Convalescent plasma therapy for the treatment of patients with COVID-19: Assessment of methods available for antibody detection and their correlation with neutralising antibody levels.


Journal

Transfusion medicine (Oxford, England)
ISSN: 1365-3148
Titre abrégé: Transfus Med
Pays: England
ID NLM: 9301182

Informations de publication

Date de publication:
Jun 2021
Historique:
revised: 30 09 2020
received: 17 08 2020
accepted: 02 10 2020
pubmed: 18 12 2020
medline: 17 6 2021
entrez: 17 12 2020
Statut: ppublish

Résumé

The lack of approved specific therapeutic agents to treat coronavirus disease (COVID-19) associated with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection has led to the rapid implementation of convalescent plasma therapy (CPT) trials in many countries, including the United Kingdom. Effective CPT is likely to require high titres of neutralising antibody (nAb) in convalescent donations. Understanding the relationship between functional neutralising antibodies and antibody levels to specific SARS-CoV-2 proteins in scalable assays will be crucial for the success of a large-scale collection. We assessed whether neutralising antibody titres correlated with reactivity in a range of enzyme-linked immunosorbent assays (ELISA) targeting the spike (S) protein, the main target for human immune response. Blood samples were collected from 52 individuals with a previous laboratory-confirmed SARS-CoV-2 infection. These were assayed for SARS-CoV-2 nAbs by microneutralisation and pseudo-type assays and for antibodies by four different ELISAs. Receiver operating characteristic (ROC) analysis was used to further identify sensitivity and specificity of selected assays to identify samples containing high nAb levels. All samples contained SARS-CoV-2 antibodies, whereas neutralising antibody titres of greater than 1:20 were detected in 43 samples (83% of those tested) and >1:100 in 22 samples (42%). The best correlations were observed with EUROimmun immunoglobulin G (IgG) reactivity (Spearman Rho correlation coefficient 0.88; p < 0.001). Based on ROC analysis, EUROimmun would detect 60% of samples with titres of >1:100 with 100% specificity using a reactivity index of 9.1 (13/22). Robust associations between nAb titres and reactivity in several ELISA-based antibody tests demonstrate their possible utility for scaled-up production of convalescent plasma containing potentially therapeutic levels of anti-SARS-CoV-2 nAbs.

Identifiants

pubmed: 33333627
doi: 10.1111/tme.12746
pmc: PMC8246874
doi:

Substances chimiques

Antibodies, Neutralizing 0
Antibodies, Viral 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

167-175

Subventions

Organisme : Public Health England
Organisme : Department of Health and Social Care (DHSC)/UKRI/NIHR COVID-19 Rapid Response Grant (COV19-RECPLA)
Organisme : European Research Council
ID : 812816
Pays : International

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2020 The Authors. Transfusion Medicine published by John Wiley & Sons Ltd on behalf of British Blood Transfusion Society.

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Auteurs

Heli Harvala (H)

National Microbiology Services, NHS Blood and Transplant, London, UK.

Matthew L Robb (ML)

Statistics and Clinical Studies, NHS Blood and Transplant, Bristol, UK.

Nick Watkins (N)

Department of Research and Development, NHS Blood and Transplant Cambridge, Cambridge, UK.

Samreen Ijaz (S)

Virology Reference Department, National Infection Service, Public Health England, London, UK.

Steven Dicks (S)

Virology Reference Department, National Infection Service, Public Health England, London, UK.

Monika Patel (M)

High Containment Microbiology, National Infection Service, Public Health England, London, UK.

Piyada Supasa (P)

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

Dejnirattisai Wanwisa (D)

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

Chang Liu (C)

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

Juthathip Mongkolsapaya (J)

Wellcome Centre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Dengue Hemorrhagic Fever Research Unit, Office for Research and Development, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand.

Abbie Bown (A)

Rare and Imported Pathogens Laboratory, Public Health England, Porton Down, Wiltshire, UK.

Daniel Bailey (D)

Rare and Imported Pathogens Laboratory, Public Health England, Porton Down, Wiltshire, UK.

Richard Vipond (R)

Rare and Imported Pathogens Laboratory, Public Health England, Porton Down, Wiltshire, UK.

Nicholas Grayson (N)

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

Nigel Temperton (N)

Medway School of Pharmacy, University of Kent, Chatham, UK.

Sunetra Gupta (S)

Department of Zoology, University of Oxford, Oxford, UK.

Rutger J Ploeg (RJ)

Nuffield Department of Surgical Sciences, University of Oxford, Oxford, UK.
Department of Transplant Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.

Jai Bolton (J)

Department of Zoology, University of Oxford, Oxford, UK.

Alex Fyfe (A)

Department of Zoology, University of Oxford, Oxford, UK.

Robin Gopal (R)

Virology Reference Department, National Infection Service, Public Health England, London, UK.

Peter Simmonds (P)

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

Gavin Screaton (G)

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

Craig Thompson (C)

Department of Zoology, University of Oxford, Oxford, UK.

Tim Brooks (T)

Rare and Imported Pathogens Laboratory, Public Health England, Porton Down, Wiltshire, UK.

Maria Zambon (M)

Virology Reference Department, National Infection Service, Public Health England, London, UK.

Gail Miflin (G)

Department of Chief Medical Officer, NHS Blood and Transplant, Bristol, UK.

David J Roberts (DJ)

NHS Blood and Transplant, Oxford, John Radcliffe Hospital, Oxford, UK.
Radcliffe Department of Medicine and BRC Haematology Theme, University of Oxford, John Radcliffe Hospital, Oxford, UK.

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