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Nanobody repertoire generated against the spike protein of ancestral SARS-CoV-2 remains efficacious against the rapidly evolving virus

To date, all major modes of monoclonal antibody therapy targeting SARS-CoV-2 have lost significant efficacy against the latest circulating variants. As SARS-CoV-2 omicron sublineages account for over 90% of COVID-19 infections, evasion of immune responses generated by vaccination or exposure to prev...

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Autores principales: Ketaren, Natalia E., Mast, Fred D., Fridy, Peter C., Paul Olivier, Jean, Sanyal, Tanmoy, Sali, Andrej, Chait, Brian T., Rout, Michael P., Aitchison, John D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10369967/
https://www.ncbi.nlm.nih.gov/pubmed/37503298
http://dx.doi.org/10.1101/2023.07.14.549041
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author Ketaren, Natalia E.
Mast, Fred D.
Fridy, Peter C.
Paul Olivier, Jean
Sanyal, Tanmoy
Sali, Andrej
Chait, Brian T.
Rout, Michael P.
Aitchison, John D.
author_facet Ketaren, Natalia E.
Mast, Fred D.
Fridy, Peter C.
Paul Olivier, Jean
Sanyal, Tanmoy
Sali, Andrej
Chait, Brian T.
Rout, Michael P.
Aitchison, John D.
author_sort Ketaren, Natalia E.
collection PubMed
description To date, all major modes of monoclonal antibody therapy targeting SARS-CoV-2 have lost significant efficacy against the latest circulating variants. As SARS-CoV-2 omicron sublineages account for over 90% of COVID-19 infections, evasion of immune responses generated by vaccination or exposure to previous variants poses a significant challenge. A compelling new therapeutic strategy against SARS-CoV-2 is that of single domain antibodies, termed nanobodies, which address certain limitations of monoclonal antibodies. Here we demonstrate that our high-affinity nanobody repertoire, generated against wild-type SARS-CoV-2 spike protein (Mast, Fridy et al. 2021), remains effective against variants of concern, including omicron BA.4/BA.5; a subset is predicted to counter resistance in emerging XBB and BQ.1.1 sublineages. Furthermore, we reveal the synergistic potential of nanobody cocktails in neutralizing emerging variants. Our study highlights the power of nanobody technology as a versatile therapeutic and diagnostic tool to combat rapidly evolving infectious diseases such as SARS-CoV-2.
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spelling pubmed-103699672023-07-27 Nanobody repertoire generated against the spike protein of ancestral SARS-CoV-2 remains efficacious against the rapidly evolving virus Ketaren, Natalia E. Mast, Fred D. Fridy, Peter C. Paul Olivier, Jean Sanyal, Tanmoy Sali, Andrej Chait, Brian T. Rout, Michael P. Aitchison, John D. bioRxiv Article To date, all major modes of monoclonal antibody therapy targeting SARS-CoV-2 have lost significant efficacy against the latest circulating variants. As SARS-CoV-2 omicron sublineages account for over 90% of COVID-19 infections, evasion of immune responses generated by vaccination or exposure to previous variants poses a significant challenge. A compelling new therapeutic strategy against SARS-CoV-2 is that of single domain antibodies, termed nanobodies, which address certain limitations of monoclonal antibodies. Here we demonstrate that our high-affinity nanobody repertoire, generated against wild-type SARS-CoV-2 spike protein (Mast, Fridy et al. 2021), remains effective against variants of concern, including omicron BA.4/BA.5; a subset is predicted to counter resistance in emerging XBB and BQ.1.1 sublineages. Furthermore, we reveal the synergistic potential of nanobody cocktails in neutralizing emerging variants. Our study highlights the power of nanobody technology as a versatile therapeutic and diagnostic tool to combat rapidly evolving infectious diseases such as SARS-CoV-2. Cold Spring Harbor Laboratory 2023-07-14 /pmc/articles/PMC10369967/ /pubmed/37503298 http://dx.doi.org/10.1101/2023.07.14.549041 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Ketaren, Natalia E.
Mast, Fred D.
Fridy, Peter C.
Paul Olivier, Jean
Sanyal, Tanmoy
Sali, Andrej
Chait, Brian T.
Rout, Michael P.
Aitchison, John D.
Nanobody repertoire generated against the spike protein of ancestral SARS-CoV-2 remains efficacious against the rapidly evolving virus
title Nanobody repertoire generated against the spike protein of ancestral SARS-CoV-2 remains efficacious against the rapidly evolving virus
title_full Nanobody repertoire generated against the spike protein of ancestral SARS-CoV-2 remains efficacious against the rapidly evolving virus
title_fullStr Nanobody repertoire generated against the spike protein of ancestral SARS-CoV-2 remains efficacious against the rapidly evolving virus
title_full_unstemmed Nanobody repertoire generated against the spike protein of ancestral SARS-CoV-2 remains efficacious against the rapidly evolving virus
title_short Nanobody repertoire generated against the spike protein of ancestral SARS-CoV-2 remains efficacious against the rapidly evolving virus
title_sort nanobody repertoire generated against the spike protein of ancestral sars-cov-2 remains efficacious against the rapidly evolving virus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10369967/
https://www.ncbi.nlm.nih.gov/pubmed/37503298
http://dx.doi.org/10.1101/2023.07.14.549041
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