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10.1177/00045632211015711

http://scihub22266oqcxt.onion/10.1177/00045632211015711
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33892600!ä!33892600

suck abstract from ncbi


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pmid33892600      Ann+Clin+Biochem 2021 ; 58 (5): 487-495
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  • Comparison of four high-throughput, automated immunoassays for the detection of SARS-CoV-2 antibodies #MMPMID33892600
  • Oakey J; Haslam S; Brown A; Eglin J; Houghton B; Singleton D
  • Ann Clin Biochem 2021[Sep]; 58 (5): 487-495 PMID33892600show ga
  • BACKGROUND: A number of immunoassays have been developed to measure antibodies specific to SARS-CoV-2. More data is required on their comparability, particularly among those with milder infections and in the general practice population. The aim of this study was to compare four high-throughput automated anti-SARS-CoV-2 assays using samples collected from hospitalized patients and healthcare workers with confirmed SARS-CoV-2 infection. In addition, we collected general practice samples to compare antibody results and determine seroprevalence. METHODS: Samples were collected from 57 hospitalized patients and nine healthcare workers at 14 days and at 28 days following confirmed SARS-CoV-2 infection. Samples were also collected from 225 patients presenting to general practice. Four assays were used: Abbott Architect IgG, Beckman Coulter DxI 800 IgG, Roche Cobas e801 total antibody and Siemens Advia Centaur XPT total antibody. RESULTS: All four assays showed concordance at 14 days in 83.9% of hospitalized patients and in 66.7% of healthcare workers. All four assays showed concordance at 28 days in 88.4% of hospitalized patients and 77.8% of healthcare workers. The sensitivity to detect recent infection was higher for the IgG assays than the total assays. All four assays showed concordance of 95.1% in the general practice population. Seroprevalence ranged from 4.9 to 5.8% depending on the assay used. CONCLUSIONS: All four assays showed excellent comparability, but it may be possible to obtain a negative result for any of the anti-SARS-CoV-2 assays in patients with confirmed previous SARS-CoV-2 infection. An equivocal range would be useful for all anti-SARS-CoV-2 assays.
  • |Adult[MESH]
  • |Aged[MESH]
  • |Aged, 80 and over[MESH]
  • |Antibodies, Viral/blood[MESH]
  • |COVID-19 Serological Testing/*methods/statistics & numerical data[MESH]
  • |COVID-19/*diagnosis/epidemiology/*immunology[MESH]
  • |Female[MESH]
  • |General Practice[MESH]
  • |Health Personnel[MESH]
  • |High-Throughput Screening Assays/methods/statistics & numerical data[MESH]
  • |Hospitalization[MESH]
  • |Humans[MESH]
  • |Immunoassay/methods/statistics & numerical data[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Pandemics[MESH]
  • |SARS-CoV-2/*immunology[MESH]
  • |Seroepidemiologic Studies[MESH]
  • |United Kingdom/epidemiology[MESH]


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