Abstract
More than 24 million infections with the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) were confirmed globally by September 2020. While polymerase chain reaction-based assays are used for diagnosis, there is a need for high-throughput, rapid serologic methods. A Luminex binding assay was developed and used to assess simultaneously the presence of coronavirus disease 2019 (COVID-19)-specific antibodies in human serum and plasma. Clear differentiation was achieved between specimens from infected and uninfected subjects, and a wide range of serum/plasma antibody levels was delineated in infected subjects. All 25 specimens from 18 patients with COVID-19 were positive in the assays with both the trimeric spike and the receptor-binding domain proteins. None of the 13 specimens from uninfected subjects displayed antibodies to either antigen. There was a highly statistically significant difference between the antibody levels of COVID-19-infected and -uninfected specimens (P
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Weiss, S., Klingler, J., Hioe, C., Amanat, F., Baine, I., Arinsburg, S., … Zolla-Pazner, S. (2020). A high-throughput assay for circulating antibodies directed against the s protein of severe acute respiratory syndrome coronavirus 2. Journal of Infectious Diseases, 222(10), 1629–1634. https://doi.org/10.1093/infdis/jiaa531
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