Antibody cocktail effective against variants of SARS-CoV-2

被引:18
作者
Liang, Kang-Hao [1 ,2 ]
Chiang, Pao-Yin [1 ]
Ko, Shih-Han [1 ]
Chou, Yu-Chi [1 ]
Lu, Ruei-Min [1 ]
Lin, Hsiu-Ting [2 ]
Chen, Wan-Yu [2 ]
Lin, Yi-Ling [1 ,3 ]
Tao, Mi-Hua [1 ,3 ]
Jan, Jia-Tsrong [4 ]
Wu, Han-Chung [1 ,2 ]
机构
[1] Acad Sinica, Biomed Translat Res Ctr BioTReC, Taipei 11529, Taiwan
[2] Acad Sinica, Inst Cellular & Organism Biol, 128 Acad Rd,Sect 2, Taipei 11529, Taiwan
[3] Acad Sinica, Inst Biomed Sci, Taipei 11529, Taiwan
[4] Acad Sinica, Genom Res Ctr, Taipei 11529, Taiwan
关键词
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2); Receptor-binding domain (RBD); Neutralizing antibody; Cocktail therapy; CORONAVIRUS;
D O I
10.1186/s12929-021-00777-9
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background Coronavirus disease 2019 (COVID-19) is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), an RNA virus with a high mutation rate. Importantly, several currently circulating SARS-CoV-2 variants are associated with loss of efficacy for both vaccines and neutralizing antibodies. Methods We analyzed the binding activity of six highly potent antibodies to the spike proteins of SARS-CoV-2 variants, assessed their neutralizing abilities with pseudovirus and authentic SARS-CoV-2 variants and evaluate efficacy of antibody cocktail in Delta SARS-CoV-2-infected hamster models as prophylactic and post-infection treatments. Results The tested RBD-chAbs, except RBD-chAb-25, maintained binding ability to spike proteins from SARS-CoV-2 variants. However, only RBD-chAb-45 and -51 retained neutralizing activities; RBD-chAb-1, -15, -25 and -28 exhibited diminished neutralization for all SARS-CoV-2 variants. Notably, several cocktails of our antibodies showed low IC50 values (3.35-27.06 ng/ml) against the SARS-CoV-2 variant pseudoviruses including United Kingdom variant B.1.1.7 (Alpha), South Africa variant B.1.351 (Beta), Brazil variant P1 (Gamma), California variant B.1.429 (Epsilon), New York variant B.1.526 (Iota), and India variants, B.1.617.1 (Kappa) and B.1.617.2 (Delta). RBD-chAb-45, and -51 showed PRNT50 values 4.93-37.54 ng/ml when used as single treatments or in combination with RBD-chAb-15 or -28, according to plaque assays with authentic Alpha, Gamma and Delta SARS-CoV-2 variants. Furthermore, the antibody cocktail of RBD-chAb-15 and -45 exhibited potent prophylactic and therapeutic effects in Delta SARS-CoV-2 variant-infected hamsters. Conclusions The cocktail of RBD-chAbs exhibited potent neutralizing activities against SARS-CoV-2 variants. These antibody cocktails are highly promising candidate tools for controlling new SARS-CoV-2 variants, including Delta.
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页数:12
相关论文
共 45 条
[1]   New SARS-CoV-2 Variants - Clinical, Public Health, and Vaccine Implications [J].
Abdool Karim, Salim S. ;
de Oliveira, Tulio .
NEW ENGLAND JOURNAL OF MEDICINE, 2021, 384 (19) :1866-1868
[2]  
Annavajhala MK, 2021, NATURE, V597, P703, DOI [10.1038/s41586-021-03908-2, 10.1101/2021.02.23.21252259]
[3]  
[Anonymous], 2015, ARTERIOSCL THROM VAS
[4]   Antibody cocktail to SARS-CoV-2 spike protein prevents rapid mutational escape seen with individual antibodies [J].
