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Vaccine effectiveness of two-dose BNT162b2 against symptomatic and severe COVID-19 among adolescents in Brazil and Scotland over time: a test-negative case-control study.
Florentino, Pilar T V; Millington, Tristan; Cerqueira-Silva, Thiago; Robertson, Chris; de Araújo Oliveira, Vinicius; Júnior, Juracy B S; Alves, Flávia J O; Penna, Gerson O; Vital Katikireddi, Srinivasa; Boaventura, Viviane S; Werneck, Guilherme L; Pearce, Neil; McCowan, Colin; Sullivan, Christopher; Agrawal, Utkarsh; Grange, Zoe; Ritchie, Lewis D; Simpson, Colin R; Sheikh, Aziz; Barreto, Mauricio L; Rudan, Igor; Barral-Netto, Manoel; Paixão, Enny S.
  • Florentino PTV; Centre of Data and Knowledge Integration for Health (CIDACS), Gonçalo Moniz Institute, Oswaldo Cruz Foundation, Salvador, Brazil; Biomedical Science Institute, University of São Paulo, São Paulo, Brazil. Electronic address: pilar.veras@fiocruz.br.
  • Millington T; Usher Institute, University of Edinburgh, Edinburgh, UK.
  • Cerqueira-Silva T; LIB and LEITV Laboratories, Instituto Gonçalo Moniz, Oswaldo Cruz Foundation, Salvador, Brazil; Faculty of Medicine, Federal University of Bahia, Salvador, Brazil.
  • Robertson C; Public Health Scotland, Glasgow, Scotland, UK.
  • de Araújo Oliveira V; Centre of Data and Knowledge Integration for Health (CIDACS), Gonçalo Moniz Institute, Oswaldo Cruz Foundation, Salvador, Brazil.
  • Júnior JBS; Institute of Collective Health, Federal University of Bahia, Salvador, Brazil.
  • Alves FJO; Centre of Data and Knowledge Integration for Health (CIDACS), Gonçalo Moniz Institute, Oswaldo Cruz Foundation, Salvador, Brazil.
  • Penna GO; Tropical Medicine Centre, University of Brasília, Fiocruz School of Government Brasília, Brasília, Brazil.
  • Vital Katikireddi S; MRC/CSO Social and Public Health Sciences Unit, University of Glasgow, Glasgow, UK.
  • Boaventura VS; LIB and LEITV Laboratories, Instituto Gonçalo Moniz, Oswaldo Cruz Foundation, Salvador, Brazil; Faculty of Medicine, Federal University of Bahia, Salvador, Brazil.
  • Werneck GL; Department of Epidemiology, Social Medicine Institute, State University of Rio de Janeiro, Rio de Janeiro, Brazil; Institute of Collective Health Studies, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
  • Pearce N; Faculty of Epidemiology and Population Health, London School of Hygiene & Tropical Medicine, London, UK.
  • McCowan C; School of Medicine, University of St Andrews, St Andrews, Scotland, UK.
  • Sullivan C; Public Health Scotland, Glasgow, Scotland, UK.
  • Agrawal U; School of Medicine, University of St Andrews, St Andrews, Scotland, UK.
  • Grange Z; Public Health Scotland, Glasgow, Scotland, UK.
  • Ritchie LD; Academic Primary Care, University of Aberdeen, Aberdeen, Scotland, UK.
  • Simpson CR; School of Health, Wellington Faculty of Health, Victoria University of Wellington, Wellington, New Zealand.
  • Sheikh A; Usher Institute, University of Edinburgh, Edinburgh, UK.
  • Barreto ML; Centre of Data and Knowledge Integration for Health (CIDACS), Gonçalo Moniz Institute, Oswaldo Cruz Foundation, Salvador, Brazil.
  • Rudan I; Usher Institute, University of Edinburgh, Edinburgh, UK.
  • Barral-Netto M; Centre of Data and Knowledge Integration for Health (CIDACS), Gonçalo Moniz Institute, Oswaldo Cruz Foundation, Salvador, Brazil; LIB and LEITV Laboratories, Instituto Gonçalo Moniz, Oswaldo Cruz Foundation, Salvador, Brazil.
  • Paixão ES; Faculty of Epidemiology and Population Health, London School of Hygiene & Tropical Medicine, London, UK.
Lancet Infect Dis ; 22(11): 1577-1586, 2022 11.
Article in English | MEDLINE | ID: covidwho-1977931
ABSTRACT

