TY - JOUR
T1 - Organoid-based neutralization assays reveal a distinctive profile of SARS-CoV-2 antibodies and recapitulate the real-world efficacy
AU - Wan, Zhixin
AU - Li, Cun
AU - Zhou, Ying
AU - Yu, Yifei
AU - Chiu, Man Chun
AU - Huang, Jingjing
AU - Zhang, Shuxin
AU - Zhu, Xiaoxin
AU - Lan, Qiaoshuai
AU - Deng, Yanlin
AU - Xue, Wei
AU - Jiang, Chengfan
AU - Wu, Jiali
AU - Zhao, Zijun
AU - Cai, Jian-Piao
AU - Huang, Lin
AU - Zhang, Yong
AU - Liu, Xiaojuan
AU - Zhang, Zheng
AU - Chu, Hin
AU - Zhang, Linqi
AU - Chen, Zhiwei
AU - To, Kelvin Kai-Wang
AU - Yuen, Kwok-Yung
AU - Clevers, Hans
AU - Zhou, Jie
N1 - Publisher Copyright:
Copyright © 2025 the Author(s).
PY - 2025/9/2
Y1 - 2025/9/2
N2 - 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.
AB - 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.
KW - Angiotensin-Converting Enzyme 2/metabolism
KW - Animals
KW - Antibodies, Monoclonal/immunology
KW - Antibodies, Neutralizing/immunology
KW - Antibodies, Viral/immunology
KW - COVID-19/immunology
KW - Humans
KW - Mice
KW - Neutralization Tests/methods
KW - Organoids/immunology
KW - SARS-CoV-2/immunology
KW - Serine Endopeptidases/metabolism
KW - Spike Glycoprotein, Coronavirus/immunology
U2 - 10.1073/pnas.2509616122
DO - 10.1073/pnas.2509616122
M3 - Article
C2 - 40875807
SN - 0027-8424
VL - 122
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 35
M1 - e2509616122
ER -