VanHoy Grace, Carman Michelle, Habing Greg, Lakritz Jeffrey, Hinds C Austin, Niehaus Andrew, Kaplan Ray M, Marsh Antoinette E
Department of Veterinary Clinical Sciences, College of Veterinary Medicine, Ohio State University, Columbus, OH, 43210, United States.
Department of Veterinary Preventive Medicine, College of Veterinary Medicine, Ohio State University, Columbus, OH, 43210, United States.
Vet Parasitol. 2018 Mar 15;252:180-186. doi: 10.1016/j.vetpar.2018.02.014. Epub 2018 Feb 9.
Haemonchosis in camelids remains a challenging disease to treat, and prevention has become increasingly problematic due to widespread anthelmintic resistance. Barbervaxis an adjuvanted vaccine containing natural H-11, H-gal-GP antigens obtained from Haemonchus contortus adults via a proprietary process and solubilized in Quil A. This vaccine is approved for use in Australia, after demonstrating its safety and efficacy in sheep and goats. There are no published studies evaluating Barbervax in other ruminants/pseudoruminants such as camelids which can be parasitized with H. contortus. The vaccine utilizes a mixture of the parasite gut mucosal membrane enzymes including H-gal-GP and H11, involved in digesting a blood meal from the host. This study monitored the safety profile of the Barbervax vaccine in a group of adolescent alpacas. Although designed into the original study of vaccine efficacy, the experimental infection with viable H. contortus third stage larvae could not be completed due to lack of detectable significant variation of infection following experimental challenge. Twelve alpacas (158 + 15 days) were randomized to vaccination with Barbervax or no treatment. Three doses of Barbervax were administered at 3 week intervals and investigators involved in animal monitoring and sample collection were blinded to the groupings. Clinical pathologic parameters were evaluated 7 days before vaccination, and 1 and 2 months post-vaccination. Daily clinical observations were made and specific observations regarding the injection site and rectal temperatures were monitored in each alpaca twice daily for 1 week following vaccination. Fecal egg counts, packed cell volume, and total protein were monitored following challenge with 1500 H. contortus larvae on days 42, 46, and 50. An increase in rectal temperature for a duration of 2 days (range 2-4 days) was observed post-vaccination. Vaccinated alpacas were lethargic for 2-3 days following vaccination; however, they maintained an appetite and no visible or palpable injection site reactions were observed. Following the first vaccination, all animals maintained normal clinical pathologic parameters throughout the study period. The vaccinated animals did develop titers to the H. contortus antigen as measured by ELISA. In conclusion, the Barbervax vaccine demonstrated safety in this small group of young, healthy alpacas, but additional studies are required to evaluate the efficacy of the vaccine under field conditions in protecting alpacas against infection with H. contortus.
骆驼科动物的捻转血矛线虫病仍然是一种难以治疗的疾病,由于广泛存在的抗驱虫药现象,预防也变得越来越成问题。Barbervaxis一种佐剂疫苗,含有通过专有工艺从捻转血矛线虫成虫中获得并溶解在Quil A中的天然H-11、H-gal-GP抗原。该疫苗在证明其对绵羊和山羊的安全性和有效性后,已在澳大利亚获批使用。目前尚无已发表的研究评估Barbervax在其他可被捻转血矛线虫寄生的反刍动物/类反刍动物(如骆驼科动物)中的效果。该疫苗利用了包括H-gal-GP和H11在内的寄生虫肠道粘膜膜酶的混合物,这些酶参与消化来自宿主的血餐。本研究监测了Barbervax疫苗在一组青春期羊驼中的安全性。尽管在疫苗效力的原始研究中有所设计,但由于在实验性攻击后缺乏可检测到的显著感染差异,未能完成用活的捻转血矛线虫第三期幼虫进行的实验性感染。将12只羊驼(158±15天)随机分为接种Barbervax组或不治疗组。每隔3周接种三剂Barbervax,参与动物监测和样本采集的研究人员对分组情况不知情。在接种疫苗前7天、接种后1个月和2个月评估临床病理参数。每天进行临床观察,并在接种疫苗后的1周内,每天对每只羊驼的注射部位和直肠温度进行两次具体观察。在第42、46和50天用1500只捻转血矛线虫幼虫攻击后,监测粪便虫卵计数、红细胞压积和总蛋白。接种疫苗后观察到直肠温度升高持续2天(范围为2 - 4天)。接种疫苗的羊驼在接种后2 - 3天表现出嗜睡;然而,它们保持了食欲,且未观察到明显的或可触及的注射部位反应。在首次接种后,所有动物在整个研究期间的临床病理参数均保持正常。通过ELISA检测,接种疫苗的动物确实产生了针对捻转血矛线虫抗原的抗体滴度。总之,Barbervax疫苗在这一小群年轻、健康的羊驼中显示出安全性,但需要进一步研究以评估该疫苗在野外条件下保护羊驼免受捻转血矛线虫感染的效力。