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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...

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Detalles Bibliográficos
Autores principales: Kubota, Katsumi, Kitagawa, Yutaro, Matsuoka, Masaru, Imai, Kazuo, Orihara, Yuta, Kawamura, Rieko, Sakai, Jun, Ishibashi, Noriomi, Tarumoto, Norihito, Takeuchi, Shinichi, Maesaki, Shigefumi, Maeda, Takuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2021
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
Descripción
Sumario: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.