Three epitope-distinct human antibodies from RenMab mice neutralize SARS-CoV-2 and cooperatively minimize the escape of mutants

被引:13
|
作者
Nie, Jianhui [1 ,2 ]
Xie, Jingshu [3 ]
Liu, Shuo [1 ,2 ]
Wu, Jiajing [1 ,2 ]
Liu, Chuan [4 ]
Li, Jianhui [3 ]
Liu, Yacui [3 ]
Wang, Meiyu [1 ,2 ]
Zhao, Huizhen [3 ]
Zhang, Yabo [3 ]
Yao, Jiawei [3 ]
Chen, Lei [3 ]
Shen, Yuelei [3 ]
Yang, Yi [3 ]
Wang, Hong-Wei [5 ]
Wang, Youchun [1 ,2 ]
Huang, Weijin [1 ,2 ]
机构
[1] Natl Inst Food & Drug Control NIFDC, Div HIV AIDS & Sextransmitted Virus Vaccines, Inst Biol Product Control, Beijing, Peoples R China
[2] WHO Collaborating Ctr Stand & Evaluat Biol, Beijing, Peoples R China
[3] Beijing Biocytogen Co Ltd, Beijing, Peoples R China
[4] Shuimu BioSci Co Ltd, Beijing, Peoples R China
[5] Tsinghua Univ, Minist Educ, Key Lab Prot Sci,Sch Life Sci, Tsinghua Peking Joint Ctr Life Sci,Beijing Adv In, Beijing, Peoples R China
基金
比尔及梅琳达.盖茨基金会; 中国国家自然科学基金;
关键词
MUTATIONS; SPIKE;
D O I
10.1038/s41421-021-00292-z
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Coronavirus disease 2019 (COVID-19), a pandemic disease caused by the newly emerging severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has caused more than 3.8 million deaths to date. Neutralizing antibodies are effective therapeutic measures. However, many naturally occurring mutations at the receptor-binding domain (RBD) have emerged, and some of them can evade existing neutralizing antibodies. Here, we utilized RenMab, a novel mouse carrying the entire human antibody variable region, for neutralizing antibody discovery. We obtained several potent RBD-blocking antibodies and categorized them into four distinct groups by epitope mapping. We determined the involved residues of the epitope of three representative antibodies by cryo-electron microscopy (Cryo-EM) studies. Moreover, we performed neutralizing experiments with 50 variant strains with single or combined mutations and found that the mixing of three epitope-distinct antibodies almost eliminated the mutant escape. Our study provides a sound basis for the rational design of fully human antibody cocktails against SARS-CoV-2 and pre-emergent coronaviral threats.
引用
收藏
页数:11
相关论文
共 50 条
  • [1] Three epitope-distinct human antibodies from RenMab mice neutralize SARS-CoV-2 and cooperatively minimize the escape of mutants
    Jianhui Nie
    Jingshu Xie
    Shuo Liu
    Jiajing Wu
    Chuan Liu
    Jianhui Li
    Yacui Liu
    Meiyu Wang
    Huizhen Zhao
    Yabo Zhang
    Jiawei Yao
    Lei Chen
    Yuelei Shen
    Yi Yang
    Hong-Wei Wang
    Youchun Wang
    Weijin Huang
    Cell Discovery, 7
  • [2] Human antibodies can neutralize SARS-CoV-2
    Catalan-Dibene J.
    Nature Reviews Immunology, 2020, 20 (6) : 350 - 350
  • [3] Nanobodies from camelid mice and llamas neutralize SARS-CoV-2 variants
    Jianliang Xu
    Kai Xu
    Seolkyoung Jung
    Andrea Conte
    Jenna Lieberman
    Frauke Muecksch
    Julio Cesar Cetrulo Lorenzi
    Solji Park
    Fabian Schmidt
    Zijun Wang
    Yaoxing Huang
    Yang Luo
    Manoj S. Nair
    Pengfei Wang
    Jonathan E. Schulz
    Lino Tessarollo
    Tatsiana Bylund
    Gwo-Yu Chuang
    Adam S. Olia
    Tyler Stephens
    I-Ting Teng
    Yaroslav Tsybovsky
    Tongqing Zhou
    Vincent Munster
    David D. Ho
    Theodora Hatziioannou
    Paul D. Bieniasz
    Michel C. Nussenzweig
    Peter D. Kwong
    Rafael Casellas
    Nature, 2021, 595 : 278 - 282
  • [4] Nanobodies from camelid mice and llamas neutralize SARS-CoV-2 variants
    Xu, Jianliang
    Xu, Kai
    Jung, Seolkyoung
    Conte, Andrea
    Lieberman, Jenna
    Muecksch, Frauke
    Lorenzi, Julio Cesar Cetrulo
    Park, Solji
    Schmidt, Fabian
    Wang, Zijun
    Huang, Yaoxing
    Luo, Yang
    Nair, Manoj S.
    Wang, Pengfei
    Schulz, Jonathan E.
    Tessarollo, Lino
    Bylund, Tatsiana
    Chuang, Gwo-Yu
    Olia, Adam S.
    Stephens, Tyler
    Teng, I-Ting
    Tsybovsky, Yaroslav
    Zhou, Tongqing
    Munster, Vincent
    Ho, David D.
    Hatziioannou, Theodora
    Bieniasz, Paul D.
    Nussenzweig, Michel C.
    Kwong, Peter D.
