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Performance evaluation of serological assays to determine the immunoglobulin status in SARS-CoV-2 infected patients

BACKGROUND: Serological assays for the determination of the immune status of patients that have tested positive for infection with SARS-CoV-2 by RT-PCR are required for, e.g., contact tracing and epidemiological studies. However, data concerning the performance parameters of commercially available h...

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Autores principales: Wechselberger, Christian, Süßner, Susanne, Doppler, Stefan, Bernhard, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Author(s). Published by Elsevier B.V. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7417972/
https://www.ncbi.nlm.nih.gov/pubmed/32810840
http://dx.doi.org/10.1016/j.jcv.2020.104589
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author Wechselberger, Christian
Süßner, Susanne
Doppler, Stefan
Bernhard, David
author_facet Wechselberger, Christian
Süßner, Susanne
Doppler, Stefan
Bernhard, David
author_sort Wechselberger, Christian
collection PubMed
description BACKGROUND: Serological assays for the determination of the immune status of patients that have tested positive for infection with SARS-CoV-2 by RT-PCR are required for, e.g., contact tracing and epidemiological studies. However, data concerning the performance parameters of commercially available high-throughput ELISA tests are still not available on a large scale. STUDY DESIGN: In our study, we have evaluated an in-house developed ELISA for the detection of the immunoglobulin classes A, G and M directed against the full-length spike glycoprotein from SARS-CoV-2. For this analysis, we have included 110 sera from patients presenting with COVID-19 symptoms or blood donors without symptoms collected at the Austrian Red Cross, Blood Transfusion Service for Upper Austria, Linz. In addition, we have selected four commercially available IgG-based ELISAs as well as one IgA/IgG-based ELISA for the detection of SARS-CoV-2 antigens as well as a multiplexed IgG-based micro-ELISA assay developed for rapid Point of Care testing applications. CONCLUSIONS: All assays evaluated in the course of this study demonstrated suitable sensitivity and specificity values for the identification of patients that have experienced a past infection with SARS-CoV-2. However, testing for the presence of additional immunoglobulins (IgA and IgM) as well as using combinations of different viral antigens is highly advised to improve the predictive values of serological assays.
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spelling pubmed-74179722020-08-11 Performance evaluation of serological assays to determine the immunoglobulin status in SARS-CoV-2 infected patients Wechselberger, Christian Süßner, Susanne Doppler, Stefan Bernhard, David J Clin Virol Article BACKGROUND: Serological assays for the determination of the immune status of patients that have tested positive for infection with SARS-CoV-2 by RT-PCR are required for, e.g., contact tracing and epidemiological studies. However, data concerning the performance parameters of commercially available high-throughput ELISA tests are still not available on a large scale. STUDY DESIGN: In our study, we have evaluated an in-house developed ELISA for the detection of the immunoglobulin classes A, G and M directed against the full-length spike glycoprotein from SARS-CoV-2. For this analysis, we have included 110 sera from patients presenting with COVID-19 symptoms or blood donors without symptoms collected at the Austrian Red Cross, Blood Transfusion Service for Upper Austria, Linz. In addition, we have selected four commercially available IgG-based ELISAs as well as one IgA/IgG-based ELISA for the detection of SARS-CoV-2 antigens as well as a multiplexed IgG-based micro-ELISA assay developed for rapid Point of Care testing applications. CONCLUSIONS: All assays evaluated in the course of this study demonstrated suitable sensitivity and specificity values for the identification of patients that have experienced a past infection with SARS-CoV-2. However, testing for the presence of additional immunoglobulins (IgA and IgM) as well as using combinations of different viral antigens is highly advised to improve the predictive values of serological assays. The Author(s). Published by Elsevier B.V. 2020-10 2020-08-11 /pmc/articles/PMC7417972/ /pubmed/32810840 http://dx.doi.org/10.1016/j.jcv.2020.104589 Text en © 2020 The Authors 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
Wechselberger, Christian
Süßner, Susanne
Doppler, Stefan
Bernhard, David
Performance evaluation of serological assays to determine the immunoglobulin status in SARS-CoV-2 infected patients
title Performance evaluation of serological assays to determine the immunoglobulin status in SARS-CoV-2 infected patients
title_full Performance evaluation of serological assays to determine the immunoglobulin status in SARS-CoV-2 infected patients
title_fullStr Performance evaluation of serological assays to determine the immunoglobulin status in SARS-CoV-2 infected patients
title_full_unstemmed Performance evaluation of serological assays to determine the immunoglobulin status in SARS-CoV-2 infected patients
title_short Performance evaluation of serological assays to determine the immunoglobulin status in SARS-CoV-2 infected patients
title_sort performance evaluation of serological assays to determine the immunoglobulin status in sars-cov-2 infected patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7417972/
https://www.ncbi.nlm.nih.gov/pubmed/32810840
http://dx.doi.org/10.1016/j.jcv.2020.104589
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