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Rabies Vaccination of 6-Week-Old Puppies Born to Immunized Mothers: A Randomized Controlled Trial in a High-Mortality Population of Owned, Free-Roaming Dogs

机译:狂犬病疫苗接种出生于免疫母亲的6周龄小狗:一个随机对照试验,在高死亡人口,自由漫游犬

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摘要

To achieve global elimination of human rabies from dogs by 2030, evidence-based strategies for effective dog vaccination are needed. Current guidelines recommend inclusion of dogs younger than 3 months in mass rabies vaccination campaigns, although available vaccines are only recommended for use by manufacturers in older dogs, ostensibly due to concerns over interference of maternally-acquired immunity with immune response to the vaccine. Adverse effects of vaccination in this age group of dogs have also not been adequately assessed under field conditions. In a single-site, owner-blinded, randomized, placebo-controlled trial in puppies born to mothers vaccinated within the previous 18 months in a high-mortality population of owned, free-roaming dogs in South Africa, we assessed immunogenicity and effect on survival to all causes of mortality of a single dose of rabies vaccine administered at 6 weeks of age. We found that puppies did not have appreciable levels of maternally-derived antibodies at 6 weeks of age (geometric mean titer 0.065 IU/mL, 95% CI 0.061−0.069; n = 346), and that 88% (95% CI 80.7−93.3) of puppies vaccinated at 6 weeks had titers ≥0.5 IU/mL 21 days later (n = 117). Although the average effect of vaccination on survival was not statistically significant (hazard ratio [HR] 1.35, 95% CI 0.83−2.18), this effect was modified by sex (p = 0.02), with the HR in females 3.09 (95% CI 1.24−7.69) and the HR in males 0.79 (95% CI 0.41−1.53). We speculate that this effect is related to the observed survival advantage that females had over males in the unvaccinated group (HR 0.27; 95% CI 0.11−0.70), with vaccination eroding this advantage through as-yet-unknown mechanisms.
机译:为了实现2030年从狗的全球消除人类狂犬病,需要为有效的有效狗疫苗接种的循证策略。目前的准则建议将狗纳入3个月的大众狂犬病疫苗接种活动,尽管只有可用的疫苗被推荐用于老年狗的制造商使用,因此由于对对疫苗免疫应答的免疫反应的潜入免疫的担忧而言。在该龄阶段,疫苗接种疫苗的不良反应也没有在现场条件下进行充分评估。在一个单独的,所有者蒙蔽,随机的,安慰剂对照试验中,在母亲在南非的高死亡率,在前18个月内接种疫苗,我们评估了免疫原性和影响在6周龄在6周内给药的单剂量狂犬病疫苗的所有原因的生存。我们发现小狗在6周龄(几何平均滴度0.065 IU / ml,95%CI 0.061-0.069; n = 346),88%(95%CI 80.7- 93.3)在6周内接种疫苗的幼犬滴度≥0.5IU / ml 21天(n = 117)。虽然疫苗接种对存活的平均效果没有统计学意义(危害比[HR] 1.35,95%CI 0.83-2.18),但是通过性(P = 0.02)修饰这种效果,女性3.09(95%CI) 1.24-7.69)和MALES 0.79的HR(95%CI 0.41-1.53​​)。我们推测,这种效果与观察到的生存优势有关,雌性在未接触的群体中有雌性(HR 0.27; 95%CI 0.11-0.70),通过尚不清楚的机制侵蚀这种优势。

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