SARS-CoV-2 infection and vaccine effectiveness in England (REACT-1): a series of cross-sectional random community surveys.


Journal

The Lancet. Respiratory medicine
ISSN: 2213-2619
Titre abrégé: Lancet Respir Med
Pays: England
ID NLM: 101605555

Informations de publication

Date de publication:
04 2022
Historique:
received: 26 10 2021
revised: 18 11 2021
accepted: 22 11 2021
pubmed: 28 1 2022
medline: 6 4 2022
entrez: 27 1 2022
Statut: ppublish

Résumé

England has experienced a third wave of the COVID-19 epidemic since the end of May, 2021, coinciding with the rapid spread of the delta (B.1.617.2) variant, despite high levels of vaccination among adults. Vaccination rates (single dose) in England are lower among children aged 16-17 years and 12-15 years, whose vaccination in England commenced in August and September, 2021, respectively. We aimed to analyse the underlying dynamics driving patterns in SARS-CoV-2 prevalence during September, 2021, in England. The REal-time Assessment of Community Transmission-1 (REACT-1) study, which commenced data collection in May, 2020, involves a series of random cross-sectional surveys in the general population of England aged 5 years and older. Using RT-PCR swab positivity data from 100 527 participants with valid throat and nose swabs in round 14 of REACT-1 (Sept 9-27, 2021), we estimated community-based prevalence of SARS-CoV-2 and vaccine effectiveness against infection by combining round 14 data with data from round 13 (June 24 to July 12, 2021; n=172 862). During September, 2021, we estimated a mean RT-PCR positivity rate of 0·83% (95% CrI 0·76-0·89), with a reproduction number (R) overall of 1·03 (95% CrI 0·94-1·14). Among the 475 (62·2%) of 764 sequenced positive swabs, all were of the delta variant; 22 (4·63%; 95% CI 3·07-6·91) included the Tyr145His mutation in the spike protein associated with the AY.4 sublineage, and there was one Glu484Lys mutation. Age, region, key worker status, and household size jointly contributed to the risk of swab positivity. The highest weighted prevalence was observed among children aged 5-12 years, at 2·32% (95% CrI 1·96-2·73) and those aged 13-17 years, at 2·55% (2·11-3·08). The SARS-CoV-2 epidemic grew in those aged 5-11 years, with an R of 1·42 (95% CrI 1·18-1·68), but declined in those aged 18-54 years, with an R of 0·81 (0·68-0·97). At ages 18-64 years, the adjusted vaccine effectiveness against infection was 62·8% (95% CI 49·3-72·7) after two doses compared to unvaccinated people, for all vaccines combined, 44·8% (22·5-60·7) for the ChAdOx1 nCov-19 (Oxford-AstraZeneca) vaccine, and 71·3% (56·6-81·0) for the BNT162b2 (Pfizer-BioNTech) vaccine. In individuals aged 18 years and older, the weighted prevalence of swab positivity was 0·35% (95% CrI 0·31-0·40) if the second dose was administered up to 3 months before their swab but 0·55% (0·50-0·61) for those who received their second dose 3-6 months before their swab, compared to 1·76% (1·60-1·95) among unvaccinated individuals. In September, 2021, at the start of the autumn school term in England, infections were increasing exponentially in children aged 5-17 years, at a time when vaccination rates were low in this age group. In adults, compared to those who received their second dose less than 3 months ago, the higher prevalence of swab positivity at 3-6 months following two doses of the COVID-19 vaccine suggests an increased risk of breakthrough infections during this period. The vaccination programme needs to reach children as well as unvaccinated and partially vaccinated adults to reduce SARS-CoV-2 transmission and associated disruptions to work and education. Department of Health and Social Care, England.

