Back to Search Start Over

Rapid identification of a human antibody with high prophylactic and therapeutic efficacy in three animal models of SARS-CoV-2 infection.

Authors :
Li W
Chen C
Drelich A
Martinez DR
Gralinski LE
Sun Z
Schäfer A
Kulkarni SS
Liu X
Leist SR
Zhelev DV
Zhang L
Kim YJ
Peterson EC
Conard A
Mellors JW
Tseng CK
Falzarano D
Baric RS
Dimitrov DS
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.)

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