Author:
Kainulainen Markus H.,Bergeron Eric,Chatterjee Payel,Chapman Asheley P.,Lee Joo,Chida Asiya,Tang Xiaoling,Wharton Rebekah E.,Mercer Kristina B.,Petway Marla,Jenks Harley M.,Flietstra Timothy D.,Schuh Amy J.,Satheshkumar Panayampalli S.,Chaitram Jasmine M.,Owen S. Michele,McMullan Laura K.,Flint Mike,Finn M. G.,Goldstein Jason M.,Montgomery Joel M.,Spiropoulou Christina F.
Abstract
AbstractSARS-CoV-2 emerged in late 2019 and has since spread around the world, causing a pandemic of the respiratory disease COVID-19. Detecting antibodies against the virus is an essential tool for tracking infections and developing vaccines. Such tests, primarily utilizing the enzyme-linked immunosorbent assay (ELISA) principle, can be either qualitative (reporting positive/negative results) or quantitative (reporting a value representing the quantity of specific antibodies). Quantitation is vital for determining stability or decline of antibody titers in convalescence, efficacy of different vaccination regimens, and detection of asymptomatic infections. Quantitation typically requires two-step ELISA testing, in which samples are first screened in a qualitative assay and positive samples are subsequently analyzed as a dilution series. To overcome the throughput limitations of this approach, we developed a simpler and faster system that is highly automatable and achieves quantitation in a single-dilution screening format with sensitivity and specificity comparable to those of ELISA.
Funder
Centers for Disease Control and Prevention
Publisher
Springer Science and Business Media LLC
Cited by
14 articles.
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