Biodegradable Nanoparticle-Entrapped Vaccine Induces Cross-Protective Immune Response against a Virulent Heterologous Respiratory Viral Infection in Pigs

被引:30
作者
Dwivedi, Varun [1 ,2 ]
Manickam, Cordelia [1 ,2 ]
Binjawadagi, Basavaraj [1 ,2 ]
Joyappa, Dechamma [3 ]
Renukaradhya, Gourapura J. [1 ,2 ]
机构
[1] Ohio State Univ, Ohio Agr Res & Dev Ctr, Food Anim Hlth Res Program, Wooster, OH 44691 USA
[2] Ohio State Univ, Dept Vet Prevent Med, Columbus, OH 43210 USA
[3] Indian Vet Res Inst, Foot & Mouth Dis Lab, Hebbal, Bengaluru, India
基金
美国农业部;
关键词
DENDRITIC CELL MATURATION; SYNDROME VIRUS-VACCINE; INTRANASAL DELIVERY; PORCINE; MICROSPHERES; ANTIGEN; SYSTEM; MICE; IMMUNIZATION; ANTIBODY;
D O I
10.1371/journal.pone.0051794
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Biodegradable nanoparticle-based vaccine development research is unexplored in large animals and humans. In this study, we illustrated the efficacy of nanoparticle-entrapped UV-killed virus vaccine against an economically important respiratory viral disease of pigs called porcine reproductive and respiratory syndrome virus (PRRSV). We entrapped PLGA [poly (lactide-co-glycolides)] nanoparticles with killed PRRSV antigens (Nano-KAg) and detected its phagocytosis by pig alveolar macrophages. Single doses of Nano-KAg vaccine administered intranasally to pigs upregulated innate and PRRSV specific adaptive responses. In a virulent heterologous PRRSV challenge study, Nano-KAg vaccine significantly reduced the lung pathology and viremia, and the viral load in the lungs. Immunologically, enhanced innate and adaptive immune cell population and associated cytokines with decreased secretion of immunosuppressive mediators were observed at both mucosal sites and blood. In summary, we demonstrated the benefits of intranasal delivery of nanoparticle-based viral vaccine in eliciting cross-protective immune response in pigs, a potential large animal model.
引用
收藏
页数:11
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