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

Abstract:
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.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1093/cei/uxad027

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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-4100-8522
More by this author
Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-5641-6369
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0003-4458-1751
More by this author
Institution:
University of Oxford
Role:
Author
More by this author
Institution:
University of Oxford
Role:
Author


Publisher:
Oxford University Press
Journal:
Clinical & Experimental Immunology More from this journal
Volume:
212
Issue:
3
Pages:
249-261
Publication date:
2023-02-21
Acceptance date:
2023-02-20
DOI:
EISSN:
1365-2249
ISSN:
0009-9104


Language:
English
Keywords:
Pubs id:
1330567
Local pid:
pubs:1330567
Source identifiers:
W4321436155
Deposit date:
2026-08-07
ARK identifier:
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