| Literature DB >> 33664294 |
Kenta Noda1, Kouki Matsuda2, Shigehiro Yagishita3, Kenji Maeda4, Yutaro Akiyama5, Junko Terada-Hirashima6,7, Hiromichi Matsushita8, Satoshi Iwata9, Kazuto Yamashita1, Yusuke Atarashi1, Shunsuke Watanabe1, Nobuyuki Ide10, Tomokazu Yoshida11, Norio Ohmagari5, Hiroaki Mitsuya2,12,13, Akinobu Hamada14.
Abstract
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.Entities:
Year: 2021 PMID: 33664294 DOI: 10.1038/s41598-021-84387-3
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379