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Temporal Course of SARS-CoV-2 Antibody Positivity in Patients with COVID-19 following the First Clinical Presentation

Knowledge of the sensitivities of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antibody tests beyond 35 days after the clinical onset of COVID-19 is insufficient. We aimed to describe positivity rate of SARS-CoV-2 assays employing three different measurement principles over a prolong...

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Autores principales: Risch, Martin, Weber, Myriam, Thiel, Sarah, Grossmann, Kirsten, Wohlwend, Nadia, Lung, Thomas, Hillmann, Dorothea, Ritzler, Michael, Ferrara, Francesca, Bigler, Susanna, Egli, Konrad, Bodmer, Thomas, Imperiali, Mauro, Salimi, Yacir, Fleisch, Felix, Cusini, Alexia, Renz, Harald, Kohler, Philipp, Vernazza, Pietro, Kahlert, Christian R., Paprotny, Matthias, Risch, Lorenz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7673235/
https://www.ncbi.nlm.nih.gov/pubmed/33224987
http://dx.doi.org/10.1155/2020/9878453
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author Risch, Martin
Weber, Myriam
Thiel, Sarah
Grossmann, Kirsten
Wohlwend, Nadia
Lung, Thomas
Hillmann, Dorothea
Ritzler, Michael
Ferrara, Francesca
Bigler, Susanna
Egli, Konrad
Bodmer, Thomas
Imperiali, Mauro
Salimi, Yacir
Fleisch, Felix
Cusini, Alexia
Renz, Harald
Kohler, Philipp
Vernazza, Pietro
Kahlert, Christian R.
Paprotny, Matthias
Risch, Lorenz
author_facet Risch, Martin
Weber, Myriam
Thiel, Sarah
Grossmann, Kirsten
Wohlwend, Nadia
Lung, Thomas
Hillmann, Dorothea
Ritzler, Michael
Ferrara, Francesca
Bigler, Susanna
Egli, Konrad
Bodmer, Thomas
Imperiali, Mauro
Salimi, Yacir
Fleisch, Felix
Cusini, Alexia
Renz, Harald
Kohler, Philipp
Vernazza, Pietro
Kahlert, Christian R.
Paprotny, Matthias
Risch, Lorenz
author_sort Risch, Martin
collection PubMed
description Knowledge of the sensitivities of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antibody tests beyond 35 days after the clinical onset of COVID-19 is insufficient. We aimed to describe positivity rate of SARS-CoV-2 assays employing three different measurement principles over a prolonged period. Two hundred sixty-eight samples from 180 symptomatic patients with COVID-19 and a reverse transcription polymerase chain reaction (RT-PCR) test followed by serological investigation of SARS-CoV-2 antibodies were included. We conducted three chemiluminescence (including electrochemiluminescence assay (ECLIA)), four enzyme-linked immunosorbent assay (ELISA), and one lateral flow immunoassay (LFIA) test formats. Positivity rates, as well as positive (PPVs) and negative predictive values (NPVs), were calculated for each week after the first clinical presentation for COVID-19. Furthermore, combinations of tests were assessed within an orthogonal testing approach employing two independent assays and predictive values were calculated. Heat maps were constructed to graphically illustrate operational test characteristics. During a follow-up period of more than 9 weeks, chemiluminescence assays and one ELISA IgG test showed stable positivity rates after the third week. With the exception of ECLIA, the PPVs of the other chemiluminescence assays were ≥95% for COVID-19 only after the second week. ELISA and LFIA had somewhat lower PPVs. IgM exhibited insufficient predictive characteristics. An orthogonal testing approach provided PPVs ≥ 95% for patients with a moderate pretest probability (e.g., symptomatic patients), even for tests with a low single test performance. After the second week, NPVs of all but IgM assays were ≥95% for patients with low to moderate pretest probability. The confirmation of negative results using an orthogonal algorithm with another assay provided lower NPVs than the single assays. When interpreting results from SARS-CoV-2 tests, the pretest probability, time of blood draw, and assay characteristics must be carefully considered. An orthogonal testing approach increases the accuracy of positive, but not negative, predictions.
