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Post-vaccination infection rates and modification of COVID-19 symptoms in vaccinated UK school-aged children and adolescents: A prospective longitudinal cohort study.
Molteni, Erika; Canas, Liane S; Kläser, Kerstin; Deng, Jie; Bhopal, Sunil S; Hughes, Robert C; Chen, Liyuan; Murray, Benjamin; Kerfoot, Eric; Antonelli, Michela; Sudre, Carole H; Pujol, Joan Capdevila; Polidori, Lorenzo; May, Anna; Hammers, Prof Alexander; Wolf, Jonathan; Spector, Prof Tim D; Steves, Claire J; Ourselin, Prof Sebastien; Absoud, Michael; Modat, Marc; Duncan, Prof Emma L.
  • Molteni E; School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
  • Canas LS; School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
  • Kläser K; School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
  • Deng J; School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
  • Bhopal SS; Population Health Sciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, Tyne and Wear, UK.
  • Hughes RC; Department of Population Health, Faculty of Epidemiology & Population Health, London School of Hygiene & Tropical Medicine, Keppel Street, London, UK.
  • Chen L; School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
  • Murray B; School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
  • Kerfoot E; School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
  • Antonelli M; School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
  • Sudre CH; School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
  • Pujol JC; 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.
  • Polidori L; Zoe Limited, London, UK.
  • May A; Zoe Limited, London, UK.
  • Hammers PA; Zoe Limited, London, UK.
  • Wolf J; School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
  • Spector PTD; Zoe Limited, London, UK.
  • Steves CJ; Department of Twin Research and Genetic Epidemiology, King's College London, London, UK.
  • Ourselin PS; Department of Twin Research and Genetic Epidemiology, King's College London, London, UK.
  • Absoud M; Department of Aging and Health, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Modat M; School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
  • Duncan PEL; Children's Neurosciences, Evelina London Children's Hospital, St Thomas' Hospital, King's Health Partners, Academic Health Science Centre, London, UK.
Lancet Reg Health Eur ; 19: 100429, 2022 Aug.
Article in English | MEDLINE | ID: covidwho-2004324
ABSTRACT

Background:

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:

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:

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:

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:

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.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines / Variants Language: English Journal: Lancet Reg Health Eur Year: 2022 Document Type: Article Affiliation country: J.lanepe.2022.100429

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines / Variants Language: English Journal: Lancet Reg Health Eur Year: 2022 Document Type: Article Affiliation country: J.lanepe.2022.100429