首页> 外文期刊>Acta veterinaria scandinavica >Efficacy of rabies vaccines in dogs and cats and protection in a mouse model against European bat lyssavirus type 2
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Efficacy of rabies vaccines in dogs and cats and protection in a mouse model against European bat lyssavirus type 2

机译:狂犬病疫苗在猫狗中的功效以及在小鼠模型中针对欧洲2型蝙蝠狂犬病病毒的保护作用

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Background Rabies is preventable by pre- and/or post-exposure prophylaxis consisting of series of rabies vaccinations and in some cases the use of immunoglobulins. The success of vaccination can be estimated either by measuring virus neutralising antibodies or by challenge experiment. Vaccines based on rabies virus offer cross-protection against other lyssaviruses closely related to rabies virus. The aim was to assess the success of rabies vaccination measured by the antibody response in dogs (n?=?10,071) and cats (n?=?722), as well as to investigate the factors influencing the response to vaccination when animals failed to reach a rabies antibody titre of ≥?0.5?IU/ml. Another aim was to assess the level of protection afforded by a commercial veterinary rabies vaccine against intracerebral challenge in mice with European bat lyssavirus type 2 (EBLV-2) and classical rabies virus (RABV), and to compare this with the protection offered by a vaccine for humans. Results A significantly higher proportion of dogs (10.7%, 95% confidence interval CI 10.1–11.3) than cats (3.5%; 95% CI 2.3–5.0) had a vaccination antibody titre of 60?cm or larger resulted in a higher risk of failing to reach an antibody level of at least 0.5?IU/ml. When challenged with EBLV-2 and RABV, 80 and 100% of mice vaccinated with the veterinary rabies vaccine survived, respectively. When mice were vaccinated with the human rabies vaccine and challenged with EBLV-2, 75–80% survived, depending on the booster. All vaccinated mice developed sufficient to high titres of virus-neutralising antibodies (VNA) against RABV 21–22?days post-vaccination, ranging from 0.5 to 128?IU/ml. However, there was significant difference between antibody titres after vaccinating once in comparison to vaccinating twice (P Conclusions There was a significant difference between dogs and cats in their ability to reach a post vaccination antibody titre of ≥?0.5?IU/ml. Mice vaccinated with RABV-based rabies vaccines were partly cross-protected against EBLV-2, but there was no clear correlation between VNA titres and cross-protection against EBLV-2. Measurement of the RABV VNA titre can only be seen as a partial tool to estimate the cross-protection against other lyssaviruses. Booster vaccination is recommended for dogs and cats if exposed to infected bats.
机译:背景狂犬病可以通过暴露前和/或暴露后预防来预防,这些预防包括一系列的狂犬病疫苗接种,在某些情况下还可以使用免疫球蛋白。可以通过测量病毒中和抗体或通过攻击实验来评估疫苗接种的成功率。基于狂犬病病毒的疫苗对与狂犬病病毒密切相关的其他狂犬病病毒具有交叉保护作用。目的是评估通过抗体反应在犬(n = 10 071)和猫(n = 722)中检测到的狂犬病疫苗接种的成功率,并研究当动物未能接种时影响疫苗接种反应的因素。狂犬病抗体滴度达到≥0.5?IU / ml。另一个目的是评估在欧洲2型蝙蝠狂犬病病毒(EBLV-2)和经典狂犬病病毒(RABV)的小鼠中,商业兽医狂犬病疫苗提供的针对脑内攻击的保护水平,并将其与由人类疫苗。结果疫苗抗体效价为60?cm或更大的猫(3.5%; 95%CI为2.3–5.0)的狗(10.7%,95%置信区间CI 10.1–11.3)的比例显着更高,从而导致接种疫苗的风险更高。无法达到至少0.5?IU / ml的抗体水平。当用EBLV-2和RABV攻击时,分别有80%和100%的兽医狂犬病疫苗接种的小鼠存活。当给小鼠接种人类狂犬病疫苗并用EBLV-2攻击时,存活率高达75–80%,具体取决于加强剂量。所有接种疫苗的小鼠在接种疫苗后21-22天均能产生足够高滴度的针对RABV的病毒中和抗体(VNA),范围从0.5至128µIU / ml。但是,接种两次后的抗体滴度与接种两次后的抗体滴度之间存在显着差异(P结论在犬和猫之间,其达到≥0.5?IU / ml的疫苗后抗体滴度的能力存在显着差异。基于RABV的狂犬病疫苗对EBLV-2具有部分交叉保护,但VNA滴度与针对EBLV-2的交叉保护之间没有明显的相关性RABV VNA滴度的测量只能作为估算的部分工具如果暴露于受感染的蝙蝠,建议对猫和狗进行加强免疫接种。

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