| Literature DB >> 29102169 |
Bin Li1, Luping Du2, Zhengyu Yu3, Bing Sun3, Xiangwei Xu3, Baochao Fan3, Rongli Guo3, Wanzhe Yuan4, Kongwang He5.
Abstract
Porcine epidemic diarrhea (PED) causes 80-100% mortality in neonatal piglets, and its causative agent, the porcine epidemic diarrhea virus (PEDV), poses an important threat to the swine industry worldwide. In this study, we prepared biodegradable poly (d,l-lactide-co-glycolide) (PLGA) nanoparticle-entrapped PEDV killed vaccine antigens (KAg) (PLGA-KAg). Late-term pregnant sows were intranasally inoculated with PLGA-KAg, and the mortality resulting from challenge with highly virulent PEDV was investigated in their passively immunized suckling piglets. PEDV-specific IgG and IgA antibody titers were enhanced in pregnant sows immunized with PLGA-KAg relative to the titers in sows inoculated with KAg. Similar results were seen in the passively immunized suckling piglets of these sows. Improved lymphocyte proliferation responses and IFN-γ levels were induced in pregnant sows immunized with PLGA-KAg compared with those vaccinated with KAg or with Montanide™ ISA 201 VG emulsified killed PEDV vaccine (201-KAg). Importantly, there was less piglet mortality in the group vaccinated with PLGA-KAg than in the groups vaccinated with KAg or 201-KAg. These results demonstrate that PLGA-KAg is a promising candidate vaccine that can provide protective immunity against PEDV infection in suckling piglets.Entities:
Keywords: Killed vaccine; PLGA nanoparticle; Porcine epidemic diarrhea virus; Protective immunity
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Year: 2017 PMID: 29102169 DOI: 10.1016/j.vaccine.2017.10.054
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641