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Clinical evaluation of the antibody response in patients with COVID-19 using automated high-throughput immunoassays
Several automated high-throughput immunoassays for detecting anti-SARS-CoV-2 antibodies by a semi-quantitative approach have been commercialized. In this study, we describe the timeline of the antibody response in patients with RT-PCR-confirmed COVID-19. A total of 292 sequential serum samples from...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7954771/ https://www.ncbi.nlm.nih.gov/pubmed/33744623 http://dx.doi.org/10.1016/j.diagmicrobio.2021.115370 |
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author | Kubota, Katsumi Kitagawa, Yutaro Matsuoka, Masaru Imai, Kazuo Orihara, Yuta Kawamura, Rieko Sakai, Jun Ishibashi, Noriomi Tarumoto, Norihito Takeuchi, Shinichi Maesaki, Shigefumi Maeda, Takuya |
author_facet | Kubota, Katsumi Kitagawa, Yutaro Matsuoka, Masaru Imai, Kazuo Orihara, Yuta Kawamura, Rieko Sakai, Jun Ishibashi, Noriomi Tarumoto, Norihito Takeuchi, Shinichi Maesaki, Shigefumi Maeda, Takuya |
author_sort | Kubota, Katsumi |
collection | PubMed |
description | Several automated high-throughput immunoassays for detecting anti-SARS-CoV-2 antibodies by a semi-quantitative approach have been commercialized. In this study, we describe the timeline of the antibody response in patients with RT-PCR-confirmed COVID-19. A total of 292 sequential serum samples from 33 Japanese patients were retrospectively analyzed using four test kits for SARS-CoV-2: the Abbott SARS-CoV-2 IgG assay (Abbott), Elecsys® Anti-SARS-CoV-2 assay (Roche Diagnostic), and VITROS® Anti-SARS-CoV-2 Total and IgG assays (Ortho Clinical Diagnostics). All automated immunoassays could equivalently identify positive sera collected within 2 weeks after symptom onset (99.3%–100%). In addition, the S protein-based automated immunoassay, the VITROS® Anti-SARS-CoV-2 Total assay, may play a complementary role in evaluating passive antibody therapies or vaccines against SARS-CoV-2, although further research is required. |
format | Online Article Text |
id | pubmed-7954771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79547712021-03-15 Clinical evaluation of the antibody response in patients with COVID-19 using automated high-throughput immunoassays Kubota, Katsumi Kitagawa, Yutaro Matsuoka, Masaru Imai, Kazuo Orihara, Yuta Kawamura, Rieko Sakai, Jun Ishibashi, Noriomi Tarumoto, Norihito Takeuchi, Shinichi Maesaki, Shigefumi Maeda, Takuya Diagn Microbiol Infect Dis Article Several automated high-throughput immunoassays for detecting anti-SARS-CoV-2 antibodies by a semi-quantitative approach have been commercialized. In this study, we describe the timeline of the antibody response in patients with RT-PCR-confirmed COVID-19. A total of 292 sequential serum samples from 33 Japanese patients were retrospectively analyzed using four test kits for SARS-CoV-2: the Abbott SARS-CoV-2 IgG assay (Abbott), Elecsys® Anti-SARS-CoV-2 assay (Roche Diagnostic), and VITROS® Anti-SARS-CoV-2 Total and IgG assays (Ortho Clinical Diagnostics). All automated immunoassays could equivalently identify positive sera collected within 2 weeks after symptom onset (99.3%–100%). In addition, the S protein-based automated immunoassay, the VITROS® Anti-SARS-CoV-2 Total assay, may play a complementary role in evaluating passive antibody therapies or vaccines against SARS-CoV-2, although further research is required. Elsevier Inc. 2021-07 2021-03-13 /pmc/articles/PMC7954771/ /pubmed/33744623 http://dx.doi.org/10.1016/j.diagmicrobio.2021.115370 Text en © 2021 Elsevier Inc. All rights reserved. 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 Kubota, Katsumi Kitagawa, Yutaro Matsuoka, Masaru Imai, Kazuo Orihara, Yuta Kawamura, Rieko Sakai, Jun Ishibashi, Noriomi Tarumoto, Norihito Takeuchi, Shinichi Maesaki, Shigefumi Maeda, Takuya Clinical evaluation of the antibody response in patients with COVID-19 using automated high-throughput immunoassays |
title | Clinical evaluation of the antibody response in patients with COVID-19 using automated high-throughput immunoassays |
title_full | Clinical evaluation of the antibody response in patients with COVID-19 using automated high-throughput immunoassays |
title_fullStr | Clinical evaluation of the antibody response in patients with COVID-19 using automated high-throughput immunoassays |
title_full_unstemmed | Clinical evaluation of the antibody response in patients with COVID-19 using automated high-throughput immunoassays |
title_short | Clinical evaluation of the antibody response in patients with COVID-19 using automated high-throughput immunoassays |
title_sort | clinical evaluation of the antibody response in patients with covid-19 using automated high-throughput immunoassays |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7954771/ https://www.ncbi.nlm.nih.gov/pubmed/33744623 http://dx.doi.org/10.1016/j.diagmicrobio.2021.115370 |
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