LeJambre L F, Windon R G, Smith W D
CSIRO Livestock Industries, F.D. McMaster Laboratory, Private Mail Bag, Armidale, NSW 2350,
Vet Parasitol. 2008 May 31;153(3-4):302-12. doi: 10.1016/j.vetpar.2008.01.032. Epub 2008 Feb 3.
In a replicated trial, parasitological and antibody responses of grazing weaner Merino sheep were assessed following vaccination with gut membrane proteins prepared from adult worms of the gastrointestinal nematode, Haemonchus contortus. Each vaccinated animal received 100 microg native H11 and 100 microg native H-gal-GP combined together in 5mg Quil A administered intramuscularly on days 0, 34, 80 and 127. Control animals received 5mg Quil A alone on the same days. Vaccinated and unvaccinated control animals grazed pastures contaminated with the parasite from day 34 of the trial, and levels of parasitism were monitored by worm-egg counts (WECs) in faeces and packed cell volumes (PCVs) in blood. The level of larval contamination on pasture was estimated from the worm counts of tracer sheep introduced monthly to the paddocks. WECs and anaemia were significantly reduced in vaccinated animals, and, in contrast to vaccinates, all control sheep required salvage treatment with anthelmintic. By the last 2 months of the trial, pastures grazed by vaccinated animals had significantly lower contamination with H. contortus larvae. Vaccinated animals had high levels of vaccine antigen-specific IgG1 and IgG2 antibodies in plasma, whereas those responses in the control sheep were very low. IgG1 titres in the vaccinated group, but not IgG2 titres, were inversely correlated with worm-egg counts. The levels of systemic IgA and IgE remained low but increased in both groups towards the end of the experiment most probably from exposure to the natural infection from pasture. The results showed that H11 and H-gal-GP behaved like "hidden" antigens producing high levels of protection that were probably mediated through mechanisms involving antibodies, and in particular, IgG1. It was concluded that if similar protective effects could be obtained with recombinant versions of the proteins present in either H11 or H-gal-GP, then the prospects for a commercial Haemonchus vaccine were real.
在一项重复试验中,对接种了由胃肠道线虫捻转血矛线虫成虫制备的肠膜蛋白的放牧断奶美利奴羊的寄生虫学和抗体反应进行了评估。每只接种动物在第0、34、80和127天接受100微克天然H11和100微克天然H-gal-GP混合于5毫克 Quil A中,通过肌肉注射给药。对照动物在同一天单独接受5毫克 Quil A。从试验第34天起,接种和未接种的对照动物在感染寄生虫的牧场上放牧,通过粪便中的虫卵计数(WECs)和血液中的红细胞压积(PCVs)监测寄生虫感染水平。根据每月引入围场的示踪羊的蠕虫计数估算牧场上幼虫污染水平。接种动物的WECs和贫血症显著降低,与接种动物形成对比的是,所有对照羊都需要用驱虫药进行挽救治疗。到试验最后两个月,接种动物放牧的牧场中捻转血矛线虫幼虫的污染显著降低。接种动物血浆中具有高水平的疫苗抗原特异性IgG1和IgG2抗体,而对照羊的这些反应非常低。接种组的IgG1滴度与虫卵计数呈负相关,但IgG2滴度并非如此。全身IgA和IgE水平保持较低,但在实验接近尾声时两组均有所升高,这很可能是由于接触了来自牧场的自然感染。结果表明,H11和H-gal-GP表现得像“隐蔽”抗原,能产生高水平的保护作用,可能是通过涉及抗体,尤其是IgG1的机制介导的。得出的结论是,如果用H11或H-gal-GP中存在的蛋白质的重组形式能获得类似的保护效果,那么商业化的血矛线虫疫苗的前景是真实的。