LY-CoV1404 (bebtelovimab) potently neutralizes SARS-CoV-2 variants

Kathryn Westendorf(AbCellera (Canada)), Stefanie Žentelis(AbCellera (Canada)), Lingshu Wang(National Institutes of Health), Denisa Foster(Eli Lilly (United States)), Peter Vaillancourt(Eli Lilly (United States)), Matthew Wiggin(AbCellera (Canada)), Erica Lovett(AbCellera (Canada)), Robin van der Lee(AbCellera (Canada)), J. Hendle(Eli Lilly (United States)), Anna Pustilnik(Eli Lilly (United States)), J.M. Sauder(Eli Lilly (United States)), Lucas Kraft(AbCellera (Canada)), Yuri Hwang(AbCellera (Canada)), Robert W. Siegel(Eli Lilly (United States)), Jinbiao Chen(Eli Lilly (United States)), Beverly A. Heinz(Eli Lilly (United States)), Richard E. Higgs(Eli Lilly (United States)), Nicole L. Kallewaard(Eli Lilly (United States)), Kevin R. Jepson(AbCellera (Canada)), Rodrigo Goya(AbCellera (Canada)), Maia A. Smith(AbCellera (Canada)), David W. Collins(AbCellera (Canada)), Davide Pellacani(AbCellera (Canada)), Ping Xiang(AbCellera (Canada)), Valentine de Puyraimond(AbCellera (Canada)), Markéta Řičicová(AbCellera (Canada)), Lindsay DeVorkin(AbCellera (Canada)), Caitlin Pritchard(AbCellera (Canada)), Aoise O’Neill(AbCellera (Canada)), Kush Dalal(AbCellera (Canada)), Pankaj Panwar(AbCellera (Canada)), Harveer Dhupar(AbCellera (Canada)), Fabian A. Garces(AbCellera (Canada)), Courtney A. Cohen(United States Army Medical Research Institute of Infectious Diseases), John M. Dye(United States Army Medical Research Institute of Infectious Diseases), Kathleen E. Huie(United States Army Medical Research Institute of Infectious Diseases), Catherine V. Badger(United States Army Medical Research Institute of Infectious Diseases), Darwyn Kobasa(Public Health Agency of Canada), Jonathan Audet(Public Health Agency of Canada), Joshua J. Freitas(Eli Lilly (United States)), Saleema Hassanali(Eli Lilly (United States)), Ina Hughes(Eli Lilly (United States)), Luis J. Muñoz(Eli Lilly (United States)), Holly C. Palma(Eli Lilly (United States)), Bharathi Ramamurthy(Eli Lilly (United States)), Robert W. Cross(University of Manitoba), Thomas W. Geisbert(University of Manitoba), Vineet D. Menachery(The University of Texas Medical Branch at Galveston), Kumari G. Lokugamage(The University of Texas Medical Branch at Galveston), Viktoriya Borisevich(The University of Texas Medical Branch at Galveston), Iliana Lanz(AbCellera (Canada)), Lisa K. Anderson(AbCellera (Canada)), Payal Sipahimalani(AbCellera (Canada)), Kizzmekia S. Corbett(National Institutes of Health), Eun Sung Yang(National Institutes of Health), Yi Zhang(National Institutes of Health), Wei Shi(National Institutes of Health), Tongqing Zhou(National Institutes of Health), Misook Choe(National Institutes of Health), John Misasi(National Institutes of Health), Peter D. Kwong(National Institutes of Health), Nancy J. Sullivan(National Institutes of Health), Barney S. Graham(National Institutes of Health), Tara L. Fernandez(AbCellera (Canada)), Carl L. Hansen(AbCellera (Canada)), Ester Falconer(AbCellera (Canada)), John R. Mascola(National Institutes of Health), Bryan E. Jones(Eli Lilly (United States)), Bryan C. Barnhart(AbCellera (Canada))
Cell Reports
April 25, 2022
Cited by 460Open Access
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Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-neutralizing monoclonal antibodies (mAbs) can reduce the risk of hospitalization from coronavirus disease 2019 (COVID-19) when administered early. However, SARS-CoV-2 variants of concern (VOCs) have negatively affected therapeutic use of some authorized mAbs. Using a high-throughput B cell screening pipeline, we isolated LY-CoV1404 (bebtelovimab), a highly potent SARS-CoV-2 spike glycoprotein receptor binding domain (RBD)-specific antibody. LY-CoV1404 potently neutralizes authentic SARS-CoV-2, B.1.1.7, B.1.351, and B.1.617.2. In pseudovirus neutralization studies, LY-CoV1404 potently neutralizes variants, including B.1.1.7, B.1.351, B.1.617.2, B.1.427/B.1.429, P.1, B.1.526, B.1.1.529, and the BA.2 subvariant. Structural analysis reveals that the contact residues of the LY-CoV1404 epitope are highly conserved, except for N439 and N501. The binding and neutralizing activity of LY-CoV1404 is unaffected by the most common mutations at these positions (N439K and N501Y). The broad and potent neutralization activity and the relatively conserved epitope suggest that LY-CoV1404 has the potential to be an effective therapeutic agent to treat all known variants.


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