    Casellas, Rafael
    NATURE, 2021, 595 (7866) : 278 - +
  • [5] Characterization of SARS-CoV-2 Escape Mutants to a Pair of Neutralizing Antibodies Targeting the RBD and the NTD
    Peter, Antonia Sophia
    Gruener, Eva
    Socher, Eileen
    Fraedrich, Kirsten
    Richel, Elie
    Mueller-Schmucker, Sandra
    Cordsmeier, Arne
    Ensser, Armin
    Sticht, Heinrich
    Ueberla, Klaus
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (15)
  • [6] SARS-CoV-2 Spike Protein Mutations and Escape from Antibodies: A Computational Model of Epitope Loss in Variants of Concern
    Triveri, Alice
    Serapian, Stefano A.
    Marchetti, Filippo
    Doria, Filippo
    Pavoni, Silvia
    Cinquini, Fabrizio
    Moroni, Elisabetta
    Rasola, Andrea
    Frigerio, Francesco
    Colombo, Giorgio
    JOURNAL OF CHEMICAL INFORMATION AND MODELING, 2021, 61 (09) : 4687 - 4700
  • [7] Bispecific antibodies targeting distinct regions of the spike protein potently neutralize SARS-CoV-2 variants of concern
    Cho, Hyeseon
    Gonzales-Wartz, Kristina Kay
    Huang, Deli
    Yuan, Meng
    Peterson, Mary
    Liang, Janie
    Beutler, Nathan
    Torres, Jonathan L.
    Cong, Yu
    Postnikova, Elena
    Bangaru, Sandhya
    Talana, Chloe Adrienna
    Shi, Wei
    Yang, Eun Sung
    Zhang, Yi
    Leung, Kwanyee
    Wang, Lingshu
    Peng, Linghang
    Skinner, Jeff
    Li, Shanping
    Wu, Nicholas C.
    Liu, Hejun
    Dacon, Cherrelle
    Moyer, Thomas
    Cohen, Melanie
    Zhao, Ming
    Lee, Frances Eun-Hyung
    Weinberg, Rona S.
    Douagi, Iyadh
    Gross, Robin
    Schmaljohn, Connie
    Pegu, Amarendra
    Mascola, John R.
    Holbrook, Michael
    Nemazee, David
    Rogers, Thomas F.
    Ward, Andrew B.
    Wilson, Ian A.
    Crompton, Peter D.
    Tan, Joshua
    SCIENCE TRANSLATIONAL MEDICINE, 2021, 13 (616)
  • [8] Escape from neutralizing antibodies by SARS-CoV-2 spike protein variants
    Weisblum, Yiska
    Schmidt, Fabian
    Zhang, Fengwen
    DaSilva, Justin
    Poston, Daniel
    Lorenzi, Julio C. C.
    Muecksch, Frauke
    Rutkowska, Magdalena
    Hoffmann, Hans-Heinrich
    Michailidis, Eleftherios
    Gaebler, Christian
    Agudelo, Marianna
    Cho, Alice
    Wang, Zijun
    Gazumyan, Anna
    Cipolla, Melissa
    Luchsinger, Larry
    Hillyer, Christopher D.
    Caskey, Marina
    Robbiani, Davide F.
    Rice, Charles M.
    Nussenzweig, Michel C.
    Hatziioannou, Theodora
    Bieniasz, Paul D.
    ELIFE, 2020, 9 : 1
  • [9] Human monoclonal antibodies to the spike subdomain 1 neutralize SARS-CoV-2 and its variants of concern
    Bianchini, F.
    Crivelli, V.
    Abernathy, M. E.
    Guerra, C.
    Palus, M.
    Marcotte, H.
    Piralla, A.
    Pedotti, M.
    De Gasparo, R.
    Simonelli, L.
    Matkovic, M.
    Toscano, C.
    Biggiogero, M.
    Calvaruso, V.
    Rincon, T. Cervantes
    Muri, J.
    Podesvova, L.
    Shanbhag, A.
    Celoria, A.
    Sgrignani, J.
    Stefanik, M.
    Honig, V.
    Pranclova, V.
    Michalcikova, T.
    Prochazka, J.
    Guerrini, G.
    Mehn, D.
    Ciabattini, A.
    Abolhassani, H.
    Jarrossay, D.
    Uguccioni, M.
    Medaglini, D.
    Pan-Hammarstrom, Q.
    Calzolai, L.
    Baldanti, F.
    Franzetti-Pellanda, A.
    Garzoni, C.
    Sedlacek, R.
    Ruzek, D.
    Varani, L.
    Cavalli, A.
    Barnes, C. O.
    Robbiani, D. F.
    SWISS MEDICAL WEEKLY, 2022, 152 : 10S - 10S
  • [10] Characterization of SARS-CoV-2 Spike mutations important for infection of mice and escape from human immune sera
    Raveen Rathnasinghe
    Sonia Jangra
    Chengjin Ye
    Anastasija Cupic
    Gagandeep Singh
    Carles Martínez-Romero
    Lubbertus C. F. Mulder
    Thomas Kehrer
    Soner Yildiz
    Angela Choi
    Stephen T. Yeung
    Ignacio Mena
    Virginia Gillespie
    Jana De Vrieze
    Sadaf Aslam
    Daniel Stadlbauer
    David A. Meekins
    Chester D. McDowell
    Velmurugan Balaraman
    Michael J. Corley
    Juergen A. Richt
    Bruno G. De Geest
    Lisa Miorin
    Florian Krammer
    Luis Martinez-Sobrido
    Viviana Simon
    Adolfo García-Sastre
    Michael Schotsaert
    Nature Communications, 13