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Humoral immune response to authentic circulating severe acute respiratory syndrome coronavirus 2 variants elicited by booster vaccination with distinct receptor-binding domain subunits in mice
被引:2
|作者:
Jiang, Yushan
[1
]
Zhang, Huan
[2
]
Yu, Jianhai
[1
]
Huang, Dong
[1
]
Zhai, Linlin
[1
]
Li, Mengjun
[1
]
Wang, Yuelin
[1
]
Ren, Zuning
[1
]
Zou, Lirong
[2
]
Zheng, Zhonghua
[2
]
Hu, Huanyu
[1
]
Zhang, Junfang
[3
]
Zhang, Bao
[1
]
Zhao, Wei
[1
]
Yang, Xingfen
[1
]
Li, Baisheng
[2
]
Shen, Chenguang
[1
]
机构:
[1] Southern Med Univ, Sch Publ Hlth, Guangdong Prov Key Lab Trop Dis Res, BSL 3 Lab Guangdong, Guangzhou, Peoples R China
[2] Prov Ctr Dis Control & Prevent, Guangzhou, Peoples R China
[3] Shenzhen Immuthy Biotech Co Ltd, Shenzhen, Peoples R China
基金:
中国国家自然科学基金;
关键词:
booster vaccination;
humoral immune response;
SARS-CoV-2;
D O I:
10.1002/jmv.27882
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants could induce immune escape by mutations of the spike protein which are threatening to weaken vaccine efficacy. A booster vaccination is expected to increase the humoral immune response against SARS-CoV-2 variants in the population. We showed that immunization with two doses of wild type receptor-binding domain (RBD) protein, and booster vaccination with wild type or variant RBD protein all significantly increased binding and neutralizing antibody titers against wild type SARS-CoV-2 and its variants in mice. Only the booster immunization by Omicron (BA.1)RBD induced a strong antibody titer against the omicron virus strain and comparable antibody titers against all the other virus strains. These findings might shed the light on coronavirus disease 2019 booster immunogens.
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页码:4533 / 4538
页数:6
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