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Rapid identification of a human antibody with high prophylactic and therapeutic efficacy in three animal models of SARS-CoV-2 infection.
- Source :
-
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2020 Nov 24; Vol. 117 (47), pp. 29832-29838. Date of Electronic Publication: 2020 Nov 02. - Publication Year :
- 2020
-
Abstract
- Effective therapies are urgently needed for the SARS-CoV-2/COVID-19 pandemic. We identified panels of fully human monoclonal antibodies (mAbs) from large phage-displayed Fab, scFv, and VH libraries by panning against the receptor binding domain (RBD) of the SARS-CoV-2 spike (S) glycoprotein. A high-affinity Fab was selected from one of the libraries and converted to a full-size antibody, IgG1 ab1, which competed with human ACE2 for binding to RBD. It potently neutralized replication-competent SARS-CoV-2 but not SARS-CoV, as measured by two different tissue culture assays, as well as a replication-competent mouse ACE2-adapted SARS-CoV-2 in BALB/c mice and native virus in hACE2-expressing transgenic mice showing activity at the lowest tested dose of 2 mg/kg. IgG1 ab1 also exhibited high prophylactic and therapeutic efficacy in a hamster model of SARS-CoV-2 infection. The mechanism of neutralization is by competition with ACE2 but could involve antibody-dependent cellular cytotoxicity (ADCC) as IgG1 ab1 had ADCC activity in vitro. The ab1 sequence has a relatively low number of somatic mutations, indicating that ab1-like antibodies could be quickly elicited during natural SARS-CoV-2 infection or by RBD-based vaccines. IgG1 ab1 did not aggregate, did not exhibit other developability liabilities, and did not bind to any of the 5,300 human membrane-associated proteins tested. These results suggest that IgG1 ab1 has potential for therapy and prophylaxis of SARS-CoV-2 infections. The rapid identification (within 6 d of availability of antigen for panning) of potent mAbs shows the value of large antibody libraries for response to public health threats from emerging microbes.<br />Competing Interests: Competing interest statement: W.L., C.C., Z.S., D.V.Z., J.W.M., and D.S.D. are coinventors of a patent, filed by the University of Pittsburgh on March 12, 2020, related to antibodies described in this paper. E.C.P., A.C., J.W.M., and D.S.D. are employed by Abound Bio, a company which is developing some of the antibodies for human use.<br /> (Copyright © 2020 the Author(s). Published by PNAS.)
- Subjects :
- Angiotensin-Converting Enzyme 2 metabolism
Animals
Antibodies, Viral blood
Antibodies, Viral immunology
Antibody-Dependent Cell Cytotoxicity
COVID-19 Serological Testing standards
COVID-19 Vaccines standards
Chlorocebus aethiops
Cricetinae
Female
Humans
Immunization, Passive methods
Immunization, Passive standards
Immunogenicity, Vaccine
Immunoglobulin G blood
Immunoglobulin G immunology
Mice
Mice, Inbred BALB C
SARS-CoV-2 immunology
Spike Glycoprotein, Coronavirus chemistry
Spike Glycoprotein, Coronavirus immunology
Vero Cells
COVID-19 Serotherapy
COVID-19 therapy
COVID-19 Serological Testing methods
COVID-19 Vaccines immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1091-6490
- Volume :
- 117
- Issue :
- 47
- Database :
- MEDLINE
- Journal :
- Proceedings of the National Academy of Sciences of the United States of America
- Publication Type :
- Academic Journal
- Accession number :
- 33139569
- Full Text :
- https://doi.org/10.1073/pnas.2010197117