伪狂犬病
病毒学
病毒
生物
免疫系统
佐剂
免疫
疱疹病毒科
微生物学
疱疹病毒科
免疫学
病毒性疾病
作者
Xujiao Ren,Nan Cao,Linxing Tian,Wenqiang Liu,Hechao Zhu,Zhenxiang Rong,Manman Yao,Xiangmin Li,Ping Qian
标识
DOI:10.1016/j.vetmic.2023.109799
摘要
Pseudorabies virus (PRV) mainly causes pseudorabies (PR) or Aujeszky's disease in pigs and can infect humans, raising public health concerns about zoonotic and interspecies transmission of PR. With the emergence of PRV variants in 2011, the classic attenuated PRV vaccine strains have failed to protect many swine herds against PR. Herein, we developed a self-assembled nanoparticle vaccine that induces potent protective immunity against PRV infection. PRV glycoprotein D (gD) was expressed using the baculovirus expression system and further presented on the lumazine synthase (LS) 60-meric protein scaffolds via the SpyTag003/SpyCatcher003 covalent coupling system. In mouse and piglet models, LSgD nanoparticles emulsified with the ISA 201VG adjuvant elicited robust humoral and cellular immune responses. Furthermore, LSgD nanoparticles provided effective protection against PRV infection and eliminated pathological symptoms in the brain and lungs. Collectively, the gD-based nanoparticle vaccine design appears to be a promising candidate for potent protection against PRV infection.
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