Kevin C Entzminger, Jonathan K Fleming, Paul D Entzminger, Lisa Yuko Espinosa, Alex Samadi, Yuko Hiramoto, Shigeru C J Okumura, Toshiaki Maruyama
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引用次数: 2
摘要
即使对完全接种疫苗的个体,SARS-CoV-2 Omicron变体XBB.1.5也显示出非凡的免疫逃逸。目前还没有被批准的抗体来中和这种变异,而新变异的不断出现使免疫功能低下和老年患者处于高风险之中。迫切需要快速和经济有效地开发中和抗体。从中和武汉- hu -1菌株的单亲本克隆开始,抗体工程在使用称为阶段增强成熟的专有技术的变体出现时实时进行迭代阶段。通过噬菌体展示的体外亲和成熟获得了广泛中和当前循环的Omicron变体的抗体面板。通过替代病毒中和试验和对所有变异的pM KD亲和力,工程抗体表现出对BQ.1.1、XBB.1.16和XBB.1.5的有效中和。我们的工作不仅详细介绍了新的候选治疗方法,而且验证了一种独特的一般策略,可以创建针对当前和未来SARS-CoV-2变体的广泛中和抗体。
Rapid engineering of SARS-CoV-2 therapeutic antibodies to increase breadth of neutralization including BQ.1.1, CA.3.1, CH.1.1, XBB.1.16, and XBB.1.5.
SARS-CoV-2 Omicron variant XBB.1.5 has shown extraordinary immune escape even for fully vaccinated individuals. There are currently no approved antibodies that neutralize this variant, and continued emergence of new variants puts immunocompromised and elderly patients at high risk. Rapid and cost-effective development of neutralizing antibodies is urgently needed. Starting with a single parent clone that neutralized the Wuhan-Hu-1 strain, antibody engineering was performed in iterative stages in real time as variants emerged using a proprietary technology called STage-Enhanced Maturation. An antibody panel that broadly neutralizes currently circulating Omicron variants was obtained by in vitro affinity maturation using phage display. The engineered antibodies show potent neutralization of BQ.1.1, XBB.1.16, and XBB.1.5 by surrogate virus neutralization test and pM KD affinity for all variants. Our work not only details novel therapeutic candidates but also validates a unique general strategy to create broadly neutralizing antibodies to current and future SARS-CoV-2 variants.