SARS Antibody Testing in Children: Development of Oral Fluid Assays for IgG Measurements.


Journal

Microbiology spectrum
ISSN: 2165-0497
Titre abrégé: Microbiol Spectr
Pays: United States
ID NLM: 101634614

Informations de publication

Date de publication:
23 02 2022
Historique:
pubmed: 6 1 2022
medline: 22 3 2022
entrez: 5 1 2022
Statut: ppublish

Résumé

Seroepidemiological studies to monitor antibody kinetics are important for assessing the extent and spread of SARS-CoV-2 in a population. Noninvasive sampling methods are advantageous for reducing the need for venipuncture, which may be a barrier to investigations, particularly in pediatric populations. Oral fluids are obtained by gingiva-crevicular sampling from children and adults and are very well accepted. Enzyme immunoassays (EIAs) based on these samples have acceptable sensitivity and specificity compared to conventional serum-based antibody EIAs and are suitable for population-based surveillance. We describe the development and evaluation of SARS-CoV-2 IgG EIAs using SARS-CoV-2 viral nucleoprotein (NP) and spike (S) proteins in IgG isotype capture format and an indirect receptor-binding-domain (RBD) IgG EIA, intended for use in children as a primary endpoint. All three assays were assessed using a panel of 1,999 paired serum and oral fluids from children and adults participating in school SARS-CoV-2 surveillance studies during and after the first and second pandemic wave in the United Kingdom. The anti-NP IgG capture assay was the best candidate, with an overall sensitivity of 75% (95% confidence interval [CI]: 71 to 79%) and specificity of 99% (95% CI: 78 to 99%) compared with paired serum antibodies. Sensitivity observed in children (80%, 95% CI: 71 to 88%) was higher than that in adults (67%, CI: 60% to 74%). Oral fluid assays (OF) using spike protein and RBD antigens were also 99% specific and achieved reasonable but lower sensitivity in the target population (78%, 95% CI [68% to 86%] and 53%, 95% CI [43% to 64%], respectively).

Identifiants

pubmed: 34985331
doi: 10.1128/spectrum.00786-21
pmc: PMC8729769
doi:

Substances chimiques

Antibodies, Viral 0
Immunoglobulin G 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0078621

Subventions

Organisme : Department of Health
Pays : United Kingdom

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Auteurs

Katja Hoschler (K)

Virus Reference Department, Public Health Englandgrid.271308.f, London, United Kingdom.

Samreen Ijaz (S)

Virus Reference Department, Public Health Englandgrid.271308.f, London, United Kingdom.

Nick Andrews (N)

Immunisation and Countermeasures Division, Public Health Englandgrid.271308.f, London, United Kingdom.

Sammy Ho (S)

Virus Reference Department, Public Health Englandgrid.271308.f, London, United Kingdom.

Steve Dicks (S)

Virus Reference Department, Public Health Englandgrid.271308.f, London, United Kingdom.
Microbiology Services Laboratory, NHS Blood and Transplant, Bristol, United Kingdom.

Keerthana Jegatheesan (K)

Virus Reference Department, Public Health Englandgrid.271308.f, London, United Kingdom.
Microbiology Services Laboratory, NHS Blood and Transplant, Bristol, United Kingdom.

John Poh (J)

Virus Reference Department, Public Health Englandgrid.271308.f, London, United Kingdom.

Lenesha Warrener (L)

Virus Reference Department, Public Health Englandgrid.271308.f, London, United Kingdom.

Thivya Kankeyan (T)

Virus Reference Department, Public Health Englandgrid.271308.f, London, United Kingdom.

Frances Baawuah (F)

Immunisation and Countermeasures Division, Public Health Englandgrid.271308.f, London, United Kingdom.

Joanne Beckmann (J)

East London NHS Foundation Trustgrid.450709.f, London, United Kingdom.

Ifeanichukwu O Okike (IO)

Derbyshire Healthcare NHS Foundation Trust, Derby, United Kingdom.

Shazaad Ahmad (S)

Manchester University NHS Foundation Trust, Manchester, United Kingdom.

Joanna Garstang (J)

Birmingham Community Healthcare NHS Trustgrid.439530.8, Aston, United Kingdom.

Andrew J Brent (AJ)

Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.
University of Oxford, Oxford, United Kingdom.

Bernadette Brent (B)

Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.
University of Oxford, Oxford, United Kingdom.

Felicity Aiano (F)

Immunisation and Countermeasures Division, Public Health Englandgrid.271308.f, London, United Kingdom.

Kevin E Brown (KE)

Immunisation and Countermeasures Division, Public Health Englandgrid.271308.f, London, United Kingdom.

Mary E Ramsay (ME)

Immunisation and Countermeasures Division, Public Health Englandgrid.271308.f, London, United Kingdom.

David Brown (D)

Virus Reference Department, Public Health Englandgrid.271308.f, London, United Kingdom.
Fundação Oswaldo Cruz-Fiocruz, Instituto Oswaldo Cruz, Laboratório de Vírus Respiratórios e do Sarampo, Rio de Janeiro, Rio de Janeiro, Brasil.

John V Parry (JV)

Virus Reference Department, Public Health Englandgrid.271308.f, London, United Kingdom.

Shamez N Ladhani (SN)

Immunisation and Countermeasures Division, Public Health Englandgrid.271308.f, London, United Kingdom.
Paediatric Infectious Diseases Research Group, St. George's University of London, London, United Kingdom.

Maria Zambon (M)

Virus Reference Department, Public Health Englandgrid.271308.f, London, United Kingdom.

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