Nature Medicine, volume 26, issue 9, pages 1422-1427
Rapid isolation and profiling of a diverse panel of human monoclonal antibodies targeting the SARS-CoV-2 spike protein
Seth J. Zost
1
,
Pavlo Gilchuk
1
,
Rita E. Chen
2, 3
,
James Brett Case
3
,
Joseph X Reidy
1
,
Andrew Trivette
1
,
Rachel S. Nargi
1
,
Rachel E. Sutton
1
,
Naveenchandra Suryadevara
1
,
Elaine C. Chen
4
,
Elad Binshtein
1
,
Swathi Shrihari
3
,
Mario Ostrowski
5
,
Helen Y. Chu
6
,
Jonathan E. Didier
7
,
Keith W MacRenaris
7
,
Taylor Jones
1
,
Samuel Day
1
,
Luke Myers
1
,
F. Eun-Hyung Lee
8
,
Doan C. Nguyen
8
,
Ignacio Sanz
8
,
David R. Martinez
9
,
Paul W Rothlauf
10, 11
,
Louis Marie Bloyet
11
,
Sean Whelan
10, 11
,
Ralph S Baric
9
,
Larissa B Thackray
3
,
Michael S. Diamond
2, 3, 11, 12
,
Robert H. Carnahan
1, 13
,
James Crowe
1, 4, 13
7
Berkeley Lights, Inc., Emeryville, USA
|
Publication type: Journal Article
Publication date: 2020-07-10
Journal:
Nature Medicine
Q1
Q1
SJR: 19.045
CiteScore: 100.9
Impact factor: 58.7
ISSN: 10788956, 1546170X, 17447933
PubMed ID:
32651581
General Biochemistry, Genetics and Molecular Biology
General Medicine
Abstract
Antibodies are a principal determinant of immunity for most RNA viruses and have promise to reduce infection or disease during major epidemics. The novel coronavirus SARS-CoV-2 has caused a global pandemic with millions of infections and hundreds of thousands of deaths to date1,2. In response, we used a rapid antibody discovery platform to isolate hundreds of human monoclonal antibodies (mAbs) against the SARS-CoV-2 spike (S) protein. We stratify these mAbs into five major classes on the basis of their reactivity to subdomains of S protein as well as their cross-reactivity to SARS-CoV. Many of these mAbs inhibit infection of authentic SARS-CoV-2 virus, with most neutralizing mAbs recognizing the receptor-binding domain (RBD) of S. This work defines sites of vulnerability on SARS-CoV-2 S and demonstrates the speed and robustness of advanced antibody discovery platforms. A platform for rapid antibody discovery enabled the isolation of hundreds of human monoclonal antibodies against SARS-CoV-2 and the prioritization of potent antibody candidates for clinical trials in patients with COVID-19.
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Zost S. J. et al. Rapid isolation and profiling of a diverse panel of human monoclonal antibodies targeting the SARS-CoV-2 spike protein // Nature Medicine. 2020. Vol. 26. No. 9. pp. 1422-1427.
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Zost S. J., Gilchuk P., Chen R. E., Case J. B., Reidy J. X., Trivette A., Nargi R. S., Sutton R. E., Suryadevara N., Chen E. C., Binshtein E., Shrihari S., Ostrowski M., Chu H. Y., Didier J. E., MacRenaris K. W., Jones T., Day S., Myers L., Lee F. E., Nguyen D. C., Sanz I., Martinez D. R., Rothlauf P. W., Bloyet L. M., Whelan S., Baric R. S., Thackray L. B., Diamond M., Carnahan R. H., Crowe J. Rapid isolation and profiling of a diverse panel of human monoclonal antibodies targeting the SARS-CoV-2 spike protein // Nature Medicine. 2020. Vol. 26. No. 9. pp. 1422-1427.
Cite this
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TY - JOUR
DO - 10.1038/s41591-020-0998-x
UR - https://doi.org/10.1038/s41591-020-0998-x
TI - Rapid isolation and profiling of a diverse panel of human monoclonal antibodies targeting the SARS-CoV-2 spike protein
T2 - Nature Medicine
AU - Zost, Seth J.
AU - Gilchuk, Pavlo
AU - Chen, Rita E.
AU - Case, James Brett
AU - Reidy, Joseph X
AU - Trivette, Andrew
AU - Nargi, Rachel S.
AU - Sutton, Rachel E.
AU - Suryadevara, Naveenchandra
AU - Chen, Elaine C.
AU - Binshtein, Elad
AU - Shrihari, Swathi
AU - Ostrowski, Mario
AU - Chu, Helen Y.
AU - Didier, Jonathan E.
AU - MacRenaris, Keith W
AU - Jones, Taylor
AU - Day, Samuel
AU - Myers, Luke
AU - Lee, F. Eun-Hyung
AU - Nguyen, Doan C.
AU - Sanz, Ignacio
AU - Martinez, David R.
AU - Rothlauf, Paul W
AU - Bloyet, Louis Marie
AU - Whelan, Sean
AU - Baric, Ralph S
AU - Thackray, Larissa B
AU - Diamond, Michael S.
AU - Carnahan, Robert H.
AU - Crowe, James
PY - 2020
DA - 2020/07/10
PB - Springer Nature
SP - 1422-1427
IS - 9
VL - 26
PMID - 32651581
SN - 1078-8956
SN - 1546-170X
SN - 1744-7933
ER -
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@article{2020_Zost,
author = {Seth J. Zost and Pavlo Gilchuk and Rita E. Chen and James Brett Case and Joseph X Reidy and Andrew Trivette and Rachel S. Nargi and Rachel E. Sutton and Naveenchandra Suryadevara and Elaine C. Chen and Elad Binshtein and Swathi Shrihari and Mario Ostrowski and Helen Y. Chu and Jonathan E. Didier and Keith W MacRenaris and Taylor Jones and Samuel Day and Luke Myers and F. Eun-Hyung Lee and Doan C. Nguyen and Ignacio Sanz and David R. Martinez and Paul W Rothlauf and Louis Marie Bloyet and Sean Whelan and Ralph S Baric and Larissa B Thackray and Michael S. Diamond and Robert H. Carnahan and James Crowe},
title = {Rapid isolation and profiling of a diverse panel of human monoclonal antibodies targeting the SARS-CoV-2 spike protein},
journal = {Nature Medicine},
year = {2020},
volume = {26},
publisher = {Springer Nature},
month = {jul},
url = {https://doi.org/10.1038/s41591-020-0998-x},
number = {9},
pages = {1422--1427},
doi = {10.1038/s41591-020-0998-x}
}
Cite this
MLA
Copy
Zost, Seth J., et al. “Rapid isolation and profiling of a diverse panel of human monoclonal antibodies targeting the SARS-CoV-2 spike protein.” Nature Medicine, vol. 26, no. 9, Jul. 2020, pp. 1422-1427. https://doi.org/10.1038/s41591-020-0998-x.