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Comparative analysis of antigen-specific anti-SARS-CoV-2 antibody isotypes in COVID-19 patients
Hidetsugu Fujigaki; Masato Inaba; Michiko Osawa; Saya Moriyama; Yoshimasa Takahashi; Tadaki Suzuki; Kenya Yamase; Yukihiro Yoshida; Yo Yagura; Takayoshi Oyamada; Masao Takemura; Yohei Doi; Kuniaki Saito.
Affiliation
  • Hidetsugu Fujigaki; Fujita Health University Graduate School of Health Sciences
  • Masato Inaba; Fujita Health University School of Medicine
  • Michiko Osawa; Fujita Health University Hospital
  • Saya Moriyama; National Institute of Infectious Diseases
  • Yoshimasa Takahashi; National Institute of Infectious Diseases
  • Tadaki Suzuki; National Institute of Infectious Diseases
  • Kenya Yamase; FUJIFILM Wako Pure Chemical Corporation
  • Yukihiro Yoshida; FUJIFILM Wako Pure Chemical Corporation
  • Yo Yagura; FUJIFILM Wako Pure Chemical Corporation
  • Takayoshi Oyamada; FUJIFILM Corporation
  • Masao Takemura; Fujita Health University Graduate School of Health Sciences
  • Yohei Doi; Fujita Health University School of Medicine
  • Kuniaki Saito; Fujita Health University Graduate School of Health Sciences
Preprint in English | bioRxiv | ID: ppbiorxiv-407510
Journal article
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ABSTRACT
Serological tests for detection of anti-severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antibodies in blood are expected to identify individuals who have acquired immunity against SARS-CoV-2 and indication of seroprevalence of SARS-CoV-2 infection. Many serological tests have been developed to detect antibodies against SARS-CoV-2. However, these tests have considerable variations in their specificity and sensitivity, and whether they can predict levels of neutralizing activity is yet to be determined. This study aimed to investigate the kinetics and neutralizing activity of various antigen-specific antibody isotypes against SARS-CoV-2 in serum of coronavirus disease 2019 (COVID-19) patients confirmed via polymerase chain reaction test. We developed IgG, IgM and IgA measurement assays for each antigen, including receptor-binding domain (RBD) of spike (S) protein, S1 domain, full length S protein, S trimer and nucleocapsid (N) domain, based on enzyme-linked immunosorbent assay. The assays of the S protein for all isotypes showed high specificity, while the assays for all isotypes against N protein showed lower specificity. The sensitivity of all antigen-specific antibody isotypes depended on the timing of the serum collection and all of them, except for IgM against N protein, reached more than 90% at 15-21 days post-symptom onset. The best correlation with virus neutralizing activity was found for IgG against RBD (RBD-IgG), and levels of RBD-IgG in sera from four severe COVID-19 patients increased concordantly with neutralizing activity. Our results provide valuable information regarding the selection of serological test for seroprevalence and vaccine evaluation studies.
License
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Full text: Available Collection: Preprints Database: bioRxiv Type of study: Diagnostic study / Experimental_studies / Observational study / Prognostic study Language: English Year: 2020 Document type: Preprint
Full text: Available Collection: Preprints Database: bioRxiv Type of study: Diagnostic study / Experimental_studies / Observational study / Prognostic study Language: English Year: 2020 Document type: Preprint
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