SARS-CoV-2 tetrameric RBD protein blocks viral infection and induces potent neutralizing antibody response

被引:3
|
作者
Liu, Zheng [1 ]
Yang, Chenglu [1 ]
Zhang, Haokun [1 ]
Cao, Guojie [1 ]
Wang, Senzhen [1 ]
Yin, Siwen [1 ]
Wang, Yanming [1 ]
机构
[1] Henan Univ, Sch Life Sci, Lab Epigenet & Translat Med, Kaifeng, Henan, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2022年 / 13卷
关键词
SARS-CoV-2; hACE2; 2xS-RBD-mFc; Vaccine; viral infection; RECEPTOR-BINDING DOMAIN; CORONAVIRUS SPIKE PROTEIN; VACCINES; COVID-19; DESIGN;
D O I
10.3389/fimmu.2022.960094
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The pandemic of coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has posed serious threats to global health and economy and calls for the development of safe treatments and effective vaccines. The receptor-binding domain in the spike protein (S-RBD) of SARS-CoV-2 is responsible for its binding to angiotensin-converting enzyme 2 (ACE2) receptor. It contains multiple dominant neutralizing epitopes and serves as an important antigen for the development of COVID-19 vaccines. Here, we showed that dimeric S-RBD-Fc and tetrameric 2xS(RBD)-Fc fusion proteins bind ACE2 with different affinity and block SARS-CoV-2 pseudoviral infection. Immunization of mice with S-RBD-Fc fusion proteins elicited high titer of RBD-specific antibodies with robust neutralizing activity against pseudoviral infections. As such, our study indicates that the polymeric S-RBD-Fc fusion protein can serve as a treatment agent as well as a vaccine for fighting COVID-19.
引用
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页数:10
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