Post-vaccination infection rates and modification of COVID-19 symptoms in vaccinated UK school-aged children and adolescents: A prospective longitudinal cohort study.

BNT162b2 vaccine effectiveness BNT162b2, Comirnaty SARS-CoV-2 vaccine (BioNTech, Pfizer) CA, Children and adolescents COVID-19 vaccination KCL, King's College London LFAT, Lateral flow antigen test OR, Odds Ratio PCR, Polymerase chain reaction Paediatrics SARS-CoV-2 vaccination SARS-CoV-2 vaccination in children SARS-CoV-2, Severe acute respiratory syndrome‐related coronavirus 2 UK, United Kingdom of Great Britain and Northern Ireland

Journal

The Lancet regional health. Europe
ISSN: 2666-7762
Titre abrégé: Lancet Reg Health Eur
Pays: England
ID NLM: 101777707

Informations de publication

Date de publication:
Aug 2022
Historique:
entrez: 13 7 2022
pubmed: 14 7 2022
medline: 14 7 2022
Statut: ppublish

Résumé

We aimed to explore the effectiveness of one-dose BNT162b2 vaccination upon SARS-CoV-2 infection, its effect on COVID-19 presentation, and post-vaccination symptoms in children and adolescents (CA) in the UK during periods of Delta and Omicron variant predominance. In this prospective longitudinal cohort study, we analysed data from 115,775 CA aged 12-17 years, proxy-reported through the Covid Symptom Study (CSS) smartphone application. We calculated post-vaccination infection risk after one dose of BNT162b2, and described the illness profile of CA with post-vaccination SARS-CoV-2 infection, compared to unvaccinated CA, and post-vaccination side-effects. Between August 5, 2021 and February 14, 2022, 25,971 UK CA aged 12-17 years received one dose of BNT162b2 vaccine. The probability of testing positive for infection diverged soon after vaccination, and was lower in CA with prior SARS-CoV-2 infection. Vaccination reduced proxy-reported infection risk (-80·4% (95% CI -0·82 -0·78) and -53·7% (95% CI -0·62 -0·43) at 14-30 days with Delta and Omicron variants respectively, and -61·5% (95% CI -0·74 -0·44) and -63·7% (95% CI -0·68 -0.59) after 61-90 days). Vaccinated CA who contracted SARS-CoV-2 during the Delta period had milder disease than unvaccinated CA; during the Omicron period this was only evident in children aged 12-15 years. Overall disease profile was similar in both vaccinated and unvaccinated CA. Post-vaccination local side-effects were common, systemic side-effects were uncommon, and both resolved within few days (3 days in most cases). One dose of BNT162b2 vaccine reduced risk of SARS-CoV-2 infection for at least 90 days in CA aged 12-17 years. Vaccine protection varied for SARS-CoV-2 variant type (lower for Omicron than Delta variant), and was enhanced by pre-vaccination SARS-CoV-2 infection. Severity of COVID-19 presentation after vaccination was generally milder, although unvaccinated CA also had generally mild disease. Overall, vaccination was well-tolerated. UK Government Department of Health and Social Care, Chronic Disease Research Foundation, The Wellcome Trust, UK Engineering and Physical Sciences Research Council, UK Research and Innovation London Medical Imaging & Artificial Intelligence Centre for Value Based Healthcare, UK National Institute for Health Research, UK Medical Research Council, British Heart Foundation and Alzheimer's Society, and ZOE Limited.

