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

Q2 Medicine Antibody Therapeutics Pub Date : 2023-04-01 DOI:10.1093/abt/tbad003
Huabing Yang, Yuxin Chen, Dongcheng Jiang, Xiaoli Feng, Ying Xu, Jiayu Wei, Qingcui Zou, Qiaojiang Yang, Jihong Chen, Xiaoling Jiang, Chunling Qin, Zhenzhen Huang, Chongbing Wu, Ying Zhou, Minghua Li, Liusong Yin
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Abstract

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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具有长期保护作用的抗SARS-CoV-2四价宽中和双特异性抗体ISH0339的临床前评价
背景:结束全球COVID-19大流行需要针对严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)的有效治疗。然而,新出现的Omicron亚谱系在很大程度上逃脱了当前授权的单克隆抗体治疗的中和。在这里,我们报告了一种四价双特异性抗体ISH0339,作为长期和广泛保护COVID-19的潜在候选抗体。方法:我们在此报道了ISH0339的制备,ISH0339是一种新型四价双特异性抗体,由一对非竞争性中和抗体组成,可特异性结合SARS-CoV-2受体结合域(RBD)的两个不同中和表位,并含有一个工程Fc区,可延长抗体半衰期。我们描述了ISH0339的临床前特征,并讨论了其作为预防和治疗SARS-CoV-2感染的新型药物的潜力。结果:ISH0339以高亲和力特异性结合SARS-CoV-2 RBD,有效阻断RBD与宿主受体hACE2的结合。ISH0339表现出比亲本单克隆抗体更高的结合、阻断和中和效率,并保留了对所有检测的SARS-CoV-2变体的中和能力。单次给药ISH0339在静脉注射治疗和鼻喷剂预防中显示出有效的中和活性。单次给药ISH0339后的临床前研究显示出良好的药代动力学和耐受性良好的毒理学特征。结论:ISH0339已显示出良好的安全性和对所有当前关注的sars - cov -2变体的有效抗活性。此外,预防性和治疗性应用ISH0339可显著降低肺部病毒滴度。用于评估ISH0339预防和治疗SARS-CoV-2感染的安全性、耐受性和初步疗效的研究性新药研究已经提交。
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来源期刊
Antibody Therapeutics
Antibody Therapeutics Medicine-Immunology and Allergy
CiteScore
8.70
自引率
0.00%
发文量
30
审稿时长
8 weeks
期刊最新文献
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