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Microencapsulated enterotoxigenic Escherichia coli and detached fimbriaefor peroral vaccination of pigs

机译:微囊化产肠毒素大肠杆菌和分离菌毛用于猪的经口疫苗接种

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The feasibility of peroral immunisation with microencapsulated Escherichia coli and detached fimbriae to prevent enterotoxigenic E. coli infections in pigs was examined. For this E. coli and fimbriae were microencapsulated into poly(lactide-co-glycolide) microspheres by spray-drying. Various microsphere formulations designed to deliver priming and booster doses were fed to new-born and weaned pigs. The pigs were challenged 19 days after the booster dose by peroral administration of an infective dose of the homologous E. coli. Serum IgA antibody titres and excretion of challenge E. coli, as indicators fur colonisation, were determined. The data showed that no significant serum antibodies were induced, and E. coli colonisation was not reduced by the peroral administration of the various antigen-loaded microspheres. These results are in contradiction to some of the previously published experiments typically in rats or rabbits, where model antigens or unpractical immunisation procedures have frequently been used.
机译:检查了用微囊化大肠杆菌和分离的菌毛进行口服免疫以预防猪中肠毒素性大肠杆菌感染的可行性。为此,通过喷雾干燥将大肠杆菌和菌毛微囊化到聚(丙交酯-共-乙交酯)微球中。将设计用于提供初免和加强剂量的各种微球制剂喂给新生和断奶的猪。通过口服给予感染剂量的同源大肠杆菌,在加强剂量后19天对猪进行攻击。确定血清IgA抗体滴度和挑战大肠杆菌的排泄,作为定殖的指标。数据显示未诱导出明显的血清抗体,并且经口服施用各种载有抗原的微球体也未减少大肠杆菌的定殖。这些结果与通常在大鼠或兔子中进行的某些先前发表的实验相矛盾,在老鼠或兔子中,经常使用模型抗原或不实用的免疫程序。

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