中和
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
2019年冠状病毒病(COVID-19)
抗体
2019-20冠状病毒爆发
病毒学
类有机物
Sars病毒
生物
计算生物学
医学
免疫学
传染病(医学专业)
遗传学
病理
疾病
爆发
作者
Zhixin Wan,Cun Li,Ying Zhou,Yifei Yu,Man Chun Chiu,Jingjing Huang,Shuxin Zhang,Xiaoxin Zhu,Qiaoshuai Lan,Yanlin Deng,Weiwei Xue,Chengfan Jiang,Jiali Wu,Zijun Zhao,Jian‐Piao Cai,Lin Huang,Yong Zhang,Xiaojuan Liu,Zheng Zhang,Hin Chu
标识
DOI:10.1073/pnas.2509616122
摘要
The efficacy of VIR-7831, a class 3 anti-SARS-CoV-2 monoclonal antibody (mAb), was demonstrated repeatedly in clinical trials; yet, reduced neutralization against Omicron variants in cell-line-based neutralization assays led to its withdrawal from clinical use. We developed organoid-based neutralization assays to measure mAb potency. We found that most class 3 mAbs, especially those not blocking receptor-binding domain-ACE2 binding, including VIR-7831, were substantially underestimated in cell-line-based assays. Nasal organoids adequately recapitulated the real-world effectiveness of VIR-7831 because of biologically relevant low ACE2 expression, and exclusively reproduced the in vivo protection of S2 mAbs due to the high TMPRSS2 expression, reminiscent of native human respiratory epithelial cells. Collectively, the robust organoid culture system and biologically relevant expression profiles of ACE2 and TMPRSS2 make nasal organoids present a correlate of in vivo protection of neutralizing mAbs exclusively. The organoid-based neutralization assays, superior to conventional cell-line-based assays, can recapitulate and predict the real-world efficacy of mAbs.
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