Sections du résumé

BACKGROUND
England has experienced a third wave of the COVID-19 epidemic since the end of May, 2021, coinciding with the rapid spread of the delta (B.1.617.2) variant, despite high levels of vaccination among adults. Vaccination rates (single dose) in England are lower among children aged 16-17 years and 12-15 years, whose vaccination in England commenced in August and September, 2021, respectively. We aimed to analyse the underlying dynamics driving patterns in SARS-CoV-2 prevalence during September, 2021, in England.
METHODS
The REal-time Assessment of Community Transmission-1 (REACT-1) study, which commenced data collection in May, 2020, involves a series of random cross-sectional surveys in the general population of England aged 5 years and older. Using RT-PCR swab positivity data from 100 527 participants with valid throat and nose swabs in round 14 of REACT-1 (Sept 9-27, 2021), we estimated community-based prevalence of SARS-CoV-2 and vaccine effectiveness against infection by combining round 14 data with data from round 13 (June 24 to July 12, 2021; n=172 862).
FINDINGS
During September, 2021, we estimated a mean RT-PCR positivity rate of 0·83% (95% CrI 0·76-0·89), with a reproduction number (R) overall of 1·03 (95% CrI 0·94-1·14). Among the 475 (62·2%) of 764 sequenced positive swabs, all were of the delta variant; 22 (4·63%; 95% CI 3·07-6·91) included the Tyr145His mutation in the spike protein associated with the AY.4 sublineage, and there was one Glu484Lys mutation. Age, region, key worker status, and household size jointly contributed to the risk of swab positivity. The highest weighted prevalence was observed among children aged 5-12 years, at 2·32% (95% CrI 1·96-2·73) and those aged 13-17 years, at 2·55% (2·11-3·08). The SARS-CoV-2 epidemic grew in those aged 5-11 years, with an R of 1·42 (95% CrI 1·18-1·68), but declined in those aged 18-54 years, with an R of 0·81 (0·68-0·97). At ages 18-64 years, the adjusted vaccine effectiveness against infection was 62·8% (95% CI 49·3-72·7) after two doses compared to unvaccinated people, for all vaccines combined, 44·8% (22·5-60·7) for the ChAdOx1 nCov-19 (Oxford-AstraZeneca) vaccine, and 71·3% (56·6-81·0) for the BNT162b2 (Pfizer-BioNTech) vaccine. In individuals aged 18 years and older, the weighted prevalence of swab positivity was 0·35% (95% CrI 0·31-0·40) if the second dose was administered up to 3 months before their swab but 0·55% (0·50-0·61) for those who received their second dose 3-6 months before their swab, compared to 1·76% (1·60-1·95) among unvaccinated individuals.
INTERPRETATION
In September, 2021, at the start of the autumn school term in England, infections were increasing exponentially in children aged 5-17 years, at a time when vaccination rates were low in this age group. In adults, compared to those who received their second dose less than 3 months ago, the higher prevalence of swab positivity at 3-6 months following two doses of the COVID-19 vaccine suggests an increased risk of breakthrough infections during this period. The vaccination programme needs to reach children as well as unvaccinated and partially vaccinated adults to reduce SARS-CoV-2 transmission and associated disruptions to work and education.
FUNDING
Department of Health and Social Care, England.

Identifiants

pubmed: 35085490
pii: S2213-2600(21)00542-7
doi: 10.1016/S2213-2600(21)00542-7
pmc: PMC8786320
pii:
doi:

Substances chimiques

COVID-19 Vaccines 0
ChAdOx1 nCoV-19 B5S3K2V0G8
BNT162 Vaccine N38TVC63NU

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

355-366

Subventions

Organisme : Medical Research Council
ID : MR/L01341X/1
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 200861/Z/16/Z
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_PC_19012
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/R012504/1
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 200187/Z/15/Z
Pays : United Kingdom
Organisme : NCEZID CDC HHS
ID : U01 CK000505
Pays : United States
Organisme : Wellcome Trust
ID : 205456/Z/16/Z
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/J008761/1
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BBS/E/F/000PR10352
Pays : United Kingdom
Organisme : British Heart Foundation
ID : RE/18/4/34215
Pays : United Kingdom
Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/R015600/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_PC_19027
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/S019669/1
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2022 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. Published by Elsevier Ltd.. All rights reserved.

