Worrall E E, Priadi A
TyMawr, Trefilan, Lampeter, Ceredigion SA48 8RD, United Kingdom.
Vaccine. 2009 Jun 24;27(31):4161-8. doi: 10.1016/j.vaccine.2009.04.058. Epub 2009 May 9.
A simple, effective inactivated avian flu vaccine composed of three homologous highly pathogenic (HP) H5N1 strains combined with Clostridium perfringens type A 107 sialidase/neuramindase and chitosan as a trans epithelial carrier adjuvant applied intranasally to poultry is described. Poultry were vaccinated with an inactivated, solvent split, chitosan adjuvanted intranasal (IN) vaccine with and without C. perfringens sialidase and the resulting serum IgG antibody measured by haemagglutination inhibition (HI) and mucosal IgA by ELISA. The clinical effectiveness was demonstrated by disease intervention field trials, where the ability of an intranasal vaccine containing three homologous inactivated solvent split HP H5N1 strains, C. perfringens sialidase and chitosan was successful in controlling the disease in intensively reared commercial chickens. Evidence is presented by demonstrating effective intervention with IN vaccine during outbreaks in poultry previously vaccinated with commercial heterologous H5N2 intramuscular (IM) vaccine and reassorted H5N1 Re-1 vaccine which had failed to protect intensively reared birds. Intervention with the IN vaccine in such flocks completely halted the infection within 2-5 days. Survivors ceased to excrete live virus. Stimulation of the common mucosal immune system (CMIS) and the early production of secretory IgA and subsequently humoral IgG demonstrated by laboratory controlled experiments and field studies revealed the ability of intranasally vaccinated birds to resist lethal virus challenge. A strategy of mucosal immunisation is recommended to reduce the incidence of disease in intensively reared poultry and thus minimise the generation and transfer of mutated highly pathogenic subtypes to humans and other animals.
描述了一种简单、有效的灭活禽流感疫苗,该疫苗由三种同源高致病性(HP)H5N1毒株与A型产气荚膜梭菌107唾液酸酶/神经氨酸酶以及壳聚糖作为经上皮载体佐剂组成,通过鼻内给药用于家禽。给家禽接种含或不含产气荚膜梭菌唾液酸酶的灭活、溶剂裂解、壳聚糖佐剂鼻内(IN)疫苗,并通过血凝抑制(HI)测定产生的血清IgG抗体,通过ELISA测定黏膜IgA。通过疾病干预现场试验证明了临床有效性,其中含有三种同源灭活溶剂裂解HP H5N1毒株、产气荚膜梭菌唾液酸酶和壳聚糖的鼻内疫苗成功控制了密集饲养的商业鸡群中的疾病。通过在先前接种商业异源H5N2肌肉注射(IM)疫苗和重配H5N1 Re-1疫苗但未能保护密集饲养禽类的家禽爆发期间用IN疫苗进行有效干预来提供证据。在此类鸡群中用IN疫苗进行干预在2至5天内完全阻止了感染。存活鸡不再排泄活病毒。实验室对照实验和现场研究表明,鼻内接种的禽类刺激共同黏膜免疫系统(CMIS)以及早期产生分泌性IgA并随后产生体液IgG,显示出其抵抗致死性病毒攻击的能力。建议采用黏膜免疫策略来降低密集饲养家禽的疾病发生率,从而最大限度地减少高致病性变异亚型向人类和其他动物的产生和传播。