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Multiplexed, quantitative serological profiling of COVID-19 from a drop of blood by a point-of-care test

Highly sensitive, specific, and point-of-care (POC) serological assays are an essential tool to manage the COVID-19 pandemic. Here, we report on a microfluidic, multiplexed POC test that can profile the antibody response against multiple SARS-CoV-2 antigens—Spike S1 (S1), Nucleocapsid (N), and the r...

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Detalles Bibliográficos
Autores principales: Heggestad, Jacob T., Kinnamon, David S., Olson, Lyra B., Liu, Jason, Kelly, Garrett, Wall, Simone A., Fontes, Cassio M., Joh, Daniel Y., Hucknall, Angus M., Pieper, Carl, Naqvi, Ibtehaj A., Chen, Lingye, Que, Loretta G., Oguin, Thomas, Nair, Smita K., Sullenger, Bruce A., Woods, Christopher W., Sempowski, Gregory D., Kraft, Bryan D., Chilkoti, Ashutosh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7654894/
https://www.ncbi.nlm.nih.gov/pubmed/33173900
http://dx.doi.org/10.1101/2020.11.05.20226654
Descripción
Sumario:Highly sensitive, specific, and point-of-care (POC) serological assays are an essential tool to manage the COVID-19 pandemic. Here, we report on a microfluidic, multiplexed POC test that can profile the antibody response against multiple SARS-CoV-2 antigens—Spike S1 (S1), Nucleocapsid (N), and the receptor binding domain (RBD)—simultaneously from a 60 μL drop of blood, plasma, or serum. We assessed the levels of anti-SARS-CoV-2 antibodies in plasma samples from 19 individuals (at multiple time points) with COVID-19 that required admission to the intensive care unit and from 10 healthy individuals. This POC assay shows good concordance with a live virus microneutralization assay, achieved high sensitivity (100%) and specificity (100%), and successfully tracked the longitudinal evolution of the antibody response in infected individuals. We also demonstrated that we can detect a chemokine, IP-10, on the same chip, which may provide prognostic insight into patient outcomes. Because our test requires minimal user intervention and is read by a handheld detector, it can be globally deployed in the fight against COVID-19 by democratizing access to laboratory quality tests.