A novel highly quantitative and reproducible assay for the detection of anti-SARS-CoV-2 IgG and IgM antibodies

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作者
Kenta Noda
Kouki Matsuda
Shigehiro Yagishita
Kenji Maeda
Yutaro Akiyama
Junko Terada-Hirashima
Hiromichi Matsushita
Satoshi Iwata
Kazuto Yamashita
Yusuke Atarashi
Shunsuke Watanabe
Nobuyuki Ide
Tomokazu Yoshida
Norio Ohmagari
Hiroaki Mitsuya
Akinobu Hamada
机构
[1] Sysmex Corporation,Central Research Laboratories
[2] National Center for Global Health and Medicine (NCGM) Research Institute,Department of Refractory Viral Infections
[3] National Cancer Center Research Institute,Division of Molecular Pharmacology
[4] NCGM,Disease Control and Prevention Center (DCC)
[5] NCGM,Center for Clinical Science
[6] NCGM Center Hospital,Respiratory Medicine
[7] National Cancer Center Hospital,Department of Laboratory Medicine
[8] National Cancer Center Hospital,Department of Infectious Diseases
[9] Sysmex Corporation,Bio
[10] National Cancer Institute,Diagnostic Reagent Technology Center
[11] National Institutes of Health,Experimental Retrovirology Section, HIV and AIDS Malignancy Branch
[12] Kumamoto University Hospital,Department of Clinical Sciences
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The quantitative range and reproducibility of current serological tests for severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) are not optimized. Herein, we developed a diagnostic test that detects SARS-CoV-2 IgG and IgM with high quantitativeness and reproducibility and low interference. The system was based on the high-sensitivity chemiluminescence enzyme immunoassay (HISCL) platform and detects IgG and IgM specific to SARS-CoV-2 spike and nucleocapsid proteins. Quantification accuracy and reproducibility were evaluated using serially diluted samples from 60 SARS-CoV-2-infected patients. Assay performance was evaluated using serum samples from the SARS-CoV-2-infected patients and 500 SARS-CoV-2-negative serum samples collected before the emergence of SARS-CoV-2. The system showed high quantification accuracy (range, 102), high reproducibility (within 5%), and no cross-reaction between SARS1- and MERS-S proteins. Detection accuracy was 98.3% and 93.3% for IgG and IgM against spike proteins and 100% and 71.7% for IgG and IgM against nucleocapsid proteins, respectively. Mean antibody levels were > 10 times that in negative samples upon admission and > 100 times that at convalescent periods. Clinical severity upon admission was not correlated with IgG or IgM levels. This highly quantitative, reproducible assay system with high clinical performance may help analyze temporal serological/immunological profiles of SARS-CoV-2 infection and SARS-CoV-2 vaccine effectiveness.
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