BACKGROUND:

Little is known about vaccine effectiveness over time among adolescents, especially against the SARS-CoV-2 omicron (B.1.1.529) variant. This study assessed the associations between time since two-dose vaccination with BNT162b2 and the occurrence of symptomatic SARS-CoV-2 infection and severe COVID-19 among adolescents in Brazil and Scotland.

METHODS:

We did test-negative, case-control studies in adolescents aged 12-17 years with COVID-19-related symptoms in Brazil and Scotland. We linked records of SARS-CoV-2 RT-PCR and antigen tests to national vaccination and clinical records. We excluded tests from individuals who did not have symptoms, were vaccinated before the start of the national vaccination programme, received vaccines other than BNT162b2 or a SARS-CoV-2 booster dose of any kind, or had an interval between their first and second dose of fewer than 21 days. Additionally, we excluded negative SARS-CoV-2 tests recorded within 14 days of a previous negative test, negative tests recorded within 7 days after a positive test, any test done within 90 days after a positive test, and tests with missing sex and location information. Cases (SARS-CoV-2 test-positive adolescents) and controls (test-negative adolescents) were drawn from a sample of individuals in whom tests were collected within 10 days of symptom onset. We estimated the adjusted odds ratio and vaccine effectiveness against symptomatic COVID-19 for both countries and against severe COVID-19 (hospitalisation or death) for Brazil across fortnightly periods.

FINDINGS:

We analysed 503 776 tests from 2 948 538 adolescents in Brazil between Sept 2, 2021, and April 19, 2022, and 127 168 tests from 404 673 adolescents in Scotland between Aug 6, 2021, and April 19, 2022. Vaccine effectiveness peaked at 14-27 days after the second dose in both countries during both waves, and was significantly lower against symptomatic infection during the omicron-dominant period in Brazil (64·7% [95% CI 63·0-66·3]) and in Scotland (82·6% [80·6-84·5]), than it was in the delta-dominant period (80·7% [95% CI 77·8-83·3] in Brazil and 92·8% [85·7-96·4] in Scotland). Vaccine efficacy started to decline from 27 days after the second dose for both countries, reducing to 5·9% (95% CI 2·2-9·4) in Brazil and 50·6% (42·7-57·4) in Scotland at 98 days or more during the omicron-dominant period. In Brazil, protection against severe disease remained above 80% from 28 days after the second dose and was 82·7% (95% CI 68·8-90·4) at 98 days or more after receiving the second dose.

INTERPRETATION:

We found waning vaccine protection of BNT162b2 against symptomatic COVID-19 infection among adolescents in Brazil and Scotland from 27 days after the second dose. However, protection against severe COVID-19 outcomes remained high at 98 days or more after the second dose in the omicron-dominant period. Booster doses for adolescents need to be considered.

FUNDING:

UK Research and Innovation (Medical Research Council), Scottish Government, Health Data Research UK BREATHE Hub, Fiocruz, Fazer o Bem Faz Bem programme, Brazilian National Research Council, and Wellcome Trust. TRANSLATION For the Portuguese translation of the abstract see Supplementary Materials section.
Subject(s)

Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Experimental Studies / Observational study / Prognostic study Topics: Vaccines / Variants Limits: Adolescent / Humans Country/Region as subject: South America / Brazil Language: English Journal: Lancet Infect Dis Journal subject: Communicable Diseases Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Experimental Studies / Observational study / Prognostic study Topics: Vaccines / Variants Limits: Adolescent / Humans Country/Region as subject: South America / Brazil Language: English Journal: Lancet Infect Dis Journal subject: Communicable Diseases Year: 2022 Document Type: Article