Quantitative SARS-CoV-2 anti-spike responses to Pfizer-BioNTech and Oxford-AstraZeneca vaccines by previous infection status.


Journal

Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases
ISSN: 1469-0691
Titre abrégé: Clin Microbiol Infect
Pays: England
ID NLM: 9516420

Informations de publication

Date de publication:
Oct 2021
Historique:
received: 21 03 2021
revised: 23 05 2021
accepted: 25 05 2021
pubmed: 11 6 2021
medline: 16 10 2021
entrez: 10 6 2021
Statut: ppublish

Résumé

We investigated determinants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) anti-spike IgG responses in healthcare workers (HCWs) following one or two doses of Pfizer-BioNTech or Oxford-AstraZeneca vaccines. HCWs participating in regular SARS-CoV-2 PCR and antibody testing were invited for serological testing prior to first and second vaccination, and 4 weeks post-vaccination if receiving a 12-week dosing interval. Quantitative post-vaccination anti-spike antibody responses were measured using the Abbott SARS-CoV-2 IgG II Quant assay (detection threshold: ≥50 AU/mL). We used multivariable logistic regression to identify predictors of seropositivity and generalized additive models to track antibody responses over time. 3570/3610 HCWs (98.9%) were seropositive >14 days post first vaccination and prior to second vaccination: 2706/2720 (99.5%) were seropositive after the Pfizer-BioNTech and 864/890 (97.1%) following the Oxford-AstraZeneca vaccines. Previously infected and younger HCWs were more likely to test seropositive post first vaccination, with no evidence of differences by sex or ethnicity. All 470 HCWs tested >14 days after the second vaccination were seropositive. Quantitative antibody responses were higher after previous infection: median (IQR) >21 days post first Pfizer-BioNTech 14 604 (7644-22 291) AU/mL versus 1028 (564-1985) AU/mL without prior infection (p < 0.001). Oxford-AstraZeneca vaccine recipients had lower readings post first dose than Pfizer-BioNTech recipients, with and without previous infection, 10 095 (5354-17 096) and 435 (203-962) AU/mL respectively (both p < 0.001 versus Pfizer-BioNTech). Antibody responses >21 days post second Pfizer vaccination in those not previously infected, 10 058 (6408-15 582) AU/mL, were similar to those after prior infection followed by one vaccine dose. SARS-CoV-2 vaccination leads to detectable anti-spike antibodies in nearly all adult HCWs. Whether differences in response impact vaccine efficacy needs further study.

Identifiants

pubmed: 34111577
pii: S1198-743X(21)00289-5
doi: 10.1016/j.cmi.2021.05.041
pmc: PMC8180449
pii:
doi:

Substances chimiques

Antibodies, Viral 0
COVID-19 Vaccines 0
Immunoglobulin G 0
Spike Glycoprotein, Coronavirus 0
spike protein, SARS-CoV-2 0
ChAdOx1 nCoV-19 B5S3K2V0G8
BNT162 Vaccine N38TVC63NU

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1516.e7-1516.e14

Subventions

Organisme : Medical Research Council
ID : MR/N00065X/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/V001329/1
Pays : United Kingdom

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier Ltd.. All rights reserved.

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Auteurs

David W Eyre (DW)

Oxford University Hospitals NHS Foundation Trust, Oxford, UK; Nuffield Department of Population Health, University of Oxford, Oxford, UK; NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, UK; NIHR Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance at University of Oxford in Partnership with Public Health England, Oxford, UK. Electronic address: david.eyre@bdi.ox.ac.uk.

Sheila F Lumley (SF)

Oxford University Hospitals NHS Foundation Trust, Oxford, UK; NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, UK; NIHR Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance at University of Oxford in Partnership with Public Health England, Oxford, UK; Nuffield Department of Medicine, University of Oxford, Oxford, UK.

Jia Wei (J)

Nuffield Department of Medicine, University of Oxford, Oxford, UK.

Stuart Cox (S)

Oxford University Hospitals NHS Foundation Trust, Oxford, UK.

Tim James (T)

Oxford University Hospitals NHS Foundation Trust, Oxford, UK.

Anita Justice (A)

Oxford University Hospitals NHS Foundation Trust, Oxford, UK.

Gerald Jesuthasan (G)

Oxford University Hospitals NHS Foundation Trust, Oxford, UK.

Denise O'Donnell (D)

Nuffield Department of Medicine, University of Oxford, Oxford, UK.

Alison Howarth (A)

Nuffield Department of Medicine, University of Oxford, Oxford, UK.

Stephanie B Hatch (SB)

Nuffield Department of Medicine, University of Oxford, Oxford, UK.

Brian D Marsden (BD)

Nuffield Department of Medicine, University of Oxford, Oxford, UK; Kennedy Institute of Rheumatology Research, University of Oxford, UK.

E Yvonne Jones (EY)

Nuffield Department of Medicine, University of Oxford, Oxford, UK.

David I Stuart (DI)

Nuffield Department of Medicine, University of Oxford, Oxford, UK.

Daniel Ebner (D)

Nuffield Department of Medicine, University of Oxford, Oxford, UK; Target Discovery Institute, University of Oxford, Oxford, UK.

Sarah Hoosdally (S)

NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, UK; NIHR Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance at University of Oxford in Partnership with Public Health England, Oxford, UK; Nuffield Department of Medicine, University of Oxford, Oxford, UK.

Derrick W Crook (DW)

Oxford University Hospitals NHS Foundation Trust, Oxford, UK; NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, UK; NIHR Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance at University of Oxford in Partnership with Public Health England, Oxford, UK; Nuffield Department of Medicine, University of Oxford, Oxford, UK.

Tim E A Peto (TEA)

Oxford University Hospitals NHS Foundation Trust, Oxford, UK; NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, UK; NIHR Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance at University of Oxford in Partnership with Public Health England, Oxford, UK; Nuffield Department of Medicine, University of Oxford, Oxford, UK.

Timothy M Walker (TM)

Nuffield Department of Medicine, University of Oxford, Oxford, UK; Oxford University Clinical Research Unit, Ho Chi Minh City, Viet nam.

Nicole E Stoesser (NE)

Oxford University Hospitals NHS Foundation Trust, Oxford, UK; NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, UK; NIHR Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance at University of Oxford in Partnership with Public Health England, Oxford, UK; Nuffield Department of Medicine, University of Oxford, Oxford, UK.

Philippa C Matthews (PC)

Oxford University Hospitals NHS Foundation Trust, Oxford, UK; NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, UK; NIHR Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance at University of Oxford in Partnership with Public Health England, Oxford, UK; Nuffield Department of Medicine, University of Oxford, Oxford, UK.

Koen B Pouwels (KB)

Nuffield Department of Population Health, University of Oxford, Oxford, UK; NIHR Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance at University of Oxford in Partnership with Public Health England, Oxford, UK.

A Sarah Walker (AS)

NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, UK; NIHR Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance at University of Oxford in Partnership with Public Health England, Oxford, UK; Nuffield Department of Medicine, University of Oxford, Oxford, UK.

Katie Jeffery (K)

Oxford University Hospitals NHS Foundation Trust, Oxford, UK.

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Classifications MeSH