Enterovirus D68 virus-like particles expressed in Pichia pastoris potently induce neutralizing antibody responses and confer protection against lethal viral infection in mice

被引:32
|
作者
Zhang, Chao [1 ,2 ]
Zhang, Xueyang [2 ]
Zhang, Wei [2 ]
Dai, Wenlong [2 ]
Xie, Jing [1 ]
Ye, Liping [1 ]
Wang, Hongli [1 ]
Chen, Huan [1 ]
Liu, Qingwei [2 ]
Gong, Sitang [1 ]
Geng, Lanlan [1 ]
Huang, Zhong [1 ,2 ]
机构
[1] Guangzhou Med Univ, Guangzhou Inst Pediat, Guangzhou Women & Childrens Med Ctr, Joint Ctr Infect & Immun,Dept Gastroenterol, Guangzhou 510623, Guangdong, Peoples R China
[2] Chinese Acad Sci, Inst Pasteur Shanghai, Unit Vaccinol & Antiviral Strategies, CAS Key Lab Mol Virol & Immunol, Shanghai 200031, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
ACUTE FLACCID MYELITIS; COXSACKIEVIRUS A16; MONOCLONAL-ANTIBODIES; IMMUNE-RESPONSES; LINEAR EPITOPES; VACCINE; CHALLENGE; CHILDREN; IDENTIFICATION; IMMUNIZATION;
D O I
10.1038/s41426-017-0005-x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Enterovirus D68 (EV-D68) has been increasingly associated with severe respiratory illness and neurological complications in children worldwide. However, no vaccine is currently available to prevent EV-D68 infection. In the present study, we investigated the possibility of developing a virus-like particle (VLP)-based EV-D68 vaccine. We found that co-expression of the P1 precursor and 3CD protease of EV-D68 in Pichia pastoris yeast resulted in the generation of EV-D68 VLPs, which were composed of processed VP0, VP1, and VP3 capsid proteins and were visualized as similar to 30 nm spherical particles. Mice immunized with these VLPs produced serum antibodies capable of specifically neutralizing EV-D68 infections in vitro. The in vivo protective efficacy of the EV-D68 VLP candidate vaccine was assessed in two challenge experiments. The first challenge experiment showed that neonatal mice born to the VLP-immunized dams were fully protected from lethal EV-D68 infection, whereas in the second experiment, passive transfer of anti-VLP sera was found to confer complete protection in the recipient mice. Collectively, these results demonstrate the proof-of-concept for VLP-based broadly effective EV-D68 vaccines.
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页数:9
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