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. 2021 Apr;70(4):001291.
doi: 10.1099/jmm.0.001291.

Clinical characteristics and antibody response to SARS-CoV-2 spike 1 protein using VITROS Anti-SARS-CoV-2 antibody tests in COVID-19 patients in Japan

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Clinical characteristics and antibody response to SARS-CoV-2 spike 1 protein using VITROS Anti-SARS-CoV-2 antibody tests in COVID-19 patients in Japan

Mayu Nagura-Ikeda et al. J Med Microbiol. 2021 Apr.

Abstract

Introduction. Serological tests for COVID-19 are important in providing results for surveillance and supporting diagnosis. Investigating the serological response in COVID-19 patients with different disease severity is important for assessing the clinical utility of serological assays.Gap Statement. However, few studies have investigated the clinical utility of antibody assays for COVID-19 or differences in antibody response in association with disease severity.Aim. The study aimed to evaluate the clinical characteristics and clinical utility of VITROS SARS-CoV-2 antibody tests according to COVID-19 severity in patients in Japan.Methodology. We analysed 255 serum specimens from 130 COVID-19 patients and examined clinical records and laboratory data. Presence of total (IgA, IgM, and IgG) and specific IgG antibody for the spike 1 antigen of SARS-CoV-2 was determined using VITROS Anti-SARS-CoV-2 antibody tests.Results. Overall, 98 (75.4 %) and 32 (24.6 %) patients had mild and severe COVID-19, respectively. On admission, 76 (58.5 %) and 45 (34.6 %) patients were positive for total and IgG antibody assays. Among 91 patients at discharge, 90 (98.9 %) and 81 (89.0 %) were positive for total and IgG antibody, respectively. Clinical background and laboratory findings on admission, but not the prevalence or concentration of total or IgG antibody, were associated with disease prognosis. Total and IgG antibody intensities were significantly higher in severe cases than in mild cases in serum collected >11 days after onset, but not within 10 days.Conclusion. VITROS Anti-SARS-CoV-2 total and IgG assays will be useful as supporting diagnostic and surveillance tools and for evaluation of humoral immune response to COVID-19. Optimal prediction of disease prognosis is made from considering both clinical history and laboratory findings.

Keywords: COVID-19; Japan; SARS-CoV-2; antibody; chemiluminescent immunoassay.

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Conflict of interest statement

The authors declare that there are no conflicts of interest.

Figures

Fig. 1.
Fig. 1.
Seropositive rate of total and IgG antibody response in serum specimens collected from mild and severe COVID-19 cases after symptom onset. Plot shows seropositive rate for total and IgG antibody assays per total serum collected from symptom onset. Solid and dashed lines indicate total and IgG antibody assays, respectively. Blue and red lines indicate mild and severe cases, respectively. Ab, antibody.
Fig. 2.
Fig. 2.
Kinetics of total and IgG antibody response between mild and severe cases. Plots show time to sample collection from symptom onset and signal for test sample/signal at cutoff [S/CO] for total and IgG antibodies. (a) Total antibody, (b) IgG antibody. Blue and red lines indicate regression curves of mild and severe cases, respectively. Ab, antibody.
Fig. 3.
Fig. 3.
Comparison between mild and severe cases of total and IgG antibody response for total antibody (a–c) and IgG antibody (d, e) in serum specimens collected at different timings from symptom onset. Correlation coefficient calculated using Wilcoxon’s rank-sum test. *P<0.05, **P<0.001. Ab, antibody.

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