Zoetis, Veterinary Medicine Research and Development, 1930 Zaventem, Belgium.
Vaccine. 2013 Jun 28;31(31):3131-4. doi: 10.1016/j.vaccine.2013.05.041. Epub 2013 May 23.
Although effective vaccines have been developed against the common Leptospira serovars, they are still reported in clinical cases, while others are increasingly prevalent. The results from four challenge studies following vaccination of dogs with a new combination vaccine (DHPPi/L4R) containing inactivated L. serovars, L. canicola, L. icterohaemorrhagiae, L. bratislava and L. grippotyphosa conducted to satisfy the requirements of the European Pharmacopoeia monograph (01/2008:0447), are reported. Six week old dogs received two vaccinations, three weeks apart, and were challenged 25 days later with different isolates of the L. serovars. Clinical observations were recorded, and blood, urine and tissue samples were collected for analysis. Following challenge, non-vaccinated dogs demonstrated various clinical signs, while no vaccinated dogs were affected; significant differences in mean clinical scores were observed. Measurable antibody titres to each Leptospira antigen were seen in vaccinated dogs 21 days following the first vaccination, with further increases in antibody titres observed following challenge with the respective Leptospira strain. Non-vaccinated dogs remained seronegative until challenge. Leptospira were re-isolated from the blood, urine, kidney and liver of all non-vaccinated dogs following challenge. In contrast no vaccinated dogs had Leptospira re-isolated from the same tissues. Significant differences were seen in number of days with positive isolation (blood and urine) and in number of dogs with positive samples (kidney and liver). In conclusion, vaccination of dogs with the new vaccine induces protective immunity 25 days after second vaccination with protection against infection, renal infection and clinical signs following challenge.
尽管针对常见钩端螺旋体血清型已开发出有效的疫苗,但在临床病例中仍有报告,而其他血清型则越来越普遍。本研究报告了四项挑战研究的结果,这些研究是在对使用新型组合疫苗(DHPPi/L4R)对犬进行免疫接种后进行的,该疫苗含有灭活的钩端螺旋体血清型、犬型钩端螺旋体、黄疸出血型钩端螺旋体、布拉迪斯拉发钩端螺旋体和流感伤寒型钩端螺旋体,以满足欧洲药典专论(01/2008:0447)的要求。6 周龄的犬接受两次疫苗接种,间隔 3 周,然后在 25 天后用不同的钩端螺旋体血清型分离株进行挑战。记录临床观察结果,并采集血液、尿液和组织样本进行分析。挑战后,未接种疫苗的犬表现出各种临床症状,而接种疫苗的犬没有受到影响;观察到平均临床评分有显著差异。在第一次接种疫苗后 21 天,接种疫苗的犬对每种钩端螺旋体抗原均产生可测量的抗体滴度,在分别用相应的钩端螺旋体菌株进行挑战后,抗体滴度进一步增加。未接种疫苗的犬在挑战前仍呈血清阴性。挑战后,所有未接种疫苗的犬的血液、尿液、肾脏和肝脏中均重新分离出钩端螺旋体。相比之下,没有接种疫苗的犬从相同组织中未重新分离出钩端螺旋体。在阳性分离(血液和尿液)的天数和阳性样本(肾脏和肝脏)的犬数方面均观察到显著差异。总之,在第二次接种疫苗后 25 天,对犬进行新型疫苗接种可诱导保护性免疫,从而在挑战后预防感染、肾脏感染和临床症状。