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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...

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Autores principales: Entzminger, Kevin C, Fleming, Jonathan K, Entzminger, Paul D, Espinosa, Lisa Yuko, Samadi, Alex, Hiramoto, Yuko, Okumura, Shigeru C J, Maruyama, Toshiaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
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.
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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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