Abstract

Diagnostic tests that detect antibodies (AB) against SARS-CoV-2 for evaluation of seroprevalence and guidance of health care measures are important tools for managing the COVID-19 pandemic. Current tests have certain limitations with regard to turnaround time, costs and availability, particularly in point-of-care (POC) settings. We established a hemagglutination-based AB test that is based on bi-specific proteins which contain a dromedary-derived antibody (nanobody) binding red blood cells (RBD) and a SARS-CoV-2-derived antigen, such as the receptor-binding domain of the Spike protein (Spike-RBD). While the nanobody mediates swift binding to RBC, the antigen moiety directs instantaneous, visually apparent hemagglutination in the presence of SARS-CoV-2-specific AB generated in COVID-19 patients or vaccinated individuals. Method comparison studies with assays cleared by emergency use authorization demonstrate high specificity and sensitivity. To further increase objectivity of test interpretation, we developed an image analysis tool based on digital image acquisition (via a cell phone) and a machine learning algorithm based on defined sample-training and -validation datasets. Preliminary data, including a small clinical study, provides proof of principle for test performance in a POC setting. Together, the data support the interpretation that this AB test format, which we refer to as ‘NanoSpot.ai’, is suitable for POC testing, can be manufactured at very low costs and, based on its generic mode of action, can likely be adapted to a variety of other pathogens.

Details

Title
A rapid and affordable point of care test for antibodies against SARS-CoV-2 based on hemagglutination and artificial intelligence interpretation
Author
Redecke Vanessa 1 ; Tawaratsumida Kazuki 1 ; Larragoite, Erin T 2 ; Williams Elizabeth S C P 2 ; Planelles Vicente 2 ; Spivak, Adam M 3 ; Hirayama Lincoln 4 ; Elgort, Marc 4 ; Swenson, Shane 5 ; Smith, Rick 5 ; Worthen, Bryan 5 ; Zimmerman, Russ 5 ; Slev, Patricia 4 ; Cahoon, Ben 5 ; Astill, Mark 4 ; Häcker, Hans 1 

 University of Utah School of Medicine, Laboratory of Innate Immunity and Signal Transduction, Division of Microbiology and Immunology, Department of Pathology, Salt Lake City, USA (GRID:grid.223827.e) (ISNI:0000 0001 2193 0096) 
 University of Utah School of Medicine, Division of Microbiology and Immunology, Department of Pathology, Salt Lake City, USA (GRID:grid.223827.e) (ISNI:0000 0001 2193 0096) 
 University of Utah School of Medicine, Division of Infectious Diseases, Department of Medicine, Salt Lake City, USA (GRID:grid.223827.e) (ISNI:0000 0001 2193 0096) 
 Associated Regional and University Pathologists (ARUP) Laboratories, Salt Lake City, USA (GRID:grid.223827.e) (ISNI:0000 0001 2193 0096) 
 Techcyte Inc., Lindon, USA (GRID:grid.223827.e) 
Publication year
2021
Publication date
2021
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2615376254
Copyright
© The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.