Harmonization and qualification of an IFN-γ Enzyme-Linked ImmunoSpot assay (ELISPOT) to measure influenza-specific cell-mediated immunity within the FLUCOP consortium.


Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2022
Historique:
received: 02 07 2022
accepted: 08 08 2022
entrez: 26 9 2022
pubmed: 27 9 2022
medline: 28 9 2022
Statut: epublish

Résumé

Influenza continues to be the most important cause of viral respiratory disease, despite the availability of vaccines. Today's evaluation of influenza vaccines mainly focuses on the quantitative and functional analyses of antibodies to the surface proteins haemagglutinin (HA) and neuraminidase (NA). However, there is an increasing interest in measuring cellular immune responses targeting not only mutation-prone surface HA and NA but also conserved internal proteins as these are less explored yet potential correlates of protection. To date, laboratories that monitor cellular immune responses use a variety of in-house procedures. This generates diverging results, complicates interlaboratory comparisons, and hampers influenza vaccine evaluation. The European FLUCOP project aims to develop and standardize assays for the assessment of influenza vaccine correlates of protection. This report describes the harmonization and qualification of the influenza-specific interferon-gamma (IFN-γ) Enzyme-Linked ImmunoSpot (ELISpot) assay. Initially, two pilot studies were conducted to identify sources of variability during sample analysis and spot enumeration in order to develop a harmonized Standard Operating Procedure (SOP). Subsequently, an assay qualification study was performed to investigate the linearity, intermediate precision (reproducibility), repeatability, specificity, Lower and Upper Limits of Quantification (LLOQ-ULOQ), Limit of Detection (LOD) and the stability of signal over time. We were able to demonstrate that the FLUCOP harmonized IFN-γ ELISpot assay procedure can accurately enumerate IFN-γ secreting cells in the analytical range of 34.4 Spot Forming Units (SFU) per million cells up to the technical limit of the used reader and in the linear range from 120 000 to 360 000 cells per well, in plates stored up to 6 weeks after development. This IFN-γ ELISpot procedure will hopefully become a useful and reliable tool to investigate influenza-specific cellular immune responses induced by natural infection or vaccination and can be an additional instrument in the search for novel correlates of protection.

Identifiants

pubmed: 36159843
doi: 10.3389/fimmu.2022.984642
pmc: PMC9493492
doi:

Substances chimiques

Hemagglutinins 0
Influenza Vaccines 0
Membrane Proteins 0
Interferon-gamma 82115-62-6
Neuraminidase EC 3.2.1.18

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

984642

Informations de copyright

Copyright © 2022 Waerlop, Leroux-Roels, Lambe, Bellamy, Medaglini, Pettini, Cox, Trieu, Davies, Bredholt, Montomoli, Gianchecchi and Clement.

Déclaration de conflit d'intérêts

Authors EM and EG are employed by VisMederi srl. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Gwenn Waerlop (G)

Center for Vaccinology (CEVAC), University Hospital, Ghent University, Ghent, Belgium.

Geert Leroux-Roels (G)

Center for Vaccinology (CEVAC), University Hospital, Ghent University, Ghent, Belgium.

Teresa Lambe (T)

Nuffield Department of Medicine, The Jenner Institute, University of Oxford, Oxford, United Kingdom.

Duncan Bellamy (D)

Nuffield Department of Medicine, The Jenner Institute, University of Oxford, Oxford, United Kingdom.

Donata Medaglini (D)

Laboratory of Molecular Microbiology and Biotechnology, Department of Medical Biotechnologies, University of Siena, Siena, Italy.

Elena Pettini (E)

Laboratory of Molecular Microbiology and Biotechnology, Department of Medical Biotechnologies, University of Siena, Siena, Italy.

Rebecca Jane Cox (RJ)

Influenza Centre, Department of Clinical Science, University of Bergen, Bergen, Norway.

Mai-Chi Trieu (MC)

Influenza Centre, Department of Clinical Science, University of Bergen, Bergen, Norway.

Richard Davies (R)

Influenza Centre, Department of Clinical Science, University of Bergen, Bergen, Norway.

Geir Bredholt (G)

Influenza Centre, Department of Clinical Science, University of Bergen, Bergen, Norway.

Emanuele Montomoli (E)

Department of Molecular and Developmental Medicine, University of Siena, Siena, Italy.
VisMederi srl, Siena, Italy.

Elena Gianchecchi (E)

VisMederi srl, Siena, Italy.

Frédéric Clement (F)

Center for Vaccinology (CEVAC), University Hospital, Ghent University, Ghent, Belgium.

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