Vanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN, USA.
Pre-Clinical Vaccine Development, Infectious Disease Research Institute, Seattle, WA, USA.
Nat Biomed Eng. 2020 Nov;4(11):1030-1043. doi: 10.1038/s41551-020-0594-x. Epub 2020 Aug 3.
The emergence and re-emergence of highly virulent viral pathogens with the potential to cause a pandemic creates an urgent need for the accelerated discovery of antiviral therapeutics. Antiviral human monoclonal antibodies (mAbs) are promising candidates for the prevention and treatment of severe viral diseases, but their long development timeframes limit their rapid deployment and use. Here, we report the development of an integrated sequence of technologies, including single-cell mRNA-sequence analysis, bioinformatics, synthetic biology and high-throughput functional analysis, that enables the rapid discovery of highly potent antiviral human mAbs, the activity of which we validated in vivo. In a 78-d study modelling the deployment of a rapid response to an outbreak, we isolated more than 100 human mAbs that are specific to Zika virus, assessed their function, identified that 29 of these mAbs have broadly neutralizing activity, and verified the therapeutic potency of the lead candidates in mice and non-human primate models of infection through the delivery of an antibody-encoding mRNA formulation and of the respective IgG antibody. The pipeline provides a roadmap for rapid antibody-discovery programmes against viral pathogens of global concern.
高毒力病毒病原体的出现和再现,有可能导致大流行,这就迫切需要加速发现抗病毒疗法。抗病毒的人源单克隆抗体(mAbs)是预防和治疗严重病毒性疾病的有希望的候选药物,但它们的开发时间长,限制了它们的快速部署和使用。在这里,我们报告了一系列集成技术的开发,包括单细胞 mRNA 序列分析、生物信息学、合成生物学和高通量功能分析,这些技术能够快速发现高效的抗病毒人源 mAbs,我们在体内验证了它们的活性。在一项模拟对疫情快速反应部署的 78 天研究中,我们分离出了 100 多种针对寨卡病毒的人源 mAbs,评估了它们的功能,确定其中 29 种 mAbs 具有广谱中和活性,并通过递送抗体编码 mRNA 制剂和相应的 IgG 抗体,在感染的小鼠和非人类灵长类动物模型中验证了候选药物的治疗效力。该流水线为针对具有全球关注的病毒病原体的快速抗体发现计划提供了路线图。