Baum, Alina ;
Fulton, Benjamin O. ;
Wloga, Elzbieta ;
Copin, Richard ;
Pascal, Kristen E. ;
Russo, Vincenzo ;
Giordano, Stephanie ;
Lanza, Kathryn ;
Negron, Nicole ;
Ni, Min ;
Wei, Yi ;
Atwal, Gurinder S. ;
Murphy, Andrew J. ;
Stahl, Neil ;
Yancopoulos, George D. ;
Kyratsous, Christos A. .
SCIENCE, 2020, 369 (6506) :1014-+
[5]   DELTA CORONAVIRUS VARIANT: SCIENTISTS BRACE FOR IMPACT [J].
Callaway, Ewen .
NATURE, 2021, 595 (7865) :17-18
[6]   Potent Neutralizing Antibodies against SARS-CoV-2 Identified by High-Throughput Single-Cell Sequencing of Convalescent Patients' B Cells [J].
Cao, Yunlong ;
Su, Bin ;
Guo, Xianghua ;
Sun, Wenjie ;
Deng, Yongqiang ;
Bao, Linlin ;
Zhu, Qinyu ;
Zhang, Xu ;
Zheng, Yinghui ;
Geng, Chenyang ;
Chai, Xiaoran ;
He, Runsheng ;
Li, Xiaofeng ;
Lv, Qi ;
Zhu, Hua ;
Deng, Wei ;
Xu, Yanfeng ;
Wang, Yanjun ;
Qiao, Luxin ;
Tan, Yafang ;
Song, Liyang ;
Wang, Guopeng ;
Du, Xiaoxia ;
Gao, Ning ;
Liu, Jiangning ;
Xiao, Junyu ;
Su, Xiao-dong ;
Du, Zongmin ;
Feng, Yingmei ;
Qin, Chuan ;
Qin, Chengfeng ;
Jin, Ronghua ;
Xie, X. Sunney .
CELL, 2020, 182 (01) :73-+
[7]  
Cathcart AL., 2021, bioRxiv, DOI [DOI 10.1101/2021.03.09.434607, 10.1101/2021.03.09.434607]
[8]   Structural basis for accommodation of emerging B.1.351 and B.1.1.7 variants by two potent SARS-CoV-2 neutralizing antibodies [J].
Cerutti, Gabriele ;
Rapp, Micah ;
Guo, Yicheng ;
Bahna, Fabiana ;
Bimela, Jude ;
Reddem, Eswar R. ;
Yu, Jian ;
Wang, Pengfei ;
Liu, Lihong ;
Huang, Yaoxing ;
Ho, David D. ;
Kwong, Peter D. ;
Sheng, Zizhang ;
Shapiro, Lawrence .
STRUCTURE, 2021, 29 (07) :655-+
[9]   Risk of mortality in patients infected with SARS-CoV-2 variant of concern 202012/1: matched cohort study [J].
Challen, Robert ;
Brooks-Pollock, Ellen ;
Read, Jonathan M. ;
Dyson, Louise ;
Tsaneva-Atanasova, Krasimira ;
Danon, Leon .
BMJ-BRITISH MEDICAL JOURNAL, 2021, 372
[10]   Detection of 2019 novel coronavirus (2019-nCoV) by real-time RT-PCR (Publication with Expression of Concern) [J].
Corman, Victor M. ;
Landt, Olfert ;
Kaiser, Marco ;
Molenkamp, Richard ;
Meijer, Adam ;
Chu, Daniel K. W. ;
Bleicker, Tobias ;
Bruenink, Sebastian ;
Schneider, Julia ;
Schmidt, Marie Luisa ;
Mulders, Daphne G. J. C. ;
Haagmans, Bart L. ;
van der Veer, Bas ;
van den Brink, Sharon ;
Wijsman, Lisa ;
Goderski, Gabriel ;
Romette, Jean-Louis ;
Ellis, Joanna ;
Zambon, Maria ;
Peiris, Malik ;
Goossens, Herman ;
Reusken, Chantal ;
Koopmans, Marion P. G. ;
Drosten, Christian .
EUROSURVEILLANCE, 2020, 25 (03) :23-30