A high-throughput neutralizing antibody assay for COVID-19 diagnosis and vaccine evaluation
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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.
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Together with reports of preserved neutralization of SARS-CoV-2 with key B.1.1.7 and B.1.351 spike mutations and of pseudovirus with the full B.1.1.7 spike mutation set, our data indicate broad BNT162b2-elicited immune recognition.
“Together with recent reports of the preserved neutralization of SARS-CoV-2 with key S mutations found in the B.1.1.7 and the B.1.351lineage 39,40 , and neutralization of pseudovirus bearing the full set of mutations of B.1.1.7 S 41 , our data indicate broad BNT162b2-elicited immune recognition 2,13,14 .”
From BNT162b2 vaccine induces neutralizing antibodies and poly-specific T cells in humans (2021) · cites this paper as [41]
The Results describe neutralization testing with COVID-19 patient sera, and the Discussion describes the assay’s use in vaccine trials. Our copy does not report BNT162b2-elicited immune recognition; searches for BNT162b2 and the B.1.1.7 and B.1.351 mutations found no supporting passage. The variant-neutralization reports in the citing sentence are attached to other citations. (LLM, conf=0.76)
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Self-citation
- Authors
- Muruato, A. E., Fontes-Garfias, C. R., Ren, P., Garcia-Blanco, M. A., Menachery, V. D., Xie, X., & Shi, P.-Y.
- Affiliations
- The University of Texas Medical Branch at Galveston (US)
- Corresponding author
- Xie, Xuping
- Shi, Pei-Yong
- ORCID
- Venue
- Nature Communications
- Published
- 2020-08-13
- Volume
- 11
- Issue
- 1
- Pages
- 4059-4059
- ISSN
- 2041-1723 (ISSN-L)
- PMC
- PMC7426916
- OpenAlex
- W3048799641
- Cited by
- 319
- References
- 18
- Citations by year
- 2026: 10 · 2025: 26 · 2024: 30 · 2023: 37 · 2022: 71 · 2021: 108 · 2020: 37
- FWCI
- 8.29
- Type
- journal article
- Language
- en
- Update notices
- correction (2021-06-22)
- Open access
- gold
- doi.org
- Locations
- Nature Communications (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- PubMed Central (submittedVersion, cc-by-nc-nd)
- RePEc: Research Papers in Economics (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- John S. Dunn Foundation
- Amon G. Carter Foundation
- Topics
- Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 and COVID-19 Research
- Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 detection and testing
- Health Sciences › Medicine › Infectious Diseases › COVID-19 Clinical Research Studies
- Keywords
- SARS-CoV-2, COVID-19 pandemic, neutralizing antibodies, virus neutralization assay, fluorometric assay, COVID-19 diagnosis, vaccine evaluation, convalescent plasma therapy, antibody cross-reactivity
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