protection by Vaccines and Previous Infection Against the Omicron Variant of Severe Acute Respiratory Syndrome Coronavirus 2
- PMID: 35482442
- PMCID: PMC9129207
- DOI: 10.1093/infdis/jiac161
Protection by Vaccines and Previous Infection Against the Omicron Variant of Severe Acute Respiratory Syndrome Coronavirus 2
Erratum in
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Correction to: "Protection by Vaccines and Previous Infection Against the Omicron Variant of Severe Acute Respiratory Syndrome Coronavirus 2".J Infect Dis. 2023 Apr 18;227(8):1021-1022. doi: 10.1093/infdis/jiac429. J Infect Dis. 2023. PMID: 36477265 Free PMC article. No abstract available.
Abstract
Background: The Omicron variant of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) evades immunity conferred by vaccines and previous infections.
Methods: We used a Cox proportional hazards model and a logistic regression on individual-level population-wide data from the Czech Republic to estimate risks of infection and hospitalization, including severe states.
Results: A recent (≤2 months) full vaccination reached vaccine effectiveness (VE) of 43% (95% confidence interval [CI], 42%-44%) against infection by Omicron compared to 73% (95% CI, 72%-74%) against Delta. A recent booster increased VE to 56% (95% CI, 55%-56%) against Omicron infection compared to 90% (95% CI, 90%-91%) for Delta. The VE against Omicron hospitalization of a recent full vaccination was 45% (95% 95% CI, 29%-57%), with a recent booster 87% (95% CI, 84%-88%). The VE against the need for oxygen therapy due to Omicron was 57% (95% CI, 32%-72%) for recent vaccination, 90% (95% CI, 87%-92%) for a recent booster. Postinfection protection against Omicron hospitalization declined from 68% (95% CI, 68%-69%) at ≤6 months to 13% (95% CI, 11%-14%) at >6 months after a previous infection. The odds ratios for Omicron relative to Delta were 0.36 (95% CI, .34-.38) for hospitalization, 0.24 (95% CI, .22-.26) for oxygen, and 0.24 (95% CI, .21-.28) for intensive care unit admission.
Conclusions: Recent vaccination still brings substantial protection against severe outcome for Omicron.
Keywords: COVID-19; Omicron variant; SARS-CoV-2; hospitalization; postinfection immunity; vaccine effectiveness.
© The Author(s) 2022. Published by Oxford University Press on behalf of Infectious Diseases Society of America. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
Conflict of interest statement
Potential conflicts of interest. The authors: No reported conflicts of interest. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.
Comment in
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Protection Against Severe Clinical Outcomes With Adenovirus or Messenger RNA Severe Acute Respiratory Syndrome Coronavirus 2 Vaccines in Patients Hospitalized With Coronavirus Disease 2019.J Infect Dis. 2022 Sep 13;226(5):938-940. doi: 10.1093/infdis/jiac256. J Infect Dis. 2022. PMID: 35763360 Free PMC article. No abstract available.
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Reply to Llibre et al.J Infect Dis. 2022 Sep 13;226(5):941. doi: 10.1093/infdis/jiac258. J Infect Dis. 2022. PMID: 35763365 No abstract available.
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More Analyses are Needed to Evaluate the Effectiveness of Protection by Vaccines and Previous Infection Against the Omicron Variant of SARS-CoV-2.J Infect Dis. 2022 Sep 13;226(5):942-943. doi: 10.1093/infdis/jiac257. J Infect Dis. 2022. PMID: 35763367 Free PMC article. No abstract available.
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Response to Beran et al.J Infect Dis. 2022 Sep 13;226(5):944-945. doi: 10.1093/infdis/jiac259. J Infect Dis. 2022. PMID: 35763416 No abstract available.
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