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10.3343/alm.2021.41.6.577

http://scihub22266oqcxt.onion/10.3343/alm.2021.41.6.577
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suck abstract from ncbi


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pmid34108285      Ann+Lab+Med 2021 ; 41 (6): 577-587
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  • Comparison of SARS-CoV-2 Antibody Responses and Seroconversion in COVID-19 Patients Using Twelve Commercial Immunoassays #MMPMID34108285
  • Yun S; Ryu JH; Jang JH; Bae H; Yoo SH; Choi AR; Jo SJ; Lim J; Lee J; Ryu H; Cho SY; Lee DG; Lee J; Kim SC; Park YJ; Lee H; Oh EJ
  • Ann Lab Med 2021[Nov]; 41 (6): 577-587 PMID34108285show ga
  • BACKGROUND: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antibody assays have high clinical utility in managing the pandemic. We compared antibody responses and seroconversion of coronavirus disease 2019 (COVID-19) patients using different immunoassays. METHODS: We evaluated 12 commercial immunoassays, including three automated chemiluminescent immunoassays (Abbott, Roche, and Siemens), three enzyme immunoassays (Bio-Rad, Euroimmun, and Vircell), five lateral flow immunoassays (Boditech Med, SD biosensor, PCL, Sugentech, and Rapigen), and one surrogate neutralizing antibody assay (GenScript) in sequential samples from 49 COVID-19 patients and 10 seroconversion panels. RESULTS: The positive percent agreement (PPA) of assays for a COVID-19 diagnosis ranged from 84.0% to 98.5% for all samples (>14 days after symptom onset), with IgM or IgA assays showing higher PPAs. Seroconversion responses varied across the assay type and disease severity. Assays targeting the spike or receptor-binding domain protein showed a tendency for early seroconversion detection and higher index values in patients with severe disease. Index values from SARS-CoV-2 binding antibody assays (three automated assays, one LFIA, and three EIAs) showed moderate to strong correlations with the neutralizing antibody percentage (r=0.517-0.874), and stronger correlations in patients with severe disease and in assays targeting spike protein. Agreement among the 12 assays was good (74.3%-96.4%) for detecting IgG or total antibodies. CONCLUSIONS: Positivity rates and seroconversion of SARS-CoV-2 antibodies vary depending on the assay kits, disease severity, and antigen target. This study contributes to a better understanding of antibody response in symptomatic COVID-19 patients using currently available assays.
  • |Antibodies, Viral/*analysis[MESH]
  • |COVID-19 Testing/*methods[MESH]
  • |COVID-19/*diagnosis/pathology/virology[MESH]
  • |Humans[MESH]
  • |Immunoassay[MESH]
  • |Immunoglobulin A/analysis[MESH]
  • |Immunoglobulin G/analysis[MESH]
  • |Immunoglobulin M/analysis[MESH]
  • |Reagent Kits, Diagnostic[MESH]
  • |SARS-CoV-2/*immunology/isolation & purification[MESH]
  • |Sensitivity and Specificity[MESH]


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