Estimating long-term vaccine effectiveness against SARS-CoV-2 variants: a model-based approach.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
19 07 2023
Historique:
received: 06 01 2023
accepted: 27 06 2023
medline: 21 7 2023
pubmed: 20 7 2023
entrez: 19 7 2023
Statut: epublish

Résumé

With the ongoing evolution of the SARS-CoV-2 virus updated vaccines may be needed. We fitted a model linking immunity levels and protection to vaccine effectiveness data from England for three vaccines (Oxford/AstraZeneca AZD1222, Pfizer-BioNTech BNT162b2, Moderna mRNA-1273) and two variants (Delta, Omicron). Our model reproduces the observed sustained protection against hospitalisation and death from the Omicron variant over the first six months following dose 3 with the ancestral vaccines but projects a gradual waning to moderate protection after 1 year. Switching the fourth dose to a variant-matched vaccine against Omicron BA.1/2 is projected to prevent nearly twice as many hospitalisations and deaths over a 1-year period compared to administering the ancestral vaccine. This result is sensitive to the degree to which immunogenicity data can be used to predict vaccine effectiveness and uncertainty regarding the impact that infection-induced immunity (not captured here) may play in modifying future vaccine effectiveness.

Identifiants

pubmed: 37468463
doi: 10.1038/s41467-023-39736-3
pii: 10.1038/s41467-023-39736-3
pmc: PMC10356855
doi:

Substances chimiques

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

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

4325

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Department of Health
ID : NIHR200908
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/R015600/1
Pays : United Kingdom

Informations de copyright

© 2023. The Author(s).

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Auteurs

Alexandra B Hogan (AB)

School of Population Health, Faculty of Medicine and Health, University of New South Wales, Sydney, NSW, Australia.
MRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.

Patrick Doohan (P)

MRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.

Sean L Wu (SL)

Institute for Health Metrics and Evaluation, University of Washington, Seattle, USA.

Daniela Olivera Mesa (DO)

MRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.

Jaspreet Toor (J)

MRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.

Oliver J Watson (OJ)

MRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.
London School of Hygiene and Tropical Medicine, London, UK.

Peter Winskill (P)

MRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.

Giovanni Charles (G)

MRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.

Gregory Barnsley (G)

MRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.
London School of Hygiene and Tropical Medicine, London, UK.

Eleanor M Riley (EM)

Institute of Immunology and Infection Research, School of Biological Sciences, University of Edinburgh, Edinburgh, UK.

David S Khoury (DS)

Kirby Institute, University of New South Wales, Sydney, NSW, Australia.

Neil M Ferguson (NM)

MRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.

Azra C Ghani (AC)

MRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK. a.ghani@imperial.ac.uk.

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