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Multiplexed, quantitative serological profiling of COVID-19 from a drop of blood by a point-of-care test
Jacob T Heggestad; David Kinnamon; Lyra Olson; Jason Liu; Garrett Kelly; Simone Wall; Cassio Fontes; Daniel Joh; Angus Hucknall; Carl Pieper; Ibtehaj Naqvi; Lingye Chen; Loretta Que; Thomas Oguin III; Smita Nair; Bruce Sullenger; Christopher Woods; Gregory Sempowski; Bryan Kraft; Asutosh Chilkoti.
Affiliation
  • Jacob T Heggestad; Duke University
  • David Kinnamon; Duke University
  • Lyra Olson; Duke University
  • Jason Liu; Duke University
  • Garrett Kelly; Duke University
  • Simone Wall; Duke University
  • Cassio Fontes; Duke University
  • Daniel Joh; Duke University
  • Angus Hucknall; Duke University
  • Carl Pieper; Duke University
  • Ibtehaj Naqvi; Duke University
  • Lingye Chen; Duke University
  • Loretta Que; Duke University
  • Thomas Oguin III; Duke University
  • Smita Nair; Duke University
  • Bruce Sullenger; Duke University
  • Christopher Woods; Duke University School of Medicine
  • Gregory Sempowski; Duke University
  • Bryan Kraft; Duke University
  • Asutosh Chilkoti; Duke University
Preprint in English | medRxiv | ID: ppmedrxiv-20226654
ABSTRACT
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 {micro}L 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.
License
cc_by_nc_nd
Full text: Available Collection: Preprints Database: medRxiv Type of study: Diagnostic study / Prognostic study Language: English Year: 2020 Document type: Preprint
Full text: Available Collection: Preprints Database: medRxiv Type of study: Diagnostic study / Prognostic study Language: English Year: 2020 Document type: Preprint
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