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A pandemic-enabled comparison of discovery platforms demonstrates a naïve antibody library can match the best immune-sourced antibodies.
- Source :
-
Nature communications [Nat Commun] 2022 Jan 24; Vol. 13 (1), pp. 462. Date of Electronic Publication: 2022 Jan 24. - Publication Year :
- 2022
-
Abstract
- As a result of the SARS-CoV-2 pandemic numerous scientific groups have generated antibodies against a single target: the CoV-2 spike antigen. This has provided an unprecedented opportunity to compare the efficacy of different methods and the specificities and qualities of the antibodies generated by those methods. Generally, the most potent neutralizing antibodies have been generated from convalescent patients and immunized animals, with non-immune phage libraries usually yielding significantly less potent antibodies. Here, we show that it is possible to generate ultra-potent (IC <subscript>50</subscript> < 2 ng/ml) human neutralizing antibodies directly from a unique semisynthetic naïve antibody library format with affinities, developability properties and neutralization activities comparable to the best from hyperimmune sources. This demonstrates that appropriately designed and constructed naïve antibody libraries can effectively compete with immunization to directly provide therapeutic antibodies against a viral pathogen, without the need for immune sources or downstream optimization.<br /> (© 2022. The Author(s).)
- Subjects :
- Animals
Antibodies, Monoclonal immunology
Antibodies, Monoclonal metabolism
Antibody Affinity immunology
COVID-19 epidemiology
COVID-19 virology
Chlorocebus aethiops
Humans
Immunoglobulin G immunology
Immunoglobulin G metabolism
Neutralization Tests methods
Pandemics
Peptide Library
Protein Binding
SARS-CoV-2 metabolism
SARS-CoV-2 physiology
Single-Chain Antibodies immunology
Single-Chain Antibodies metabolism
Spike Glycoprotein, Coronavirus metabolism
Vero Cells
Antibodies, Neutralizing immunology
Antibodies, Viral immunology
COVID-19 immunology
SARS-CoV-2 immunology
Spike Glycoprotein, Coronavirus immunology
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 13
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 35075126
- Full Text :
- https://doi.org/10.1038/s41467-021-27799-z