Community seroprevalence of SARS-CoV-2 in children and adolescents in England, 2019-2021.

COVID-19 epidemiology healthcare disparities paediatrics

Journal

Archives of disease in childhood
ISSN: 1468-2044
Titre abrégé: Arch Dis Child
Pays: England
ID NLM: 0372434

Informations de publication

Date de publication:
20 Jul 2022
Historique:
received: 05 05 2022
accepted: 23 06 2022
entrez: 20 7 2022
pubmed: 21 7 2022
medline: 21 7 2022
Statut: aheadofprint

Résumé

To understand community seroprevalence of SARS-CoV-2 in children and adolescents. This is vital to understanding the susceptibility of this cohort to COVID-19 and to inform public health policy for disease control such as immunisation. We conducted a community-based cross-sectional seroprevalence study in participants aged 0-18 years old recruiting from seven regions in England between October 2019 and June 2021 and collecting extensive demographic and symptom data. Serum samples were tested for antibodies against SARS-CoV-2 spike and nucleocapsid proteins using Roche assays processed at UK Health Security Agency laboratories. Prevalence estimates were calculated for six time periods and were standardised by age group, ethnicity and National Health Service region. Post-first wave (June-August 2020), the (anti-spike IgG) adjusted seroprevalence was 5.2%, varying from 0.9% (participants 10-14 years old) to 9.5% (participants 5-9 years old). By April-June 2021, this had increased to 19.9%, varying from 13.9% (participants 0-4 years old) to 32.7% (participants 15-18 years old). Minority ethnic groups had higher risk of SARS-CoV-2 seropositivity than white participants (OR 1.4, 95% CI 1.0 to 2.0), after adjusting for sex, age, region, time period, deprivation and urban/rural geography. In children <10 years, there were no symptoms or symptom clusters that reliably predicted seropositivity. Overall, 48% of seropositive participants with complete questionnaire data recalled no symptoms between February 2020 and their study visit. Approximately one-third of participants aged 15-18 years old had evidence of antibodies against SARS-CoV-2 prior to the introduction of widespread vaccination. These data demonstrate that ethnic background is independently associated with risk of SARS-CoV-2 infection in children. NCT04061382.

Identifiants

pubmed: 35858775
pii: archdischild-2022-324375
doi: 10.1136/archdischild-2022-324375
pmc: PMC9887370
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT04061382']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Medical Research Council
ID : MC_PC_19081
Pays : United Kingdom

Informations de copyright

© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: MDS acts on behalf of the University of Oxford as an investigator on studies funded or sponsored by vaccine manufacturers, including AstraZeneca, GlaxoSmithKline, Pfizer, Novavax, Janssen, Medimmune and MCM. He receives no personal financial payment for this work. SNF acts on behalf of University Hospital Southampton National Health Service (NHS) Foundation Trust as an investigator or providing consultative advice, or both, on clinical trials and studies of COVID-19 and other vaccines funded or sponsored by vaccine manufacturers including Janssen, Pfizer, AstraZeneca, GlaxoSmithKline, Novavax, Seqirus, Sanofi, Medimmune, Merck and Valneva. He receives no personal financial payment for this work. MR and EL, through the Immunisation Department, provide vaccine manufacturers (including Pfizer) with post-marketing surveillance reports about pneumococcal and meningococcal disease which the companies are required to submit to the UK Licensing authority in compliance with their Risk Management Strategy. A cost recovery charge is made for these reports. PA acts on behalf of the University of Oxford as the director of operations at the Oxford Vaccine Group and has received funding from the Vaccine Taskforce via the NIHR and AstraZeneca.

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Auteurs

Helen Ratcliffe (H)

Department of Paediatrics, University of Oxford, Oxford, UK helen.ratcliffe@paediatrics.ox.ac.uk.

K S Tiley (KS)

Department of Paediatrics, University of Oxford, Oxford, UK.

Nick Andrews (N)

Statistics, Modelling and Economics Department, Health Protection Agency, London, UK.

Gayatri Amirthalingam (G)

Immunisation, Hepatitis and Blood Safety Department, Public Health England, London, UK.

I Vichos (I)

Department of Paediatrics, University of Oxford, Oxford, UK.

E Morey (E)

Department of Paediatrics, University of Oxford, Oxford, UK.

N L Douglas (NL)

Department of Paediatrics, University of Oxford, Oxford, UK.

S Marinou (S)

Department of Paediatrics, University of Oxford, Oxford, UK.

Emma Plested (E)

Department of Paediatrics, University of Oxford, Oxford, UK.

Parvinder Aley (P)

Department of Paediatrics, University of Oxford, Oxford, UK.

Eva P Galiza (EP)

St George's Vaccine Institute, St. George's University Hospitals NHS Foundation Trust, London, UK.

Saul N Faust (SN)

Academic Unit of Clinical & Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.
NIHR Wellcome Trust Clinical Research Facility, University Hospital Southampton NHS Foundation Trust, Southampton, UK.

S Hughes (S)

Department of Paediatrics, Royal Manchester Children's Hospital, Manchester, UK.

Clare S Murray (CS)

Department of Paediatrics, Royal Manchester Children's Hospital, Manchester, UK.
Respiratory Group, University of Manchester, Manchester, UK.

Marion Roderick (M)

Paediatric Infectious Diseases and Immunology, University Hospitals Bristol NHS Foundation Trust, Bristol, UK.

Fiona Shackley (F)

Immunology, Allergy and Infectious Diseases, Sheffield Children's Hospital NHS Foundation Trust, Sheffield, UK.

Sam J Oddie (SJ)

Bradford Neonatology, Bradford Teaching Hospitals NHS Foundation Trust, West Yorkshire, UK.

Tim Lees (T)

Paediatric Respiratory Medicine, Leeds Teaching Hospitals NHS Trust, Leeds, UK.

D P J Turner (DPJ)

School of Life Sciences, University of Nottingham and Nottingham University Hospitals NHS Trust, Nottingham, UK.

M Raman (M)

Department of Paediatrics, University Hospitals Plymouth NHS Trust, Plymouth, UK.

Stephen Owens (S)

Paediatric Immunology and Infectious Diseases, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK.

Paul Turner (P)

Section of Paediatrics, Imperial College London, London, UK.

H Cockerill (H)

Department of Paediatrics, West Suffolk NHS Foundation Trust, Bury Saint Edmunds, UK.

J Lopez Bernal (J)

Immunisation, Hepatitis and Blood Safety Department, Public Health England, London, UK.

E Linley (E)

Vaccine Evaluation Unit, UK Health Security Agency, London, UK.

Ray Borrow (R)

Vaccine Evaluation Unit, UK Health Security Agency, London, UK.

Kevin Brown (K)

Virus Reference Department, Public Health England, Colindale, UK.

Mary Elizabeth Ramsay (ME)

Immunisation, Hepatitis and Blood Safety Department, Public Health England, London, UK.

M Voysey (M)

Department of Paediatrics, University of Oxford, Oxford, UK.

Matthew D Snape (MD)

Department of Paediatrics, University of Oxford, Oxford, UK.

Classifications MeSH