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Effectiveness of Messenger RNA-based Vaccines During the Emergence of the Severe Acute Respiratory Syndrome Coronavirus 2 Omicron Variant.
Clin Infect Dis. 2022 Dec 19; 75(12):2186-2192.CI

Abstract

BACKGROUND

We evaluated the effectiveness of mRNA-based vaccines following emergence of SARS-CoV-2 Omicron variant.

METHODS

Recipients of a third dose of BNT162b2 or mRNA-1273 ≥180 days after the primary series were matched to primary-series recipients and unvaccinated persons. Participants were followed from 1 December 2021 to 12 March 2022. Outcomes were documented SARS-CoV-2 infection, COVID-19 hospitalization, and COVID-19 death. Effectiveness was calculated from 100-day risks estimated with the Kaplan-Meier estimator.

RESULTS

BNT162b2 and mRNA-1273 groups included 221 267 and 187 507 third-dose recipients, respectively, matched to equal numbers of primary-series recipients and unvaccinated persons. Compared with no vaccination, effectiveness of a third dose of BNT162b2 was 47.8% (95% confidence interval [CI], 45.2-50.3), 81.8% (95% CI, 79.2-84.2), and 89.6% (95% CI, 85.0-93.6) against infection, hospitalization, and death, respectively. Effectiveness of a third dose of BNT162b2 compared with the primary series was 30.1% (95% CI, 26.2-33.7), 61.4% (95% CI, 55.0-67.1), and 78.8% (95% CI, 67.9-87.5) against infection, hospitalization, and death, respectively. Effectiveness of a third dose of mRNA-1273 compared with no vaccination was 61.9% (95% CI, 59.4-64.4), 87.9% (95% CI, 85.3-90.2), and 91.4% (95% CI, 86.4-95.6) against infection, hospitalization, and death, respectively. Effectiveness of a third dose of mRNA-1273 compared with the primary series was 37.1% (95% CI, 32.2-41.7), 63.5% (95% CI, 53.7-71.6), and 75.0% (95% CI, 55.4-88.0) against infection, hospitalization, and death, respectively.

CONCLUSIONS

BNT162b2 and mRNA-1273 were effective against COVID-19 following emergence of Omicron variant. A third dose provided additional protection over the primary series.

Authors+Show Affiliations

Public Health Program, US Department of Veterans Affairs, Washington D.C., USA. Public Health Program, US Department of Veterans Affairs, Palo Alto, California, USA.Public Health Program, US Department of Veterans Affairs, Washington D.C., USA. Public Health Program, US Department of Veterans Affairs, Palo Alto, California, USA.Public Health Program, US Department of Veterans Affairs, Washington D.C., USA. Public Health Program, US Department of Veterans Affairs, Palo Alto, California, USA. Division of Infectious Disease & Geographic Medicine, Stanford University School of Medicine, Stanford, California, USA.

Pub Type(s)

Journal Article

Language

eng

PubMed ID

35475889

Citation

Sharma, Aditya, et al. "Effectiveness of Messenger RNA-based Vaccines During the Emergence of the Severe Acute Respiratory Syndrome Coronavirus 2 Omicron Variant." Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America, vol. 75, no. 12, 2022, pp. 2186-2192.
Sharma A, Oda G, Holodniy M. Effectiveness of Messenger RNA-based Vaccines During the Emergence of the Severe Acute Respiratory Syndrome Coronavirus 2 Omicron Variant. Clin Infect Dis. 2022;75(12):2186-2192.
Sharma, A., Oda, G., & Holodniy, M. (2022). Effectiveness of Messenger RNA-based Vaccines During the Emergence of the Severe Acute Respiratory Syndrome Coronavirus 2 Omicron Variant. Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America, 75(12), 2186-2192. https://doi.org/10.1093/cid/ciac325
Sharma A, Oda G, Holodniy M. Effectiveness of Messenger RNA-based Vaccines During the Emergence of the Severe Acute Respiratory Syndrome Coronavirus 2 Omicron Variant. Clin Infect Dis. 2022 Dec 19;75(12):2186-2192. PubMed PMID: 35475889.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Effectiveness of Messenger RNA-based Vaccines During the Emergence of the Severe Acute Respiratory Syndrome Coronavirus 2 Omicron Variant. AU - Sharma,Aditya, AU - Oda,Gina, AU - Holodniy,Mark, PY - 2022/2/7/received PY - 2022/4/28/pubmed PY - 2022/12/22/medline PY - 2022/4/27/entrez KW - COVID-19 KW - Omicron KW - epidemiology KW - vaccine SP - 2186 EP - 2192 JF - Clinical infectious diseases : an official publication of the Infectious Diseases Society of America JO - Clin Infect Dis VL - 75 IS - 12 N2 - BACKGROUND: We evaluated the effectiveness of mRNA-based vaccines following emergence of SARS-CoV-2 Omicron variant. METHODS: Recipients of a third dose of BNT162b2 or mRNA-1273 ≥180 days after the primary series were matched to primary-series recipients and unvaccinated persons. Participants were followed from 1 December 2021 to 12 March 2022. Outcomes were documented SARS-CoV-2 infection, COVID-19 hospitalization, and COVID-19 death. Effectiveness was calculated from 100-day risks estimated with the Kaplan-Meier estimator. RESULTS: BNT162b2 and mRNA-1273 groups included 221 267 and 187 507 third-dose recipients, respectively, matched to equal numbers of primary-series recipients and unvaccinated persons. Compared with no vaccination, effectiveness of a third dose of BNT162b2 was 47.8% (95% confidence interval [CI], 45.2-50.3), 81.8% (95% CI, 79.2-84.2), and 89.6% (95% CI, 85.0-93.6) against infection, hospitalization, and death, respectively. Effectiveness of a third dose of BNT162b2 compared with the primary series was 30.1% (95% CI, 26.2-33.7), 61.4% (95% CI, 55.0-67.1), and 78.8% (95% CI, 67.9-87.5) against infection, hospitalization, and death, respectively. Effectiveness of a third dose of mRNA-1273 compared with no vaccination was 61.9% (95% CI, 59.4-64.4), 87.9% (95% CI, 85.3-90.2), and 91.4% (95% CI, 86.4-95.6) against infection, hospitalization, and death, respectively. Effectiveness of a third dose of mRNA-1273 compared with the primary series was 37.1% (95% CI, 32.2-41.7), 63.5% (95% CI, 53.7-71.6), and 75.0% (95% CI, 55.4-88.0) against infection, hospitalization, and death, respectively. CONCLUSIONS: BNT162b2 and mRNA-1273 were effective against COVID-19 following emergence of Omicron variant. A third dose provided additional protection over the primary series. SN - 1537-6591 UR - https://www.unboundmedicine.com/medline/citation/35475889/Effectiveness_of_Messenger_RNA_based_Vaccines_During_the_Emergence_of_the_Severe_Acute_Respiratory_Syndrome_Coronavirus_2_Omicron_Variant_ DB - PRIME DP - Unbound Medicine ER -