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A therapeutic neutralizing antibody targeting receptor binding domain of SARS-CoV-2 spike protein.
- Source :
-
Nature communications [Nat Commun] 2021 Jan 12; Vol. 12 (1), pp. 288. Date of Electronic Publication: 2021 Jan 12. - Publication Year :
- 2021
-
Abstract
- Vaccines and therapeutics are urgently needed for the pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Here, we screen human monoclonal antibodies (mAb) targeting the receptor binding domain (RBD) of the viral spike protein via antibody library constructed from peripheral blood mononuclear cells of a convalescent patient. The CT-P59 mAb potently neutralizes SARS-CoV-2 isolates including the D614G variant without antibody-dependent enhancement effect. Complex crystal structure of CT-P59 Fab/RBD shows that CT-P59 blocks interaction regions of RBD for angiotensin converting enzyme 2 (ACE2) receptor with an orientation that is notably different from previously reported RBD-targeting mAbs. Furthermore, therapeutic effects of CT-P59 are evaluated in three animal models (ferret, hamster, and rhesus monkey), demonstrating a substantial reduction in viral titer along with alleviation of clinical symptoms. Therefore, CT-P59 may be a promising therapeutic candidate for COVID-19.
- Subjects :
- Angiotensin-Converting Enzyme 2 chemistry
Animals
Antibodies, Monoclonal immunology
Antibodies, Neutralizing chemistry
Antibodies, Neutralizing immunology
Antibodies, Viral immunology
Chlorocebus aethiops
Disease Models, Animal
Female
Ferrets
Humans
Leukocytes, Mononuclear
Macaca mulatta
Male
Mesocricetus
Models, Molecular
Protein Conformation
Spike Glycoprotein, Coronavirus chemistry
Vero Cells
Antibodies, Neutralizing pharmacology
Protein Binding drug effects
SARS-CoV-2 drug effects
Spike Glycoprotein, Coronavirus drug effects
COVID-19 Drug Treatment
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 12
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 33436577
- Full Text :
- https://doi.org/10.1038/s41467-020-20602-5