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Detection of SARS-CoV-2 IgG Targeting Nucleocapsid or Spike Protein by Four High-Throughput Immunoassays Authorized for Emergency Use
A total of 1,200 serum samples that were tested for SARS-CoV-2 IgG antibody using the Abbott Architect immunoassay targeting the nucleocapsid protein were run in 3 SARS-CoV-2 IgG immunoassays targeting spike proteins (DiaSorin Liaison, Ortho Vitros, and Euroimmun). Consensus-positive and consensus-n...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7587121/ https://www.ncbi.nlm.nih.gov/pubmed/32817144 http://dx.doi.org/10.1128/JCM.01742-20 |
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author | Prince, Harry E. Givens, Tara S. Lapé-Nixon, Mary Clarke, Nigel J. Schwab, Dale A. Batterman, Hollis J. Jones, Robert S. Meyer, William A. Kapoor, Hema Rowland, Charles M. Haji-Sheikhi, Farnoosh Marlowe, Elizabeth M. |
author_facet | Prince, Harry E. Givens, Tara S. Lapé-Nixon, Mary Clarke, Nigel J. Schwab, Dale A. Batterman, Hollis J. Jones, Robert S. Meyer, William A. Kapoor, Hema Rowland, Charles M. Haji-Sheikhi, Farnoosh Marlowe, Elizabeth M. |
author_sort | Prince, Harry E. |
collection | PubMed |
description | A total of 1,200 serum samples that were tested for SARS-CoV-2 IgG antibody using the Abbott Architect immunoassay targeting the nucleocapsid protein were run in 3 SARS-CoV-2 IgG immunoassays targeting spike proteins (DiaSorin Liaison, Ortho Vitros, and Euroimmun). Consensus-positive and consensus-negative interpretations were defined as qualitative agreement in at least 3 of the 4 assays. Agreement of the 4 individual assays with a consensus-negative interpretation (n = 610) ranged from 96.7% to 100%, and agreement with a consensus-positive interpretation (n = 584) ranged from 94.3% to 100%. Laboratory-developed inhibition assays were utilized to evaluate 49 consensus-negative samples that were positive in only one assay; true-positive reactivity was confirmed in only 2 of these 49 (4%) samples. These findings demonstrate very high levels of agreement among 4 SARS-CoV-2 IgG assays authorized for emergency use, regardless of antigen target or assay format. Although false-positive reactivity was identified, its occurrence was rare (no more than 1.7% of samples for a given assay). |
format | Online Article Text |
id | pubmed-7587121 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-75871212020-11-06 Detection of SARS-CoV-2 IgG Targeting Nucleocapsid or Spike Protein by Four High-Throughput Immunoassays Authorized for Emergency Use Prince, Harry E. Givens, Tara S. Lapé-Nixon, Mary Clarke, Nigel J. Schwab, Dale A. Batterman, Hollis J. Jones, Robert S. Meyer, William A. Kapoor, Hema Rowland, Charles M. Haji-Sheikhi, Farnoosh Marlowe, Elizabeth M. J Clin Microbiol Immunoassays A total of 1,200 serum samples that were tested for SARS-CoV-2 IgG antibody using the Abbott Architect immunoassay targeting the nucleocapsid protein were run in 3 SARS-CoV-2 IgG immunoassays targeting spike proteins (DiaSorin Liaison, Ortho Vitros, and Euroimmun). Consensus-positive and consensus-negative interpretations were defined as qualitative agreement in at least 3 of the 4 assays. Agreement of the 4 individual assays with a consensus-negative interpretation (n = 610) ranged from 96.7% to 100%, and agreement with a consensus-positive interpretation (n = 584) ranged from 94.3% to 100%. Laboratory-developed inhibition assays were utilized to evaluate 49 consensus-negative samples that were positive in only one assay; true-positive reactivity was confirmed in only 2 of these 49 (4%) samples. These findings demonstrate very high levels of agreement among 4 SARS-CoV-2 IgG assays authorized for emergency use, regardless of antigen target or assay format. Although false-positive reactivity was identified, its occurrence was rare (no more than 1.7% of samples for a given assay). American Society for Microbiology 2020-10-21 /pmc/articles/PMC7587121/ /pubmed/32817144 http://dx.doi.org/10.1128/JCM.01742-20 Text en Copyright © 2020 American Society for Microbiology. All Rights Reserved (https://doi.org/10.1128/ASMCopyrightv2) . https://doi.org/10.1128/ASMCopyrightv2 This article is made available via the PMC Open Access Subset for unrestricted noncommercial re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Immunoassays Prince, Harry E. Givens, Tara S. Lapé-Nixon, Mary Clarke, Nigel J. Schwab, Dale A. Batterman, Hollis J. Jones, Robert S. Meyer, William A. Kapoor, Hema Rowland, Charles M. Haji-Sheikhi, Farnoosh Marlowe, Elizabeth M. Detection of SARS-CoV-2 IgG Targeting Nucleocapsid or Spike Protein by Four High-Throughput Immunoassays Authorized for Emergency Use |
title | Detection of SARS-CoV-2 IgG Targeting Nucleocapsid or Spike Protein by Four High-Throughput Immunoassays Authorized for Emergency Use |
title_full | Detection of SARS-CoV-2 IgG Targeting Nucleocapsid or Spike Protein by Four High-Throughput Immunoassays Authorized for Emergency Use |
title_fullStr | Detection of SARS-CoV-2 IgG Targeting Nucleocapsid or Spike Protein by Four High-Throughput Immunoassays Authorized for Emergency Use |
title_full_unstemmed | Detection of SARS-CoV-2 IgG Targeting Nucleocapsid or Spike Protein by Four High-Throughput Immunoassays Authorized for Emergency Use |
title_short | Detection of SARS-CoV-2 IgG Targeting Nucleocapsid or Spike Protein by Four High-Throughput Immunoassays Authorized for Emergency Use |
title_sort | detection of sars-cov-2 igg targeting nucleocapsid or spike protein by four high-throughput immunoassays authorized for emergency use |
topic | Immunoassays |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7587121/ https://www.ncbi.nlm.nih.gov/pubmed/32817144 http://dx.doi.org/10.1128/JCM.01742-20 |
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