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A novel multiplex electrochemiluminescent immunoassay for detection and quantification of anti-SARS-CoV-2 IgG and anti-seasonal endemic human coronavirus IgG

BACKGROUND: Multiplex immunoassays capture a comprehensive profile of the humoral response against SARS-CoV-2 and human endemic coronaviruses. We validated a multiplex panel (V-PLEX Panel 2) from Meso Scale Diagnostics targeting antibodies against nine coronavirus antigens. Performance was compared...

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Autores principales: Li, Fang Fang, Liu, Aaron, Gibbs, Ebrima, Tanunliong, Guadalein, Marquez, Ana Citlali, Gantt, Soren, Frykman, Hans, Krajden, Mel, Morshed, Muhammad, Prystajecky, Natalie A., Cashman, Neil, Sekirov, Inna, Jassem, Agatha N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. Published by Elsevier B.V. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8632860/
https://www.ncbi.nlm.nih.gov/pubmed/34883405
http://dx.doi.org/10.1016/j.jcv.2021.105050
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author Li, Fang Fang
Liu, Aaron
Gibbs, Ebrima
Tanunliong, Guadalein
Marquez, Ana Citlali
Gantt, Soren
Frykman, Hans
Krajden, Mel
Morshed, Muhammad
Prystajecky, Natalie A.
Cashman, Neil
Sekirov, Inna
Jassem, Agatha N.
author_facet Li, Fang Fang
Liu, Aaron
Gibbs, Ebrima
Tanunliong, Guadalein
Marquez, Ana Citlali
Gantt, Soren
Frykman, Hans
Krajden, Mel
Morshed, Muhammad
Prystajecky, Natalie A.
Cashman, Neil
Sekirov, Inna
Jassem, Agatha N.
author_sort Li, Fang Fang
collection PubMed
description BACKGROUND: Multiplex immunoassays capture a comprehensive profile of the humoral response against SARS-CoV-2 and human endemic coronaviruses. We validated a multiplex panel (V-PLEX Panel 2) from Meso Scale Diagnostics targeting antibodies against nine coronavirus antigens. Performance was compared against alternative single- and multi-antigen immunoassays. METHODS: Sera collected for clinical or public health testing from 2018 to 2020 (n = 135) were used to compare all tested platforms, and inter-test agreement was assessed by Cohen's kappa coefficient. Sample category (positive/negative) was assigned based on collection date relative to the index case in Canada, and SARS-CoV-2 PCR and serology results. 117 out of the 135 samples (31 positive, 86 negative) were assigned a category and were used to calculate sensitivity and specificity, with MSD's test results based upon manufacturer-set cut-offs. RESULTS: We observed SARS-CoV-2 target sensitivities of 100% and specificities >94% for all antigens (RBD, Nucleocapsid, Spike) in V-PLEX Panel 2. When targets were combined, we found a SARS-CoV-2 sensitivity of 100% and specificity of 98.8% with no difference in performance compared to clinical assays, and Cohen's kappa ranging from 0.798 to 0.945 compared to surface plasmon resonance imaging (SPRi). Quantitative measurements of antibodies against the Spike protein of endemic human coronaviruses were concordant with SPRi. CONCLUSION: Meso Scale Diagnostics’ V-PLEX Coronavirus Panel 2 allows for highly sensitive and specific detection of anti-coronavirus IgG, and is concordant with other serological assays for detection of antibodies against SARS-CoV-2 and the endemic human coronaviruses, making it a good tool for humoral response characterization after both infection and vaccination.
