Poly (D,L-lactide-co-glycolide) nanoparticle-entrapped vaccine induces a protective immune response against porcine epidemic diarrhea virus infection in piglets
Poly (D,L-lactide-co-glycolide) nanoparticle-entrapped vaccine induces a protective immune response against porcine epidemic diarrhea virus infection in piglets
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聚(d,l-丙交酯-乙交酯)纳米颗粒包埋疫苗可诱导仔猪产生针对猪流行性腹泻病毒感染的保护性免疫反应。
DOI:
10.1016/j.vaccine.2017.10.054
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发表时间:
2017-12-15
期刊:
影响因子:
5.5
通讯作者:
He, Kongwang
中科院分区:
文献类型:
--
作者:
Li, Bin;Du, Luping;He, Kongwang
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-ICAg 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-gamma levels were induced in pregnant sows immunized with PLGA-KAg compared with those vaccinated with KAg or with Montanid (TM) 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. (C) 2017 Elsevier Ltd. All rights reserved.