Cargando…
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...
Autores principales: | , , , , , , , , |
---|---|
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 |
_version_ | 1785077868762497024 |
---|---|
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. |
format | Online Article Text |
id | pubmed-10369967 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT ketarennataliae nanobodyrepertoiregeneratedagainstthespikeproteinofancestralsarscov2remainsefficaciousagainsttherapidlyevolvingvirus AT mastfredd nanobodyrepertoiregeneratedagainstthespikeproteinofancestralsarscov2remainsefficaciousagainsttherapidlyevolvingvirus AT fridypeterc nanobodyrepertoiregeneratedagainstthespikeproteinofancestralsarscov2remainsefficaciousagainsttherapidlyevolvingvirus AT paulolivierjean nanobodyrepertoiregeneratedagainstthespikeproteinofancestralsarscov2remainsefficaciousagainsttherapidlyevolvingvirus AT sanyaltanmoy nanobodyrepertoiregeneratedagainstthespikeproteinofancestralsarscov2remainsefficaciousagainsttherapidlyevolvingvirus AT saliandrej nanobodyrepertoiregeneratedagainstthespikeproteinofancestralsarscov2remainsefficaciousagainsttherapidlyevolvingvirus AT chaitbriant nanobodyrepertoiregeneratedagainstthespikeproteinofancestralsarscov2remainsefficaciousagainsttherapidlyevolvingvirus AT routmichaelp nanobodyrepertoiregeneratedagainstthespikeproteinofancestralsarscov2remainsefficaciousagainsttherapidlyevolvingvirus AT aitchisonjohnd nanobodyrepertoiregeneratedagainstthespikeproteinofancestralsarscov2remainsefficaciousagainsttherapidlyevolvingvirus |