戊型肝炎病毒
病毒学
衣壳
病毒
重组DNA
类病毒颗粒
生物
免疫系统
基因型
免疫学
基因
遗传学
作者
Rushi Liu,Chufan Tan,Junwen Wu,Xu Ye,Xiaofeng Li,Zhihong Zhong,Sang Li,Yilan Qiu,Bo Feng
出处
期刊:Heliyon
[Elsevier]
日期:2023-04-01
卷期号:9 (4): e15284-e15284
标识
DOI:10.1016/j.heliyon.2023.e15284
摘要
HEV (Hepatitis E virus) is an infectious disease transmitted between humans and animals, which poses a severe threat to the biological safety and property throughout the world. The disease is especially severe in patients with potential liver cirrhosis and women during pregnancy. There is no specific and thorough HEV treatment at present. The development of hepatitis E virus vaccine is vital to the prevention of viral hepatitis worldwide. Since HEV cannot grow adequately in vitro, vaccine developed by devitalized virus particles does not work. Exploration of HEV-like structures is essential for the development of functional vaccines against HEV infection. ORF2 encodes the structural proteins of HEV, some of which can automatically assemble into virus-like particles (VLP) in this experiment, the recombinant capsid protein p27 was expressed in E. coli and the VLP formed by p27 was used to immunize mice. The results showed that the VLP formed by recombinant P27 had similar particle size to that of HEV; the immune dose produced by p27 was positively correlated with the immune effect. Compared with other genetic engineering subunit vaccines, P27 protein has a better application prospect.
科研通智能强力驱动
Strongly Powered by AbleSci AI