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Abstract
Virus neutralization remains the gold standard for determining antibody efficacy. Therefore, a high-throughput assay to measure SARS-CoV-2 neutralizing antibodies is urgently needed for COVID-19 serodiagnosis, convalescent plasma therapy, and vaccine development. Here, we report on a fluorescence-based SARS-CoV-2 neutralization assay that detects SARS-CoV-2 neutralizing antibodies in COVID-19 patient specimens and yields comparable results to plaque reduction neutralizing assay, the gold standard of serological testing. The fluorescence-based neutralization assay is specific to measure COVID-19 neutralizing antibodies without cross reacting with patient specimens with other viral, bacterial, or parasitic infections. Collectively, our approach offers a rapid platform that can be scaled to screen people for antibody protection from COVID-19, a key parameter necessary to safely reopen local communities.
Neutralizing antibody titers in SARS-CoV-2 infected or vaccinated people are an important measure for vaccine development and public health decision-making. Here, the authors develop a fluorescence based SARS-CoV-2 assay to determine neutralizing antibody titers in COVID-19 patient sera in a high throughput set-up.
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1 University of Texas Medical Branch, Department of Biochemistry and Molecular Biology, Galveston, USA (GRID:grid.176731.5) (ISNI:0000 0001 1547 9964); University of Texas Medical Branch, Department of Microbiology and Immunology, Galveston, USA (GRID:grid.176731.5) (ISNI:0000 0001 1547 9964)
2 University of Texas Medical Branch, Department of Biochemistry and Molecular Biology, Galveston, USA (GRID:grid.176731.5) (ISNI:0000 0001 1547 9964)
3 University of Texas Medical Branch, Department of Pathology, Galveston, USA (GRID:grid.176731.5) (ISNI:0000 0001 1547 9964)
4 University of Texas Medical Branch, Department of Biochemistry and Molecular Biology, Galveston, USA (GRID:grid.176731.5) (ISNI:0000 0001 1547 9964); Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore (GRID:grid.428397.3) (ISNI:0000 0004 0385 0924); University of Texas Medical Branch, Department of Internal Medicine, Galveston, USA (GRID:grid.176731.5) (ISNI:0000 0001 1547 9964)
5 University of Texas Medical Branch, Department of Microbiology and Immunology, Galveston, USA (GRID:grid.176731.5) (ISNI:0000 0001 1547 9964); University of Texas Medical Branch, Department of Pathology, Galveston, USA (GRID:grid.176731.5) (ISNI:0000 0001 1547 9964); University of Texas Medical Branch, Institute for Human Infections and Immunity, Galveston, USA (GRID:grid.176731.5) (ISNI:0000 0001 1547 9964)
6 University of Texas Medical Branch, Department of Biochemistry and Molecular Biology, Galveston, USA (GRID:grid.176731.5) (ISNI:0000 0001 1547 9964); University of Texas Medical Branch, Institute for Human Infections and Immunity, Galveston, USA (GRID:grid.176731.5) (ISNI:0000 0001 1547 9964); University of Texas Medical Branch, Sealy Institute for Vaccine Sciences, Galveston, USA (GRID:grid.176731.5) (ISNI:0000 0001 1547 9964); University of Texas Medical Branch, Sealy Center for Structural Biology & Molecular Biophysics, Galveston, USA (GRID:grid.176731.5) (ISNI:0000 0001 1547 9964); University of Texas Medical Branch, Institute for Translational Science, Galveston, USA (GRID:grid.176731.5) (ISNI:0000 0001 1547 9964)