Sections du résumé

Background UNASSIGNED
We aimed to explore the effectiveness of one-dose BNT162b2 vaccination upon SARS-CoV-2 infection, its effect on COVID-19 presentation, and post-vaccination symptoms in children and adolescents (CA) in the UK during periods of Delta and Omicron variant predominance.
Methods UNASSIGNED
In this prospective longitudinal cohort study, we analysed data from 115,775 CA aged 12-17 years, proxy-reported through the Covid Symptom Study (CSS) smartphone application. We calculated post-vaccination infection risk after one dose of BNT162b2, and described the illness profile of CA with post-vaccination SARS-CoV-2 infection, compared to unvaccinated CA, and post-vaccination side-effects.
Findings UNASSIGNED
Between August 5, 2021 and February 14, 2022, 25,971 UK CA aged 12-17 years received one dose of BNT162b2 vaccine. The probability of testing positive for infection diverged soon after vaccination, and was lower in CA with prior SARS-CoV-2 infection. Vaccination reduced proxy-reported infection risk (-80·4% (95% CI -0·82 -0·78) and -53·7% (95% CI -0·62 -0·43) at 14-30 days with Delta and Omicron variants respectively, and -61·5% (95% CI -0·74 -0·44) and -63·7% (95% CI -0·68 -0.59) after 61-90 days). Vaccinated CA who contracted SARS-CoV-2 during the Delta period had milder disease than unvaccinated CA; during the Omicron period this was only evident in children aged 12-15 years. Overall disease profile was similar in both vaccinated and unvaccinated CA. Post-vaccination local side-effects were common, systemic side-effects were uncommon, and both resolved within few days (3 days in most cases).
Interpretation UNASSIGNED
One dose of BNT162b2 vaccine reduced risk of SARS-CoV-2 infection for at least 90 days in CA aged 12-17 years. Vaccine protection varied for SARS-CoV-2 variant type (lower for Omicron than Delta variant), and was enhanced by pre-vaccination SARS-CoV-2 infection. Severity of COVID-19 presentation after vaccination was generally milder, although unvaccinated CA also had generally mild disease. Overall, vaccination was well-tolerated.
Funding UNASSIGNED
UK Government Department of Health and Social Care, Chronic Disease Research Foundation, The Wellcome Trust, UK Engineering and Physical Sciences Research Council, UK Research and Innovation London Medical Imaging & Artificial Intelligence Centre for Value Based Healthcare, UK National Institute for Health Research, UK Medical Research Council, British Heart Foundation and Alzheimer's Society, and ZOE Limited.

Identifiants

pubmed: 35821715
doi: 10.1016/j.lanepe.2022.100429
pii: S2666-7762(22)00123-5
pmc: PMC9263281
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100429

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom

Informations de copyright

© 2022 The Author(s).

Déclaration de conflit d'intérêts

JCP, LP, AM, JW are employees of Zoe Limited. TDS and SO report being consultants for Zoe Limited, during the conduct of the study. All other authors have nothing to declare.

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Auteurs

Erika Molteni (E)

School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.

Liane S Canas (LS)

School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.

Kerstin Kläser (K)

School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.

Jie Deng (J)

School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.

Sunil S Bhopal (SS)

Population Health Sciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, Tyne and Wear, UK.

Robert C Hughes (RC)

Department of Population Health, Faculty of Epidemiology & Population Health, London School of Hygiene & Tropical Medicine, Keppel Street, London, UK.

Liyuan Chen (L)

School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.

Benjamin Murray (B)

School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.

Eric Kerfoot (E)

School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.

Michela Antonelli (M)

School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.

Carole H Sudre (CH)

School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
MRC Unit for Lifelong Health and Ageing, Department of Population Health Sciences and Centre for Medical Image Computing, Department of Computer Science, University College London, London, UK.

Joan Capdevila Pujol (JC)

Zoe Limited, London, UK.

Lorenzo Polidori (L)

Zoe Limited, London, UK.

Anna May (A)

Zoe Limited, London, UK.

Prof Alexander Hammers (PA)

School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.

Jonathan Wolf (J)

Zoe Limited, London, UK.

Prof Tim D Spector (PTD)

Department of Twin Research and Genetic Epidemiology, King's College London, London, UK.

Claire J Steves (CJ)

Department of Twin Research and Genetic Epidemiology, King's College London, London, UK.
Department of Aging and Health, Guy's and St Thomas' NHS Foundation Trust, London, UK.

Prof Sebastien Ourselin (PS)

School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.

Michael Absoud (M)

Children's Neurosciences, Evelina London Children's Hospital, St Thomas' Hospital, King's Health Partners, Academic Health Science Centre, London, UK.
Department of Women and Children's Health, Faculty of Life Sciences and Medicine, School of Life Course Sciences, King's College London, London, UK.

Marc Modat (M)

School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.

Prof Emma L Duncan (PEL)

Department of Twin Research and Genetic Epidemiology, King's College London, London, UK.
Department of Endocrinology, Guy's and St Thomas' NHS Foundation trust, London, UK.

Classifications MeSH