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spelling pubmed-86328602021-12-01 A novel multiplex electrochemiluminescent immunoassay for detection and quantification of anti-SARS-CoV-2 IgG and anti-seasonal endemic human coronavirus IgG Li, Fang Fang Liu, Aaron Gibbs, Ebrima Tanunliong, Guadalein Marquez, Ana Citlali Gantt, Soren Frykman, Hans Krajden, Mel Morshed, Muhammad Prystajecky, Natalie A. Cashman, Neil Sekirov, Inna Jassem, Agatha N. J Clin Virol Article BACKGROUND: Multiplex immunoassays capture a comprehensive profile of the humoral response against SARS-CoV-2 and human endemic coronaviruses. We validated a multiplex panel (V-PLEX Panel 2) from Meso Scale Diagnostics targeting antibodies against nine coronavirus antigens. Performance was compared against alternative single- and multi-antigen immunoassays. METHODS: Sera collected for clinical or public health testing from 2018 to 2020 (n = 135) were used to compare all tested platforms, and inter-test agreement was assessed by Cohen's kappa coefficient. Sample category (positive/negative) was assigned based on collection date relative to the index case in Canada, and SARS-CoV-2 PCR and serology results. 117 out of the 135 samples (31 positive, 86 negative) were assigned a category and were used to calculate sensitivity and specificity, with MSD's test results based upon manufacturer-set cut-offs. RESULTS: We observed SARS-CoV-2 target sensitivities of 100% and specificities >94% for all antigens (RBD, Nucleocapsid, Spike) in V-PLEX Panel 2. When targets were combined, we found a SARS-CoV-2 sensitivity of 100% and specificity of 98.8% with no difference in performance compared to clinical assays, and Cohen's kappa ranging from 0.798 to 0.945 compared to surface plasmon resonance imaging (SPRi). Quantitative measurements of antibodies against the Spike protein of endemic human coronaviruses were concordant with SPRi. CONCLUSION: Meso Scale Diagnostics’ V-PLEX Coronavirus Panel 2 allows for highly sensitive and specific detection of anti-coronavirus IgG, and is concordant with other serological assays for detection of antibodies against SARS-CoV-2 and the endemic human coronaviruses, making it a good tool for humoral response characterization after both infection and vaccination. The Authors. Published by Elsevier B.V. 2022-01 2021-12-01 /pmc/articles/PMC8632860/ /pubmed/34883405 http://dx.doi.org/10.1016/j.jcv.2021.105050 Text en © 2021 The Authors. Published by Elsevier B.V. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Li, Fang Fang
Liu, Aaron
Gibbs, Ebrima
Tanunliong, Guadalein
Marquez, Ana Citlali
Gantt, Soren
Frykman, Hans
Krajden, Mel
Morshed, Muhammad
Prystajecky, Natalie A.
Cashman, Neil
Sekirov, Inna
Jassem, Agatha N.
A novel multiplex electrochemiluminescent immunoassay for detection and quantification of anti-SARS-CoV-2 IgG and anti-seasonal endemic human coronavirus IgG
title A novel multiplex electrochemiluminescent immunoassay for detection and quantification of anti-SARS-CoV-2 IgG and anti-seasonal endemic human coronavirus IgG
title_full A novel multiplex electrochemiluminescent immunoassay for detection and quantification of anti-SARS-CoV-2 IgG and anti-seasonal endemic human coronavirus IgG
title_fullStr A novel multiplex electrochemiluminescent immunoassay for detection and quantification of anti-SARS-CoV-2 IgG and anti-seasonal endemic human coronavirus IgG
title_full_unstemmed A novel multiplex electrochemiluminescent immunoassay for detection and quantification of anti-SARS-CoV-2 IgG and anti-seasonal endemic human coronavirus IgG
title_short A novel multiplex electrochemiluminescent immunoassay for detection and quantification of anti-SARS-CoV-2 IgG and anti-seasonal endemic human coronavirus IgG
title_sort novel multiplex electrochemiluminescent immunoassay for detection and quantification of anti-sars-cov-2 igg and anti-seasonal endemic human coronavirus igg
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8632860/
https://www.ncbi.nlm.nih.gov/pubmed/34883405
http://dx.doi.org/10.1016/j.jcv.2021.105050
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