Ultrapotent and broad neutralization of SARS-CoV-2 variants by modular, tetravalent, bi-paratopic antibodies

被引:7
|
作者
Miersch, Shane [1 ]
Sharma, Nitin [2 ]
Saberianfar, Reza [1 ]
Chen, Chao [1 ]
Caccuri, Francesca [3 ]
Zani, Alberto [3 ]
Caruso, Arnaldo [3 ]
Case, James Brett [4 ]
Diamond, Michael S. [4 ,5 ,6 ,7 ]
Amarasinghe, Gaya K. [2 ]
Novelli, Giuseppe [8 ,9 ,10 ]
Sidhu, Sachdev S. [1 ]
机构
[1] Univ Toronto, Donnelly Ctr, Toronto, ON, Canada
[2] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA
[3] Univ Brescia, Sch Med, Dept Mol & Translat Med, Sect Microbiol, I-25123 Brescia, Italy
[4] Washington Univ, Sch Med, Dept Med, St Louis, MO USA
[5] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA
[6] Washington Univ, Sch Med, Dept Mol Microbiol, St Louis, MO USA
[7] Washington Univ, Sch Med, Andrew M & Jane M Bursky Ctr Human Immunol & Immu, St Louis, MO USA
[8] Univ Roma Tor Vergata, Dept Biomed & Prevent, Via Montpellier 1, I-00133 Rome, Italy
[9] IRCCS Neuromed, Pozzilli, Isernia, Italy
[10] Univ Nevada, Sch Med, Dept Pharmacol, Reno, NV USA
来源
CELL REPORTS | 2022年 / 39卷 / 09期
基金
加拿大创新基金会; 美国国家卫生研究院;
关键词
REPLICATION; DIVERSITY; ACE2;
D O I
10.1016/j.celrep.2022.110905
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Neutralizing antibodies (nAbs) that target the SARS-CoV-2 spike protein have received emergency use approval for treatment of COVID-19. However, with the emergence of variants of concern, there is a need for new treatment options. We report a format that enables modular assembly of bi-paratopic tetravalent nAbs with antigen-binding sites from two distinct nAbs. The tetravalent nAb purifies in high yield and exhibits biophysical characteristics that are comparable to those of clinically used therapeutic antibodies. The tetravalent nAb binds to the spike protein trimer at least 100-fold more tightly than bivalent IgGs (apparent K-D < 1 pM) and neutralizes a broad array of SARS-CoV-2 pseudoviruses, chimeric viruses, and authentic viral variants with high potency. Together, these results establish the tetravalent diabody-Fc-Fab as a robust, modular platform for rapid production of drug-grade nAbs with potencies and breadth of coverage that greatly exceed those of conventional bivalent IgGs.
引用
收藏
页数:15
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