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spelling pubmed-76732352020-11-19 Temporal Course of SARS-CoV-2 Antibody Positivity in Patients with COVID-19 following the First Clinical Presentation Risch, Martin Weber, Myriam Thiel, Sarah Grossmann, Kirsten Wohlwend, Nadia Lung, Thomas Hillmann, Dorothea Ritzler, Michael Ferrara, Francesca Bigler, Susanna Egli, Konrad Bodmer, Thomas Imperiali, Mauro Salimi, Yacir Fleisch, Felix Cusini, Alexia Renz, Harald Kohler, Philipp Vernazza, Pietro Kahlert, Christian R. Paprotny, Matthias Risch, Lorenz Biomed Res Int Research Article Knowledge of the sensitivities of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antibody tests beyond 35 days after the clinical onset of COVID-19 is insufficient. We aimed to describe positivity rate of SARS-CoV-2 assays employing three different measurement principles over a prolonged period. Two hundred sixty-eight samples from 180 symptomatic patients with COVID-19 and a reverse transcription polymerase chain reaction (RT-PCR) test followed by serological investigation of SARS-CoV-2 antibodies were included. We conducted three chemiluminescence (including electrochemiluminescence assay (ECLIA)), four enzyme-linked immunosorbent assay (ELISA), and one lateral flow immunoassay (LFIA) test formats. Positivity rates, as well as positive (PPVs) and negative predictive values (NPVs), were calculated for each week after the first clinical presentation for COVID-19. Furthermore, combinations of tests were assessed within an orthogonal testing approach employing two independent assays and predictive values were calculated. Heat maps were constructed to graphically illustrate operational test characteristics. During a follow-up period of more than 9 weeks, chemiluminescence assays and one ELISA IgG test showed stable positivity rates after the third week. With the exception of ECLIA, the PPVs of the other chemiluminescence assays were ≥95% for COVID-19 only after the second week. ELISA and LFIA had somewhat lower PPVs. IgM exhibited insufficient predictive characteristics. An orthogonal testing approach provided PPVs ≥ 95% for patients with a moderate pretest probability (e.g., symptomatic patients), even for tests with a low single test performance. After the second week, NPVs of all but IgM assays were ≥95% for patients with low to moderate pretest probability. The confirmation of negative results using an orthogonal algorithm with another assay provided lower NPVs than the single assays. When interpreting results from SARS-CoV-2 tests, the pretest probability, time of blood draw, and assay characteristics must be carefully considered. An orthogonal testing approach increases the accuracy of positive, but not negative, predictions. Hindawi 2020-11-16 /pmc/articles/PMC7673235/ /pubmed/33224987 http://dx.doi.org/10.1155/2020/9878453 Text en Copyright © 2020 Martin Risch et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Risch, Martin
Weber, Myriam
Thiel, Sarah
Grossmann, Kirsten
Wohlwend, Nadia
Lung, Thomas
Hillmann, Dorothea
Ritzler, Michael
Ferrara, Francesca
Bigler, Susanna
Egli, Konrad
Bodmer, Thomas
Imperiali, Mauro
Salimi, Yacir
Fleisch, Felix
Cusini, Alexia
Renz, Harald
Kohler, Philipp
Vernazza, Pietro
Kahlert, Christian R.
Paprotny, Matthias
Risch, Lorenz
Temporal Course of SARS-CoV-2 Antibody Positivity in Patients with COVID-19 following the First Clinical Presentation
title Temporal Course of SARS-CoV-2 Antibody Positivity in Patients with COVID-19 following the First Clinical Presentation
title_full Temporal Course of SARS-CoV-2 Antibody Positivity in Patients with COVID-19 following the First Clinical Presentation
title_fullStr Temporal Course of SARS-CoV-2 Antibody Positivity in Patients with COVID-19 following the First Clinical Presentation
title_full_unstemmed Temporal Course of SARS-CoV-2 Antibody Positivity in Patients with COVID-19 following the First Clinical Presentation
title_short Temporal Course of SARS-CoV-2 Antibody Positivity in Patients with COVID-19 following the First Clinical Presentation
title_sort temporal course of sars-cov-2 antibody positivity in patients with covid-19 following the first clinical presentation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7673235/
https://www.ncbi.nlm.nih.gov/pubmed/33224987
http://dx.doi.org/10.1155/2020/9878453
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