Institute of Veterinary, Animal and Biomedical Sciences, Massey University, Palmerston North, New Zealand.
Prev Vet Med. 2012 Feb 1;103(2-3):136-44. doi: 10.1016/j.prevetmed.2011.08.010. Epub 2011 Sep 16.
A clinical trial was undertaken to assess the efficacy of Bovilis(®) Neoguard, a killed Neospora caninum tachyzoite vaccine on 5 commercial dairy farms in New Zealand with a history of Neospora-associated abortion. Cattle were enrolled in the trial at 30-60 days of gestation and randomly allocated to treatment or control groups. Treatment consisted of 5 mL doses of Bovilis Neoguard administered subcutaneously at enrolment then 4 weeks later. Isotonic saline was administered to the control group. Of 2246 cattle enrolled in the trial, 10.7% of cows and 12.6% of heifers were seropositive to N. caninum. Sampling of a randomly selected proportion of enrolled animals 6 weeks after the second treatment showed that 188/232 (81.0%) vaccinated with Bovilis(®) Neoguard had seroconverted, while 11/130 (8.5%) cows and 10/36 (27.8%) heifers in the control group had seroconverted. Forty-eight vaccinated and 63 control animals aborted. On one farm 12.5% of control animals and 6.1% of vaccinated animals aborted (vaccine efficacy 0.61; p=0.03). On another farm with a high level of abortion 8.4% of control animals and 8.7% of vaccinates aborted. On the remaining 3 farms fewer abortions occurred than expected. A modified Poisson regression approach was used to calculate relative risks for abortion and vertical transmission. Overall vaccine efficacy was 0.25 (p=0.12). Heifer replacement calves from the animals enrolled in the trial were sampled for antibodies to N. caninum at 6-9 months of age. Fourteen of 17 calves from vaccinated, seropositive cows were seropositive as were 13/23 calves from seropositive cows in the control group. The interaction between dam serostatus and treatment group was significant (p=0.05) with vaccination increasing the risk of vertical transmission. It was concluded that vaccination after conception prevented 61% abortions in one of five herds and that vaccination may have increased the risk of early embryonic death.
一项临床试验评估了 Bovilis(®)Neoguard,一种已杀死的刚地弓形虫速殖子疫苗,在新西兰的五家有弓形体相关流产史的商业化奶牛场中的效果。牛在妊娠 30-60 天时被纳入试验,并随机分配到治疗组或对照组。治疗组在入组时皮下注射 5 毫升 Bovilis Neoguard,然后在 4 周后再次注射。对照组给予等渗盐水。在 2246 头参加试验的牛中,10.7%的母牛和 12.6%的小母牛对刚地弓形虫呈血清阳性。在第二次治疗后 6 周对随机选择的部分入组动物进行采样,结果显示,188/232(81.0%)接种 Bovilis(®)Neoguard 的牛血清转化,而对照组 11/130(8.5%)的母牛和 10/36(27.8%)的小母牛血清转化。48 头接种疫苗的动物和 63 头对照组的动物流产。在一个农场中,对照组动物的流产率为 12.5%,接种疫苗的动物的流产率为 6.1%(疫苗效力 0.61;p=0.03)。在另一个流产率较高的农场中,对照组动物的流产率为 8.4%,接种疫苗的动物的流产率为 8.7%。在其余 3 个农场中,流产的动物数量低于预期。采用修正泊松回归方法计算流产和垂直传播的相对风险。总体疫苗效力为 0.25(p=0.12)。在 6-9 月龄时,从参加试验的动物中抽取后备小母牛血清样本,检测刚地弓形虫抗体。在血清阳性的接种母牛的 17 头小牛中,有 14 头呈血清阳性,在血清阳性的对照组母牛的 23 头小牛中,有 13 头呈血清阳性。母牛血清阳性状态和治疗组之间的相互作用具有统计学意义(p=0.05),接种疫苗增加了垂直传播的风险。研究结论认为,妊娠后接种疫苗可预防 5 个牛群中的 1 个中的 61%的流产,并且接种疫苗可能增加早期胚胎死亡的风险。