Ferritin Nanoparticle Delivery of the E2 Protein of Classical Swine Fever Virus Completely Protects Pigs from Lethal Challenge

被引:2
|
作者
Zhong, Dailang [1 ]
Lu, Zhanhao [1 ]
Xia, Yu [1 ,2 ]
Wu, Hongxia [1 ]
Zhang, Xinyu [1 ,3 ]
Li, Mingzhi [1 ,2 ]
Song, Xin [1 ]
Wang, Yanjin [1 ]
Moon, Assad [1 ]
Qiu, Hua-Ji [1 ]
Li, Yongfeng [1 ]
Sun, Yuan [1 ,2 ]
机构
[1] Chinese Acad Agr Sci, Harbin Vet Res Inst, State Key Lab Anim Dis Control & Prevent, Harbin 150069, Peoples R China
[2] Henan Inst Sci & Technol, Sch Anim Sci & Technol, Xinxiang 453003, Peoples R China
[3] Foshan Univ, Sch Life Sci & Engn, Foshan 528225, Peoples R China
关键词
classical swine fever virus; E2; protein; ferritin; self-assembled nanoparticles; cell-mediated immune responses; neutralizing antibodies; VACCINES;
D O I
10.3390/vaccines12060629
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Classical swine fever (CSF), caused by the classical swine fever virus (CSFV), results in significant economic losses to the swine industry in many countries. Vaccination represents the primary strategy to control CSF and the CSFV E2 protein is known as the major protective antigen. However, the E2 protein expressed or presented by different systems elicits distinct immune responses. In this study, we established a stable CHO cell line to express the E2 protein and delivered it using self-assembled ferritin nanoparticles (NPs). Subsequently, we compared the adaptive immune responses induced by the E2-ferritin NPs and the monomeric E2 protein produced by the CHO cells or a baculovirus expression system. The results revealed that the NP-delivered E2 protein elicited higher titers of neutralizing antibodies than did the monomeric E2 protein in pigs. Importantly, only the NP-delivered E2 protein significantly induced CSFV-specific IFN-gamma-secreting cells. Furthermore, all the pigs inoculated with the E2-ferritin NPs were completely protected from a lethal CSFV challenge infection. These findings demonstrate the ability of the E2-ferritin NPs to protect pigs against the lethal CSFV challenge by eliciting robust humoral and cellular immune responses.
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页数:18
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