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Rapid engineering of SARS-CoV-2 therapeutic antibodies to increase breadth of neutralization including BQ.1.1, CA.3.1, CH.1.1, XBB.1.16, and XBB.1.5
SARS-CoV-2 Omicron variant XBB.1.5 has shown extraordinary immune escape even for fully vaccinated individuals. There are currently no approved antibodies that neutralize this variant, and continued emergence of new variants puts immunocompromised and elderly patients at high risk. Rapid and cost-ef...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10262839/ https://www.ncbi.nlm.nih.gov/pubmed/37324547 http://dx.doi.org/10.1093/abt/tbad006 |
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author | Entzminger, Kevin C Fleming, Jonathan K Entzminger, Paul D Espinosa, Lisa Yuko Samadi, Alex Hiramoto, Yuko Okumura, Shigeru C J Maruyama, Toshiaki |
author_facet | Entzminger, Kevin C Fleming, Jonathan K Entzminger, Paul D Espinosa, Lisa Yuko Samadi, Alex Hiramoto, Yuko Okumura, Shigeru C J Maruyama, Toshiaki |
author_sort | Entzminger, Kevin C |
collection | PubMed |
description | SARS-CoV-2 Omicron variant XBB.1.5 has shown extraordinary immune escape even for fully vaccinated individuals. There are currently no approved antibodies that neutralize this variant, and continued emergence of new variants puts immunocompromised and elderly patients at high risk. Rapid and cost-effective development of neutralizing antibodies is urgently needed. Starting with a single parent clone that neutralized the Wuhan-Hu-1 strain, antibody engineering was performed in iterative stages in real time as variants emerged using a proprietary technology called STage-Enhanced Maturation. An antibody panel that broadly neutralizes currently circulating Omicron variants was obtained by in vitro affinity maturation using phage display. The engineered antibodies show potent neutralization of BQ.1.1, XBB.1.16, and XBB.1.5 by surrogate virus neutralization test and pM K(D) affinity for all variants. Our work not only details novel therapeutic candidates but also validates a unique general strategy to create broadly neutralizing antibodies to current and future SARS-CoV-2 variants. |
format | Online Article Text |
id | pubmed-10262839 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-102628392023-06-15 Rapid engineering of SARS-CoV-2 therapeutic antibodies to increase breadth of neutralization including BQ.1.1, CA.3.1, CH.1.1, XBB.1.16, and XBB.1.5 Entzminger, Kevin C Fleming, Jonathan K Entzminger, Paul D Espinosa, Lisa Yuko Samadi, Alex Hiramoto, Yuko Okumura, Shigeru C J Maruyama, Toshiaki Antib Ther Research Article SARS-CoV-2 Omicron variant XBB.1.5 has shown extraordinary immune escape even for fully vaccinated individuals. There are currently no approved antibodies that neutralize this variant, and continued emergence of new variants puts immunocompromised and elderly patients at high risk. Rapid and cost-effective development of neutralizing antibodies is urgently needed. Starting with a single parent clone that neutralized the Wuhan-Hu-1 strain, antibody engineering was performed in iterative stages in real time as variants emerged using a proprietary technology called STage-Enhanced Maturation. An antibody panel that broadly neutralizes currently circulating Omicron variants was obtained by in vitro affinity maturation using phage display. The engineered antibodies show potent neutralization of BQ.1.1, XBB.1.16, and XBB.1.5 by surrogate virus neutralization test and pM K(D) affinity for all variants. Our work not only details novel therapeutic candidates but also validates a unique general strategy to create broadly neutralizing antibodies to current and future SARS-CoV-2 variants. Oxford University Press 2023-04-13 /pmc/articles/PMC10262839/ /pubmed/37324547 http://dx.doi.org/10.1093/abt/tbad006 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Antibody Therapeutics. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Entzminger, Kevin C Fleming, Jonathan K Entzminger, Paul D Espinosa, Lisa Yuko Samadi, Alex Hiramoto, Yuko Okumura, Shigeru C J Maruyama, Toshiaki Rapid engineering of SARS-CoV-2 therapeutic antibodies to increase breadth of neutralization including BQ.1.1, CA.3.1, CH.1.1, XBB.1.16, and XBB.1.5 |
title | Rapid engineering of SARS-CoV-2 therapeutic antibodies to increase breadth of neutralization including BQ.1.1, CA.3.1, CH.1.1, XBB.1.16, and XBB.1.5 |
title_full | Rapid engineering of SARS-CoV-2 therapeutic antibodies to increase breadth of neutralization including BQ.1.1, CA.3.1, CH.1.1, XBB.1.16, and XBB.1.5 |
title_fullStr | Rapid engineering of SARS-CoV-2 therapeutic antibodies to increase breadth of neutralization including BQ.1.1, CA.3.1, CH.1.1, XBB.1.16, and XBB.1.5 |
title_full_unstemmed | Rapid engineering of SARS-CoV-2 therapeutic antibodies to increase breadth of neutralization including BQ.1.1, CA.3.1, CH.1.1, XBB.1.16, and XBB.1.5 |
title_short | Rapid engineering of SARS-CoV-2 therapeutic antibodies to increase breadth of neutralization including BQ.1.1, CA.3.1, CH.1.1, XBB.1.16, and XBB.1.5 |
title_sort | rapid engineering of sars-cov-2 therapeutic antibodies to increase breadth of neutralization including bq.1.1, ca.3.1, ch.1.1, xbb.1.16, and xbb.1.5 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10262839/ https://www.ncbi.nlm.nih.gov/pubmed/37324547 http://dx.doi.org/10.1093/abt/tbad006 |
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