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Design and performance characteristics of the Elecsys anti-SARS-CoV-2 S assay
BACKGROUND: Automated, high throughput assays are required to quantify the immune response after infection with or vaccination against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). This study on the Roche Elecsys(®) Anti-SARS-CoV-2 S (ACOV2S) assay provides insights on the assay desi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9756759/ https://www.ncbi.nlm.nih.gov/pubmed/36532081 http://dx.doi.org/10.3389/fimmu.2022.1002576 |
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author | Taffertshofer, Karin Walter, Mirko Mackeben, Peter Kraemer, Julia Potapov, Sergej Jochum, Simon |
author_facet | Taffertshofer, Karin Walter, Mirko Mackeben, Peter Kraemer, Julia Potapov, Sergej Jochum, Simon |
author_sort | Taffertshofer, Karin |
collection | PubMed |
description | BACKGROUND: Automated, high throughput assays are required to quantify the immune response after infection with or vaccination against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). This study on the Roche Elecsys(®) Anti-SARS-CoV-2 S (ACOV2S) assay provides insights on the assay design and performance. METHODS: The ACOV2S assay quantifies antibodies to the receptor-binding domain of the SARS-CoV-2 spike protein. The assigned units and the underlying standardization were compared to the international reference standard in BAU/mL. Assay specificity was assessed in samples (n=5981) collected prior to the COVID-19 pandemic and in samples from patients with non-COVID-19 respiratory infections (n=697) or other infectious diseases (n=771). Sensitivity was measured in 1313 samples from patients with mild COVID-19 and 297 samples from patients hospitalized with COVID-19. Comparison of results was performed to a comparator semi-quantitative anti-S1 assay of indirect detection format as well as a commercially available and an in-house version of a surrogate neutralization assay (ACE2-RBD). RESULTS: The originally assigned units for the ACOV2S assay were shown to be congruent to the units of the First International WHO Standard for anti-SARS-CoV-2 immunoglobulins. Overall specificity was 99.98% with no geographical differences noted and no loss of specificity in samples containing potentially cross-reacting antibodies. High sensitivity was observed, with 98.8% of samples reported to be reactive >14 days after infection and sustained detection of antibodies over time. For all samples, ACOV2S titers and neutralization capacities developed with comparable dynamics. Robust standardization and assay setup enable excellent reproducibility of results, independent of lot or analyzer used. CONCLUSION: The results from this study confirmed that ACOV2S is a highly sensitive and specific assay and correlates well with surrogate neutralization assays. The units established for ACOV2S are also interchangeable with the units of the First International WHO Standard for anti-SARS-CoV-2 immunoglobulins. Worldwide availability of the assay and analyzers render ACOV2S a highly practical tool for population-wide assessment and monitoring of the humoral response to SARS-CoV-2 infection or vaccination. |
format | Online Article Text |
id | pubmed-9756759 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97567592022-12-17 Design and performance characteristics of the Elecsys anti-SARS-CoV-2 S assay Taffertshofer, Karin Walter, Mirko Mackeben, Peter Kraemer, Julia Potapov, Sergej Jochum, Simon Front Immunol Immunology BACKGROUND: Automated, high throughput assays are required to quantify the immune response after infection with or vaccination against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). This study on the Roche Elecsys(®) Anti-SARS-CoV-2 S (ACOV2S) assay provides insights on the assay design and performance. METHODS: The ACOV2S assay quantifies antibodies to the receptor-binding domain of the SARS-CoV-2 spike protein. The assigned units and the underlying standardization were compared to the international reference standard in BAU/mL. Assay specificity was assessed in samples (n=5981) collected prior to the COVID-19 pandemic and in samples from patients with non-COVID-19 respiratory infections (n=697) or other infectious diseases (n=771). Sensitivity was measured in 1313 samples from patients with mild COVID-19 and 297 samples from patients hospitalized with COVID-19. Comparison of results was performed to a comparator semi-quantitative anti-S1 assay of indirect detection format as well as a commercially available and an in-house version of a surrogate neutralization assay (ACE2-RBD). RESULTS: The originally assigned units for the ACOV2S assay were shown to be congruent to the units of the First International WHO Standard for anti-SARS-CoV-2 immunoglobulins. Overall specificity was 99.98% with no geographical differences noted and no loss of specificity in samples containing potentially cross-reacting antibodies. High sensitivity was observed, with 98.8% of samples reported to be reactive >14 days after infection and sustained detection of antibodies over time. For all samples, ACOV2S titers and neutralization capacities developed with comparable dynamics. Robust standardization and assay setup enable excellent reproducibility of results, independent of lot or analyzer used. CONCLUSION: The results from this study confirmed that ACOV2S is a highly sensitive and specific assay and correlates well with surrogate neutralization assays. The units established for ACOV2S are also interchangeable with the units of the First International WHO Standard for anti-SARS-CoV-2 immunoglobulins. Worldwide availability of the assay and analyzers render ACOV2S a highly practical tool for population-wide assessment and monitoring of the humoral response to SARS-CoV-2 infection or vaccination. Frontiers Media S.A. 2022-12-02 /pmc/articles/PMC9756759/ /pubmed/36532081 http://dx.doi.org/10.3389/fimmu.2022.1002576 Text en Copyright © 2022 Taffertshofer, Walter, Mackeben, Kraemer, Potapov and Jochum https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Taffertshofer, Karin Walter, Mirko Mackeben, Peter Kraemer, Julia Potapov, Sergej Jochum, Simon Design and performance characteristics of the Elecsys anti-SARS-CoV-2 S assay |
title | Design and performance characteristics of the Elecsys anti-SARS-CoV-2 S assay |
title_full | Design and performance characteristics of the Elecsys anti-SARS-CoV-2 S assay |
title_fullStr | Design and performance characteristics of the Elecsys anti-SARS-CoV-2 S assay |
title_full_unstemmed | Design and performance characteristics of the Elecsys anti-SARS-CoV-2 S assay |
title_short | Design and performance characteristics of the Elecsys anti-SARS-CoV-2 S assay |
title_sort | design and performance characteristics of the elecsys anti-sars-cov-2 s assay |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9756759/ https://www.ncbi.nlm.nih.gov/pubmed/36532081 http://dx.doi.org/10.3389/fimmu.2022.1002576 |
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