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Preclinical evaluation of ISH0339, a tetravalent broadly neutralizing bispecific antibody against SARS-CoV-2 with long-term protection

Background: Ending the global COVID-19 pandemic requires efficacious therapies against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Nevertheless, the emerging Omicron sublineages largely escaped the neutralization of current authorized monoclonal antibody therapies. Here we report a...

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Autores principales: Yang, Huabing, Chen, Yuxin, Jiang, Dongcheng, Feng, Xiaoli, Xu, Ying, Wei, Jiayu, Zou, Qingcui, Yang, Qiaojiang, Chen, Jihong, Jiang, Xiaoling, Qin, Chunling, Huang, Zhenzhen, Wu, Chongbing, Zhou, Ying, Li, Minghua, Yin, Liusong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10108555/
https://www.ncbi.nlm.nih.gov/pubmed/37077474
http://dx.doi.org/10.1093/abt/tbad003
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author Yang, Huabing
Chen, Yuxin
Jiang, Dongcheng
Feng, Xiaoli
Xu, Ying
Wei, Jiayu
Zou, Qingcui
Yang, Qiaojiang
Chen, Jihong
Jiang, Xiaoling
Qin, Chunling
Huang, Zhenzhen
Wu, Chongbing
Zhou, Ying
Li, Minghua
Yin, Liusong
author_facet Yang, Huabing
Chen, Yuxin
Jiang, Dongcheng
Feng, Xiaoli
Xu, Ying
Wei, Jiayu
Zou, Qingcui
Yang, Qiaojiang
Chen, Jihong
Jiang, Xiaoling
Qin, Chunling
Huang, Zhenzhen
Wu, Chongbing
Zhou, Ying
Li, Minghua
Yin, Liusong
author_sort Yang, Huabing
collection PubMed
description Background: Ending the global COVID-19 pandemic requires efficacious therapies against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Nevertheless, the emerging Omicron sublineages largely escaped the neutralization of current authorized monoclonal antibody therapies. Here we report a tetravalent bispecific antibody ISH0339, as a potential candidate for long-term and broad protection against COVID-19. Methods: We report here the making of ISH0339, a novel tetravalent bispecific antibody composed of a pair of non-competing neutralizing antibodies that binds specifically to two different neutralizing epitopes of SARS-CoV-2 receptor-binding domain (RBD) and contains an engineered Fc region for prolonged antibody half-life. We describe the preclinical characterization of ISH0339 and discuss its potential as a novel agent for both prophylactic and therapeutic purposes against SARS-CoV-2 infection. Results: ISH0339 bound to SARS-CoV-2 RBD specifically with high affinity and potently blocked the binding of RBD to the host receptor hACE2. ISH0339 demonstrated greater binding, blocking and neutralizing efficiency than its parental monoclonal antibodies, and retained neutralizing ability to all tested SARS-CoV-2 variants of concern. Single dosing of ISH0339 showed potent neutralizing activity for treatment via intravenous injection and for prophylaxis via nasal spray. Preclinical studies following single dosing of ISH0339 showed favorable pharmacokinetics and well-tolerated toxicology profile. Conclusion: ISH0339 has demonstrated a favorable safety profile and potent anti-SARS-CoV-2 activities against all current variants of concern. Furthermore, prophylactic and therapeutic application of ISH0339 significantly reduced the viral titer in lungs. Investigational New Drug studies to evaluate the safety, tolerability and preliminary efficacy of ISH0339 for both prophylactic and therapeutic purposes against SARS-CoV-2 infection have been filed.
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spelling pubmed-101085552023-04-18 Preclinical evaluation of ISH0339, a tetravalent broadly neutralizing bispecific antibody against SARS-CoV-2 with long-term protection Yang, Huabing Chen, Yuxin Jiang, Dongcheng Feng, Xiaoli Xu, Ying Wei, Jiayu Zou, Qingcui Yang, Qiaojiang Chen, Jihong Jiang, Xiaoling Qin, Chunling Huang, Zhenzhen Wu, Chongbing Zhou, Ying Li, Minghua Yin, Liusong Antib Ther Research Article Background: Ending the global COVID-19 pandemic requires efficacious therapies against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Nevertheless, the emerging Omicron sublineages largely escaped the neutralization of current authorized monoclonal antibody therapies. Here we report a tetravalent bispecific antibody ISH0339, as a potential candidate for long-term and broad protection against COVID-19. Methods: We report here the making of ISH0339, a novel tetravalent bispecific antibody composed of a pair of non-competing neutralizing antibodies that binds specifically to two different neutralizing epitopes of SARS-CoV-2 receptor-binding domain (RBD) and contains an engineered Fc region for prolonged antibody half-life. We describe the preclinical characterization of ISH0339 and discuss its potential as a novel agent for both prophylactic and therapeutic purposes against SARS-CoV-2 infection. Results: ISH0339 bound to SARS-CoV-2 RBD specifically with high affinity and potently blocked the binding of RBD to the host receptor hACE2. ISH0339 demonstrated greater binding, blocking and neutralizing efficiency than its parental monoclonal antibodies, and retained neutralizing ability to all tested SARS-CoV-2 variants of concern. Single dosing of ISH0339 showed potent neutralizing activity for treatment via intravenous injection and for prophylaxis via nasal spray. Preclinical studies following single dosing of ISH0339 showed favorable pharmacokinetics and well-tolerated toxicology profile. Conclusion: ISH0339 has demonstrated a favorable safety profile and potent anti-SARS-CoV-2 activities against all current variants of concern. Furthermore, prophylactic and therapeutic application of ISH0339 significantly reduced the viral titer in lungs. Investigational New Drug studies to evaluate the safety, tolerability and preliminary efficacy of ISH0339 for both prophylactic and therapeutic purposes against SARS-CoV-2 infection have been filed. Oxford University Press 2023-03-06 /pmc/articles/PMC10108555/ /pubmed/37077474 http://dx.doi.org/10.1093/abt/tbad003 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Antibody Therapeutics. All rights reserved. For Permissions, please email: journals.permissions@oup.com https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Yang, Huabing
Chen, Yuxin
Jiang, Dongcheng
Feng, Xiaoli
Xu, Ying
Wei, Jiayu
Zou, Qingcui
Yang, Qiaojiang
Chen, Jihong
Jiang, Xiaoling
Qin, Chunling
Huang, Zhenzhen
Wu, Chongbing
Zhou, Ying
Li, Minghua
Yin, Liusong
Preclinical evaluation of ISH0339, a tetravalent broadly neutralizing bispecific antibody against SARS-CoV-2 with long-term protection
title Preclinical evaluation of ISH0339, a tetravalent broadly neutralizing bispecific antibody against SARS-CoV-2 with long-term protection
title_full Preclinical evaluation of ISH0339, a tetravalent broadly neutralizing bispecific antibody against SARS-CoV-2 with long-term protection
title_fullStr Preclinical evaluation of ISH0339, a tetravalent broadly neutralizing bispecific antibody against SARS-CoV-2 with long-term protection
title_full_unstemmed Preclinical evaluation of ISH0339, a tetravalent broadly neutralizing bispecific antibody against SARS-CoV-2 with long-term protection
title_short Preclinical evaluation of ISH0339, a tetravalent broadly neutralizing bispecific antibody against SARS-CoV-2 with long-term protection
title_sort preclinical evaluation of ish0339, a tetravalent broadly neutralizing bispecific antibody against sars-cov-2 with long-term protection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10108555/
https://www.ncbi.nlm.nih.gov/pubmed/37077474
http://dx.doi.org/10.1093/abt/tbad003
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