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A hemagglutination-based, semi-quantitative test for point-of-care determination of SARS-CoV-2 antibody levels
Robert Kruse; Yuting Huang; Alyssa Lee; Xianming Zhu; Ruchee Shrestha; Oliver Laeyendecker; Kirsten Littlefield; Andy Pekosz; Evan M Bloch; Aaron A.R. Tobian; Zack Z Wang.
Affiliation
  • Robert Kruse; Department of Pathology, Johns Hopkins University School of Medicine
  • Yuting Huang; Department of Medicine, University of Maryland Medical Center Midtown Campus
  • Alyssa Lee; Johns Hopkins University School of Medicine
  • Xianming Zhu; Department of Pathology, Johns Hopkins University School of Medicine
  • Ruchee Shrestha; Department of Medicine, Johns Hopkins University School of Medicine
  • Oliver Laeyendecker; Department of Medicine, Johns Hopkins University School of Medicine
  • Kirsten Littlefield; Department of Molecular Microbiology and Immunology, The Johns Hopkins Bloomberg School of Public Health
  • Andy Pekosz; Department of Molecular Microbiology and Immunology, The Johns Hopkins Bloomberg School of Public Health
  • Evan M Bloch; Department of Pathology, Johns Hopkins University School of Medicine
  • Aaron A.R. Tobian; Department of Pathology, Johns Hopkins University School of Medicine
  • Zack Z Wang; Department of Medicine, Johns Hopkins University School of Medicine
Preprint in English | medRxiv | ID: ppmedrxiv-21256452
Journal article
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ABSTRACT
Serologic, point-of-care tests to detect antibodies against SARS-CoV-2 are an important tool in the COVID-19 pandemic. The majority of current point-of-care antibody tests developed for SARS-CoV-2 rely on lateral flow assays, but these do not offer quantitative information. To address this, we developed a new method of COVID-19 antibody testing employing hemagglutination tested on a dry card, similar to that which is already available for rapid typing of ABO blood groups. A fusion protein linking red blood cells (RBCs) to the receptor-binding domain (RBD) of SARS-CoV-2 spike protein was placed on the card. 200 COVID-19 patient and 200 control plasma samples were reconstituted with O-negative RBCs to form whole blood and added to the dried protein, followed by a stirring step and a tilting step, 3-minute incubation, and a second tilting step. The sensitivity for the hemagglutination test, Euroimmun IgG ELISA test and RBD-based CoronaChek lateral flow assay was 87.0%, 86.5%, and 84.5%, respectively, using samples obtained from recovered COVID-19 individuals. Testing pre-pandemic samples, the hemagglutination test had a specificity of 95.5%, compared to 97.3% and 98.9% for the ELISA and CoronaChek, respectively. A distribution of agglutination strengths was observed in COVID-19 convalescent plasma samples, with the highest agglutination score (4) exhibiting significantly higher neutralizing antibody titers than weak positives (2) (p<0.0001). Strong agglutinations were observed within 1 minute of testing, and this shorter assay time also increased specificity to 98.5%. In conclusion, we developed a novel rapid, point-of-care RBC agglutination test for the detection of SARS-CoV-2 antibodies that can yield semi-quantitative information on neutralizing antibody titer in patients. The five-minute test may find use in determination of serostatus prior to vaccination, post-vaccination surveillance and travel screening.
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Full text: Available Collection: Preprints Database: medRxiv Type of study: Diagnostic study / Experimental_studies / Prognostic study / Rct Language: English Year: 2021 Document type: Preprint
Full text: Available Collection: Preprints Database: medRxiv Type of study: Diagnostic study / Experimental_studies / Prognostic study / Rct Language: English Year: 2021 Document type: Preprint
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