Rapid and accurate agglutination-based testing for SARS-CoV-2 antibodies

Cell Rep Methods. 2021 Jun 21;1(2):100011. doi: 10.1016/j.crmeth.2021.100011. Epub 2021 May 12.

Abstract

We have developed a rapid, accurate, and cost-effective serologic test for SARS-CoV-2 virus, which caused the COVID-19 pandemic, on the basis of antibody-dependent agglutination of antigen-coated latex particles. When validated using plasma samples that are positive or negative for SARS-CoV-2, the agglutination assay detected antibodies against the receptor-binding domain of the spike (S-RBD) or the nucleocapsid protein of SARS-CoV-2 with 100% specificity and ∼98% sensitivity. Furthermore, we found that the strength of the S-RBD antibody response measured by the agglutination assay correlated with the efficiency of the plasma in blocking RBD binding to the angiotensin-converting enzyme 2 in a surrogate neutralization assay, suggesting that the agglutination assay might be used to identify individuals with virus-neutralizing antibodies. Intriguingly, we found that >92% of patients had detectable antibodies on the day of a positive viral RNA test, suggesting that the agglutination antibody test might complement RNA testing for the diagnosis of SARS-CoV-2 infection.

Keywords: COVID-19; SARS-CoV-2; agglutination assay; antibody test; neutralizing antibody; nucleocapsid; rapid testing; serology; spike.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Agglutination
  • Antibodies, Viral
  • COVID-19* / diagnosis
  • Humans
  • Pandemics
  • SARS-CoV-2*

Substances

  • Antibodies, Viral