Evaluation of QuantiFERON SARS-CoV-2 interferon-γ release assay following SARS-CoV-2 infection and vaccination.


Journal

Clinical and experimental immunology
ISSN: 1365-2249
Titre abrégé: Clin Exp Immunol
Pays: England
ID NLM: 0057202

Informations de publication

Date de publication:
05 06 2023
Historique:
received: 27 09 2022
revised: 18 01 2023
accepted: 20 02 2023
medline: 8 6 2023
pubmed: 23 2 2023
entrez: 22 2 2023
Statut: ppublish

Résumé

T cells are important in preventing severe disease from SARS-CoV-2, but scalable and field-adaptable alternatives to expert T-cell assays are needed. The interferon-gamma release assay QuantiFERON platform was developed to detect T-cell responses to SARS-CoV-2 from whole blood with relatively basic equipment and flexibility of processing timelines. Forty-eight participants with different infection and vaccination backgrounds were recruited. Whole blood samples were analysed using the QuantiFERON SARS-CoV-2 assay in parallel with the well-established 'Protective Immunity from T Cells in Healthcare workers' (PITCH) ELISpot, which can evaluate spike-specific T-cell responses. The primary aims of this cross-sectional observational cohort study were to establish if the QuantiFERON SARS-Co-V-2 assay could discern differences between specified groups and to assess the sensitivity of the assay compared with the PITCH ELISpot. The QuantiFERON SARS-CoV-2 distinguished acutely infected individuals (12-21 days post positive PCR) from naïve individuals (P < 0.0001) with 100% sensitivity and specificity for SARS-CoV-2 T cells, whilst the PITCH ELISpot had reduced sensitivity (62.5%) for the acute infection group. Sensitivity with QuantiFERON for previous infection was 12.5% (172-444 days post positive test) and was inferior to the PITCH ELISpot (75%). Although the QuantiFERON assay could discern differences between unvaccinated and vaccinated individuals (55-166 days since second vaccination), the latter also had reduced sensitivity (44.4%) compared to the PITCH ELISpot (66.6%). The QuantiFERON SARS-CoV-2 assay showed potential as a T- cell evaluation tool soon after SARS-CoV-2 infection but has lower sensitivity for use in reliable evaluation of vaccination or more distant infection.

Identifiants

pubmed: 36807499
pii: 7049390
doi: 10.1093/cei/uxad027
pmc: PMC10243914
doi:

Substances chimiques

Antibodies, Viral 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

249-261

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of the British Society for Immunology.

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Auteurs

Síle A Johnson (SA)

Peter Medawar Building for Pathogen Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.
University of Oxford Medical School, University of Oxford, Oxford, UK.
University Hospitals of Derby and Burton NHS Foundation Trust, Derby, UK.

Eloise Phillips (E)

Peter Medawar Building for Pathogen Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.

Sandra Adele (S)

Peter Medawar Building for Pathogen Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.
Oxford Centre For Global Health Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.
Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand.

Stephanie Longet (S)

Wellcome Centre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Pandemic Sciences Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.

Tom Malone (T)

Peter Medawar Building for Pathogen Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.

Chris Mason (C)

University of Oxford Medical School, University of Oxford, Oxford, UK.

Lizzie Stafford (L)

Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Department of Experimental Medicine, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.

Anni Jamsen (A)

Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Department of Experimental Medicine, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.

Siobhan Gardiner (S)

Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Department of Experimental Medicine, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.

Alexandra Deeks (A)

Peter Medawar Building for Pathogen Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.
Department of Experimental Medicine, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.

Janice Neo (J)

University Hospitals of Derby and Burton NHS Foundation Trust, Derby, UK.

Emily J Blurton (EJ)

University Hospitals of Derby and Burton NHS Foundation Trust, Derby, UK.

Jemima White (J)

University of Oxford Medical School, University of Oxford, Oxford, UK.

Muhammed Ali (M)

Peter Medawar Building for Pathogen Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.
Oxford Centre For Global Health Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.
Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand.

Barbara Kronsteiner (B)

Peter Medawar Building for Pathogen Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.
Oxford Centre For Global Health Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.

Joseph D Wilson (JD)

Peter Medawar Building for Pathogen Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.
King's College Hospital NHS Foundation Trust, London, UK.

Dónal T Skelly (DT)

Peter Medawar Building for Pathogen Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.
Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.

Katie Jeffery (K)

Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Radcliffe Department of Medicine, University of Oxford, Oxford, UK.

Christopher P Conlon (CP)

Oxford Centre For Global Health Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.
Oxford University Hospitals NHS Foundation Trust, Oxford, UK.

Philip Goulder (P)

Peter Medawar Building for Pathogen Research, Department of Paediatrics, University of Oxford, Oxford, UK.

Pitch Consortium (P)

Peter Medawar Building for Pathogen Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.

Miles Carroll (M)

Wellcome Centre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Pandemic Sciences Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.

Eleanor Barnes (E)

Peter Medawar Building for Pathogen Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.
Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, UK.
Translational Gastroenterology Unit, University of Oxford, Oxford, UK.

Paul Klenerman (P)

Peter Medawar Building for Pathogen Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.
Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, UK.
Translational Gastroenterology Unit, University of Oxford, Oxford, UK.

Susanna J Dunachie (SJ)

Peter Medawar Building for Pathogen Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.
Oxford Centre For Global Health Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.
Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand.
Oxford University Hospitals NHS Foundation Trust, Oxford, UK.

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