AI Article Synopsis

  • * This test showed 100% specificity and about 98% sensitivity when validating it with blood plasma samples, effectively identifying antibodies related to the virus.
  • * Our findings indicate that over 92% of patients had detectable antibodies on the same day they tested positive for the virus, suggesting this test could enhance diagnosis when used alongside traditional RNA testing.

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8114573PMC
http://dx.doi.org/10.1016/j.crmeth.2021.100011DOI Listing

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