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Auteurs

Marc Chadeau-Hyam (M)

School of Public Health, Imperial College London, London, UK; MRC Centre for Environment and Health, School of Public Health, Imperial College London, London, UK.

Haowei Wang (H)

School of Public Health, Imperial College London, London, UK; MRC Centre for Global infectious Disease Analysis and Jameel Institute, Imperial College London, London, UK.

Oliver Eales (O)

School of Public Health, Imperial College London, London, UK; MRC Centre for Global infectious Disease Analysis and Jameel Institute, Imperial College London, London, UK.

David Haw (D)

School of Public Health, Imperial College London, London, UK; MRC Centre for Global infectious Disease Analysis and Jameel Institute, Imperial College London, London, UK.

Barbara Bodinier (B)

School of Public Health, Imperial College London, London, UK; MRC Centre for Environment and Health, School of Public Health, Imperial College London, London, UK.

Matthew Whitaker (M)

School of Public Health, Imperial College London, London, UK; MRC Centre for Environment and Health, School of Public Health, Imperial College London, London, UK.

Caroline E Walters (CE)

School of Public Health, Imperial College London, London, UK; MRC Centre for Global infectious Disease Analysis and Jameel Institute, Imperial College London, London, UK.

Kylie E C Ainslie (KEC)

School of Public Health, Imperial College London, London, UK; MRC Centre for Global infectious Disease Analysis and Jameel Institute, Imperial College London, London, UK; Centre for Infectious Disease Control, National Institute for Public Health and the Environment, Bilthoven, Netherlands.

Christina Atchison (C)

School of Public Health, Imperial College London, London, UK.

Claudio Fronterre (C)

CHICAS, Lancaster Medical School, Lancaster University, UK and Health Data Research, Lancaster, UK.

Peter J Diggle (PJ)

CHICAS, Lancaster Medical School, Lancaster University, UK and Health Data Research, Lancaster, UK.

Andrew J Page (AJ)

Quadram Institute, Norwich, UK.

Alexander J Trotter (AJ)

Quadram Institute, Norwich, UK.

Deborah Ashby (D)

School of Public Health, Imperial College London, London, UK.

Wendy Barclay (W)

Department of Infectious Disease, Imperial College London, London, UK.

Graham Taylor (G)

Department of Infectious Disease, Imperial College London, London, UK.

Graham Cooke (G)

Department of Infectious Disease, Imperial College London, London, UK; Imperial College Healthcare NHS Trust, London, UK; National Institute for Health Research Imperial Biomedical Research Centre, London, UK.

Helen Ward (H)

School of Public Health, Imperial College London, London, UK; Imperial College Healthcare NHS Trust, London, UK; National Institute for Health Research Imperial Biomedical Research Centre, London, UK.

Ara Darzi (A)

Imperial College Healthcare NHS Trust, London, UK; National Institute for Health Research Imperial Biomedical Research Centre, London, UK; Institute of Global Health Innovation, Imperial College London, London, UK.

Steven Riley (S)

School of Public Health, Imperial College London, London, UK; MRC Centre for Global infectious Disease Analysis and Jameel Institute, Imperial College London, London, UK.

Christl A Donnelly (CA)

School of Public Health, Imperial College London, London, UK; MRC Centre for Global infectious Disease Analysis and Jameel Institute, Imperial College London, London, UK; Department of Statistics, University of Oxford, Oxford, UK. Electronic address: c.donnelly@imperial.ac.uk.

Paul Elliott (P)

School of Public Health, Imperial College London, London, UK; MRC Centre for Environment and Health, School of Public Health, Imperial College London, London, UK; Imperial College Healthcare NHS Trust, London, UK; National Institute for Health Research Imperial Biomedical Research Centre, London, UK; Health Data Research (HDR) UK, Imperial College London, London, UK; UK Dementia Research Institute, Imperial College London, London, UK. Electronic address: p.elliott@imperial.ac.uk.

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