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

Author:

Yang Huabing1,Chen Yuxin2,Jiang Dongcheng1,Feng Xiaoli3,Xu Ying4,Wei Jiayu4,Zou Qingcui3,Yang Qiaojiang3,Chen Jihong1,Jiang Xiaoling1,Qin Chunling1,Huang Zhenzhen1,Wu Chongbing1,Zhou Ying1,Li Minghua3,Yin Liusong1

Affiliation:

1. SunHo (China) BioPharmaceutical Co., Ltd. , No.5 Xingjian Road, Economic and Technological Development Zone, Nanjing 210046, Jiangsu , China

2. Nanjing University Medical School Department of Laboratory Medicine, Nanjing Drum Tower Hospital, , Nanjing 210008, Jiangsu , China

3. Chinese Academy of Sciences Kunming National High-level Biosafety Research Center for Non-Human Primates, Center for Biosafety Mega-Science, Kunming Institute of Zoology, , Kunming 650107, Yunnan , China

4. Nanjing Agricultural University College of Life Sciences, , Nanjing 210095, Jiangsu , China

Abstract

AbstractBackground: 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.

Funder

SunHo (China) BioPharmaceutical Co., Ltd

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

Reference27 articles.

1. A broadly neutralizing humanized ACE2-targeting antibody against SARS-CoV-2 variants;Du;Nat Commun,2021

2. In vivo monoclonal antibody efficacy against SARS-CoV-2 variant strains;Chen;Nature,2021

3. SARS-CoV-2 Omicron-B.1.1.529 leads to widespread escape from neutralizing antibody responses;Dejnirattisai

4. Therapeutic antibodies and fusion inhibitors targeting the spike protein of SARS-CoV-2;Jiang;Expert Opin Ther Targets,2021

5. SARS-CoV-2 neutralizing antibody structures inform therapeutic strategies;Barnes;Nature,2020

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3