Lessons from hepatitis E vaccine design

被引:26
|
作者
Li, Shaowei [1 ,2 ]
Zhang, Jun [1 ,2 ]
Xai, Ningshao [1 ,2 ]
机构
[1] Xiamen Univ, Sch Life Sci, State Key Lab Mol Vaccinol & Mol Diagnost, Xiamen 361005, Peoples R China
[2] Xiamen Univ, Sch Publ Hlth, Natl Inst Diagnost & Vaccine Dev Infect Dis, Xiamen 361005, Peoples R China
关键词
VIRUS-LIKE PARTICLES; CAPSID PROTEIN; MONOCLONAL-ANTIBODIES; STRUCTURAL BASIS; ORF3; PROTEIN; NEUTRALIZATION; IDENTIFICATION; EXPRESSION; EPITOPES; IMMUNODOMINANT;
D O I
10.1016/j.coviro.2015.04.003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Acute hepatitis E is still a major public health issue, especially in developing countries, and hepatitis E virus (HEV) infection will likely only be preventable through prophylactic vaccines. In this review, we describe the lessons learnt from developing the first commercial hepatitis E vaccine (Hecolin), launched to market in China in 2012. The antigenicity and immunogenicity of VLP immunogens concomitant with the scalable Escherichia coli system and our large-scale clinical verification resulted in the success of our vaccine. The structures of the HEV capsid protein in complex with different antibodies provide important molecular insights into capsid assembly and antibody neutralization of the virus, providing a paradigm for B-cell epitope-based vaccine design.
引用
收藏
页码:130 / 136
页数:7
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