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Duration of protection of CoronaVac plus heterologous BNT162b2 booster in the Omicron period in Brazil.
Cerqueira-Silva, Thiago; de Araujo Oliveira, Vinicius; Paixão, Enny S; Júnior, Juracy Bertoldo; Penna, Gerson O; Werneck, Guilherme L; Pearce, Neil; Barreto, Maurício L; Boaventura, Viviane S; Barral-Netto, Manoel.
  • Cerqueira-Silva T; LIB and LEITV Laboratories, Instituto Gonçalo Moniz, Fiocruz, Salvador, Bahia, Brazil.
  • de Araujo Oliveira V; Universidade Federal da Bahia, Salvador, Bahia, Brazil.
  • Paixão ES; Universidade Federal da Bahia, Salvador, Bahia, Brazil.
  • Júnior JB; Center for Data and Knowledge Integration for Health (CIDACS), Instituto Gonçalo Moniz, Fiocruz, Salvador, Bahia, Brazil.
  • Penna GO; London School of Hygiene and Tropical Medicine, London, WC1E 7HT, UK.
  • Werneck GL; Universidade Federal da Bahia, Salvador, Bahia, Brazil.
  • Pearce N; Center for Data and Knowledge Integration for Health (CIDACS), Instituto Gonçalo Moniz, Fiocruz, Salvador, Bahia, Brazil.
  • Barreto ML; Núcleo de Medicina Tropical, Universidade de Brasília. Escola Fiocruz de Governo, Fiocruz, DF, Brazil.
  • Boaventura VS; Universidade do Estado do Rio de Janeiro, Rio de Janeiro, Brazil.
  • Barral-Netto M; Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Nat Commun ; 13(1): 4154, 2022 07 18.
Article in English | MEDLINE | ID: covidwho-1937434
ABSTRACT
To date, no information has been published on the effectiveness of inactivated whole-virus COVID-19 vaccines plus heterologous booster against symptomatic infection and severe outcomes (hospitalization or death) during the dominance of the SARS-CoV-2 Omicron variant period. We evaluated the vaccine effectiveness (VE) of CoronaVac plus BNT162b2 booster during the period of dominance of the Omicron variant in Brazil (January to April 2022). Using a test-negative design, we analysed data for 2,471,576 individuals tested during the Omicron variant's dominant period using a nationally linked database from Brazil. Compared to unvaccinated, vaccinees maintained protection against severe outcomes, with an estimated VE of 84.1% (95% CI83.2-84.9) at more than 120 days after BNT162b2 booster. Furthermore, while we detected a high level of protection against severe outcomes for individuals up to 79 years old, waning was observed for individuals aged ≥80 years, with VE decreasing from 81.3% (95% CI77.9-84.2) at 31-60 days to 72.9% (95% CI70.6-75.1) at 120 days or more after the booster dose. However, no significant protection against symptomatic infection was observed at this time period. In conclusion, except for individuals aged ≥80 years, CoronaVac plus a BNT162b2 booster dose offered high and durable protection against severe outcomes due to Omicron.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Vaccines / COVID-19 Type of study: Experimental Studies / Observational study Topics: Vaccines / Variants Limits: Humans Country/Region as subject: South America / Brazil Language: English Journal: Nat Commun Journal subject: Biology / Science Year: 2022 Document Type: Article Affiliation country: S41467-022-31839-7

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Vaccines / COVID-19 Type of study: Experimental Studies / Observational study Topics: Vaccines / Variants Limits: Humans Country/Region as subject: South America / Brazil Language: English Journal: Nat Commun Journal subject: Biology / Science Year: 2022 Document Type: Article Affiliation country: S41467-022-31839-7