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10.3390/diagnostics10080593

http://scihub22266oqcxt.onion/10.3390/diagnostics10080593
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suck abstract from ncbi


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pmid32823852      Diagnostics+(Basel) 2020 ; 10 (8): ä
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  • EDTA-Anticoagulated Whole Blood for SARS-CoV-2 Antibody Testing by Electrochemiluminescence Immunoassay (ECLIA) and Enzyme-Linked Immunosorbent Assay (ELISA) #MMPMID32823852
  • Kovac M; Risch L; Thiel S; Weber M; Grossmann K; Wohlwend N; Lung T; Hillmann D; Ritzler M; Bigler S; Ferrara F; Bodmer T; Egli K; Imperiali M; Heer S; Salimi Y; Renz H; Kohler P; Vernazza P; Kahlert CR; Paprotny M; Risch M
  • Diagnostics (Basel) 2020[Aug]; 10 (8): ä PMID32823852show ga
  • While lateral flow test formats can be utilized with whole blood and low sample volumes, their diagnostic characteristics are inferior to immunoassays based on chemiluminescence immunoassay (CLIA) or enzyme-linked immunosorbent assay (ELISA) technology. CLIAs and ELISAs can be automated to a high degree but commonly require larger serum or plasma volumes for sample processing. We addressed the suitability of EDTA-anticoagulated whole blood as an alternative sample material for antibody testing against SARS-CoV-2 by electro-CLIA (ECLIA; Roche, Rotkreuz, Switzerland) and ELISA (IgG and IgA; Euroimmun, Germany). Simultaneously drawn venous serum and EDTA-anticoagulated whole blood samples from 223 individuals were included. Correction of the whole blood results for hematocrit led to a good agreement with the serum results for weakly to moderately positive antibody signals. In receiver-operating characteristic curve analysis, all three assays displayed comparable diagnostic accuracy (area under the curve (AUC)) using corrected whole blood and serum (AUCs: 0.97 for ECLIA and IgG ELISA; 0.84 for IgA ELISA). In conclusion, our results suggest that the investigated assays can reliably detect antibodies against SARS-CoV-2 in hemolyzed whole blood anticoagulated with EDTA. Correction of these results for hematocrit is suggested. This study demonstrates that the automated processing of whole blood for identification of SARS-CoV-2 antibodies with common ECLIA and ELISA methods is accurate and feasible.
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