Self-Assembling Nanovaccine Fused with Flagellin Enhances Protective Effect against Foot-and-Mouth Disease Virus

被引:3
|
作者
Pei, Chenchen [1 ,2 ]
Dong, Hu [1 ,2 ]
Teng, Zhidong [1 ,2 ]
Wei, Sumin [1 ,2 ]
Zhang, Yun [1 ,2 ]
Yin, Shuanghui [1 ,2 ]
Tang, Jianli [1 ,2 ]
Sun, Shiqi [1 ,2 ]
Guo, Huichen [1 ,2 ,3 ]
机构
[1] Lanzhou Univ, Chinese Acad Agr Sci, Lanzhou Vet Res Inst, Coll Vet Med,State Key Lab Anim Dis Control & Prev, Lanzhou 730046, Peoples R China
[2] Gansu Prov Res Ctr Basic Disciplines Pathogen Biol, Lanzhou 730046, Peoples R China
[3] Yangtze Univ, Coll Anim Sci, Jingzhou 434023, Peoples R China
基金
国家重点研发计划;
关键词
foot-and-mouth disease; flagellin; self-assembling; nanoparticles; nanovaccine; IMMUNE-RESPONSE; DIVA VACCINE; INFECTION; NANOPARTICLES; INDUCTION; PARTICLES; EPITOPE;
D O I
10.3390/vaccines11111675
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Nanovaccines based on self-assembling nanoparticles (NPs) can show conformational epitopes of antigens and they have high immunogenicity. In addition, flagellin, as a biological immune enhancer, can be fused with an antigen to considerably enhance the immune effect of antigens. In improving the immunogenicity and stability of a foot-and-mouth disease virus (FMDV) antigen, novel FMDV NP antigens were prepared by covalently coupling the VP1 protein and truncated flagellin containing only N-terminus D0 and D1 (N-terminal aa 1-99, nFLiC) with self-assembling NPs (i301). The results showed that the fusion proteins VP1-i301 and VP1-i301-nFLiC can assemble into NPs with high thermal tolerance and stability, obtain high cell uptake efficiency, and upregulate marker molecules and immune-stimulating cytokines in vitro. In addition, compared with monomeric VP1 antigen, high-level cytokines were stimulated with VP1-i301 and VP1-i301-nFLiC nanovaccines in guinea pigs, to provide clinical protection against viral infection comparable to an inactivated vaccine. This study provides new insight for the development of a novel FMD vaccine.
引用
收藏
页数:16
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