Effect of Delta variant on viral burden and vaccine effectiveness against new SARS-CoV-2 infections in the UK.


Journal

Nature medicine
ISSN: 1546-170X
Titre abrégé: Nat Med
Pays: United States
ID NLM: 9502015

Informations de publication

Date de publication:
12 2021
Historique:
received: 18 08 2021
accepted: 21 09 2021
pubmed: 16 10 2021
medline: 6 1 2022
entrez: 15 10 2021
Statut: ppublish

Résumé

The effectiveness of the BNT162b2 and ChAdOx1 vaccines against new severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections requires continuous re-evaluation, given the increasingly dominant B.1.617.2 (Delta) variant. In this study, we investigated the effectiveness of these vaccines in a large, community-based survey of randomly selected households across the United Kingdom. We found that the effectiveness of BNT162b2 and ChAdOx1 against infections (new polymerase chain reaction (PCR)-positive cases) with symptoms or high viral burden is reduced with the B.1.617.2 variant (absolute difference of 10-13% for BNT162b2 and 16% for ChAdOx1) compared to the B.1.1.7 (Alpha) variant. The effectiveness of two doses remains at least as great as protection afforded by prior natural infection. The dynamics of immunity after second doses differed significantly between BNT162b2 and ChAdOx1, with greater initial effectiveness against new PCR-positive cases but faster declines in protection against high viral burden and symptomatic infection with BNT162b2. There was no evidence that effectiveness varied by dosing interval, but protection was higher in vaccinated individuals after a prior infection and in younger adults. With B.1.617.2, infections occurring after two vaccinations had similar peak viral burden as those in unvaccinated individuals. SARS-CoV-2 vaccination still reduces new infections, but effectiveness and attenuation of peak viral burden are reduced with B.1.617.2.

Identifiants

pubmed: 34650248
doi: 10.1038/s41591-021-01548-7
pii: 10.1038/s41591-021-01548-7
pmc: PMC8674129
doi:

Substances chimiques

Antibodies, Neutralizing 0
Antibodies, Viral 0
ChAdOx1 nCoV-19 B5S3K2V0G8
BNT162 Vaccine N38TVC63NU

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

2127-2135

Subventions

Organisme : RCUK | Medical Research Council (MRC)
ID : MC_UU_12023/22
Organisme : Wellcome Trust (Wellcome)
ID : 110110/Z/15/Z
Organisme : Medical Research Council
ID : MR/V038613/1
Pays : United Kingdom
Organisme : DH | National Institute for Health Research (NIHR)
ID : NIHR200915
Organisme : Wellcome Trust
Pays : United Kingdom

Informations de copyright

© 2021. The Author(s).

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Auteurs

Koen B Pouwels (KB)

National Institute for Health Research Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance, University of Oxford, Oxford, UK. koen.pouwels@ndph.ox.ac.uk.
Health Economics Research Centre, Nuffield Department of Population Health, University of Oxford, Oxford, UK. koen.pouwels@ndph.ox.ac.uk.

Emma Pritchard (E)

National Institute for Health Research Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance, University of Oxford, Oxford, UK.
Nuffield Department of Medicine, University of Oxford, Oxford, UK.

Philippa C Matthews (PC)

Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Department of Infectious Diseases and Microbiology, Oxford University Hospitals NHS Foundation Trust, John Radcliffe Hospital, Oxford, UK.
National Institute for Health Research Oxford Biomedical Research Centre, University of Oxford, Oxford, UK.

Nicole Stoesser (N)

National Institute for Health Research Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance, University of Oxford, Oxford, UK.
Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Department of Infectious Diseases and Microbiology, Oxford University Hospitals NHS Foundation Trust, John Radcliffe Hospital, Oxford, UK.
National Institute for Health Research Oxford Biomedical Research Centre, University of Oxford, Oxford, UK.

David W Eyre (DW)

National Institute for Health Research Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance, University of Oxford, Oxford, UK.
Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Department of Infectious Diseases and Microbiology, Oxford University Hospitals NHS Foundation Trust, John Radcliffe Hospital, Oxford, UK.
Big Data Institute, Nuffield Department of Population Health, University of Oxford, Oxford, UK.

Karina-Doris Vihta (KD)

National Institute for Health Research Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance, University of Oxford, Oxford, UK.
Department of Engineering, University of Oxford, Oxford, UK.

Thomas House (T)

Department of Mathematics, University of Manchester, Manchester, UK.
IBM Research, Hartree Centre, Sci-Tech Daresbury, UK.

Jodie Hay (J)

Glasgow Lighthouse Laboratory, Glasgow, UK.
University of Glasgow, Glasgow, UK.

John I Bell (JI)

Office of the Regius Professor of Medicine, University of Oxford, Oxford, UK.

John N Newton (JN)

Health Improvement Directorate, Public Health England, London, UK.

Jeremy Farrar (J)

Wellcome Trust, London, UK.

Derrick Crook (D)

National Institute for Health Research Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance, University of Oxford, Oxford, UK.
Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Department of Infectious Diseases and Microbiology, Oxford University Hospitals NHS Foundation Trust, John Radcliffe Hospital, Oxford, UK.
National Institute for Health Research Oxford Biomedical Research Centre, University of Oxford, Oxford, UK.

Duncan Cook (D)

Office for National Statistics, Newport, UK.

Emma Rourke (E)

Office for National Statistics, Newport, UK.

Ruth Studley (R)

Office for National Statistics, Newport, UK.

Tim E A Peto (TEA)

National Institute for Health Research Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance, University of Oxford, Oxford, UK.
Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Department of Infectious Diseases and Microbiology, Oxford University Hospitals NHS Foundation Trust, John Radcliffe Hospital, Oxford, UK.
National Institute for Health Research Oxford Biomedical Research Centre, University of Oxford, Oxford, UK.

Ian Diamond (I)

Office for National Statistics, Newport, UK.

A Sarah Walker (AS)

National Institute for Health Research Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance, University of Oxford, Oxford, UK.
Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Department of Infectious Diseases and Microbiology, Oxford University Hospitals NHS Foundation Trust, John Radcliffe Hospital, Oxford, UK.
MRC Clinical Trials Unit at UCL, University College London, London, UK.

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