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Comprehensive engineering of a therapeutic neutralizing antibody targeting SARS-CoV-2 spike protein to neutralize escape variants
The emergence of escape variants of SARS-CoV-2 carrying mutations in the spike protein poses a challenge for therapeutic antibodies. Here, we show that through the comprehensive engineering of the variable region of the neutralizing monoclonal antibody 5A6, the engineered antibody, 5A6CCS1, is able...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8932922/ https://www.ncbi.nlm.nih.gov/pubmed/35293276 http://dx.doi.org/10.1080/19420862.2022.2040350 |
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author | Kuramochi, Taichi Gan, Siok Wan Ho, Adrian W.S. Wang, Bei Kageji, Nagisa Nambu, Takeru Iida, Sayaka Okuda-Miura, Momoko Chia, Wei Shan Yeo, Chiew Ying Chen, Dan Lee, Wen-Hsin Ngoh, Eve Zi Xian Mohd Salleh, Siti Nazihah Wang, Cheng-I Igawa, Tomoyuki Shimada, Hideaki |
author_facet | Kuramochi, Taichi Gan, Siok Wan Ho, Adrian W.S. Wang, Bei Kageji, Nagisa Nambu, Takeru Iida, Sayaka Okuda-Miura, Momoko Chia, Wei Shan Yeo, Chiew Ying Chen, Dan Lee, Wen-Hsin Ngoh, Eve Zi Xian Mohd Salleh, Siti Nazihah Wang, Cheng-I Igawa, Tomoyuki Shimada, Hideaki |
author_sort | Kuramochi, Taichi |
collection | PubMed |
description | The emergence of escape variants of SARS-CoV-2 carrying mutations in the spike protein poses a challenge for therapeutic antibodies. Here, we show that through the comprehensive engineering of the variable region of the neutralizing monoclonal antibody 5A6, the engineered antibody, 5A6CCS1, is able to neutralize SARS-CoV-2 variants that escaped neutralization by the original 5A6 antibody. In addition to the improved affinity against variants, 5A6CCS1 was also optimized to achieve high solubility and low viscosity, enabling a high concentration formulation for subcutaneous injection. In cynomolgus monkeys, 5A6CCS1 showed a long plasma half-life and good subcutaneous bioavailability through engineering of the variable and constant region. These data demonstrate that 5A6CCS1 is a promising antibody for development against SARS-CoV-2 and highlight the importance of antibody engineering as a potential method to counteract escape variants. |
format | Online Article Text |
id | pubmed-8932922 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-89329222022-03-19 Comprehensive engineering of a therapeutic neutralizing antibody targeting SARS-CoV-2 spike protein to neutralize escape variants Kuramochi, Taichi Gan, Siok Wan Ho, Adrian W.S. Wang, Bei Kageji, Nagisa Nambu, Takeru Iida, Sayaka Okuda-Miura, Momoko Chia, Wei Shan Yeo, Chiew Ying Chen, Dan Lee, Wen-Hsin Ngoh, Eve Zi Xian Mohd Salleh, Siti Nazihah Wang, Cheng-I Igawa, Tomoyuki Shimada, Hideaki MAbs Report The emergence of escape variants of SARS-CoV-2 carrying mutations in the spike protein poses a challenge for therapeutic antibodies. Here, we show that through the comprehensive engineering of the variable region of the neutralizing monoclonal antibody 5A6, the engineered antibody, 5A6CCS1, is able to neutralize SARS-CoV-2 variants that escaped neutralization by the original 5A6 antibody. In addition to the improved affinity against variants, 5A6CCS1 was also optimized to achieve high solubility and low viscosity, enabling a high concentration formulation for subcutaneous injection. In cynomolgus monkeys, 5A6CCS1 showed a long plasma half-life and good subcutaneous bioavailability through engineering of the variable and constant region. These data demonstrate that 5A6CCS1 is a promising antibody for development against SARS-CoV-2 and highlight the importance of antibody engineering as a potential method to counteract escape variants. Taylor & Francis 2022-03-16 /pmc/articles/PMC8932922/ /pubmed/35293276 http://dx.doi.org/10.1080/19420862.2022.2040350 Text en © 2022 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Report Kuramochi, Taichi Gan, Siok Wan Ho, Adrian W.S. Wang, Bei Kageji, Nagisa Nambu, Takeru Iida, Sayaka Okuda-Miura, Momoko Chia, Wei Shan Yeo, Chiew Ying Chen, Dan Lee, Wen-Hsin Ngoh, Eve Zi Xian Mohd Salleh, Siti Nazihah Wang, Cheng-I Igawa, Tomoyuki Shimada, Hideaki Comprehensive engineering of a therapeutic neutralizing antibody targeting SARS-CoV-2 spike protein to neutralize escape variants |
title | Comprehensive engineering of a therapeutic neutralizing antibody targeting SARS-CoV-2 spike protein to neutralize escape variants |
title_full | Comprehensive engineering of a therapeutic neutralizing antibody targeting SARS-CoV-2 spike protein to neutralize escape variants |
title_fullStr | Comprehensive engineering of a therapeutic neutralizing antibody targeting SARS-CoV-2 spike protein to neutralize escape variants |
title_full_unstemmed | Comprehensive engineering of a therapeutic neutralizing antibody targeting SARS-CoV-2 spike protein to neutralize escape variants |
title_short | Comprehensive engineering of a therapeutic neutralizing antibody targeting SARS-CoV-2 spike protein to neutralize escape variants |
title_sort | comprehensive engineering of a therapeutic neutralizing antibody targeting sars-cov-2 spike protein to neutralize escape variants |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8932922/ https://www.ncbi.nlm.nih.gov/pubmed/35293276 http://dx.doi.org/10.1080/19420862.2022.2040350 |
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