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DNA-based vaccine protects against zoonotic schistosomiasis in water buffalo

机译:基于DNA的疫苗可预防水牛的人畜共患血吸虫病

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摘要

Schistosomiasis japonica is an endemic, zoonotic disease of major public health importance in China where water buffaloes account for approximately 75% of disease transmission. Interventions that reduce schistosome infection in water buffaloes will enhance their health simultaneously reducing disease transmission to humans. While chemotherapy has proved successful, it requires continued time consuming and expensive mass treatments. A more sustainable option would be development of vaccines that reduce transmission of S. japonicum from bovines to replace bovine chemotherapy. We performed two randomized double blind trials in water buffaloes to determine if DNA vaccines encoding triose-phosphate isomerase (SjCTPI), or the tetraspanin 23 kDa integral membrane protein (SjC23), alone or fused to bovine heat shock protein 70 (Hsp70) could induce a level of immunity conducive to long-term sustainable control. Groups of water buffaloes (15/group) received three intramuscular injections, 4 weeks apart. Booster immunizations were co-administered with a plasmid DNA encoding IL-12. Four weeks after the last injection, water buffaloes were challenged with 1000 cercariae, and vaccine efficacy analyzed 8 weeks later. Water buffaloes vaccinated with SjCTPI-Hsp70 or SjCTPI plasmids had worm burdens reduced by 51.2% and 41.5%, respectively. Importantly, fecal miracidial hatching was reduced by 52.1% and 33.2% respectively compared to control vaccinated water buffaloes. Vaccination with SjC23-Hsp70 and SjC23 plasmids reduced worm burdens by 50.9% and 45.5%, respectively, and fecal miracidial hatching by 52.0% and 47.4%. A mathematical model of schistosome transmission predicts that schistosome vaccines capable of reducing water buffaloes' fecal egg output by 45%, alone or in conjunction with praziquantel treatment, will lead to a significant reduction in transmission of schistosomiasis. Both DNA vaccines tested here exceed this hypothetical level. Indeed, mathematical modeling of SjCTPI-Hsp70 and SjC23-Hsp70 alone and in conjunction with human chemotherapy showed a significant reduction in transmission almost to the point of elimination.
机译:在中国,水牛约占疾病传播的75%,日本血吸虫病是一种具有重要公共卫生意义的地方性人畜共患病。减少水牛血吸虫感染的干预措施将增强它们的健康,同时减少疾病向人类的传播。尽管化学疗法已被证明是成功的,但它需要持续的时间和昂贵的大规模治疗。更具可持续性的选择是开发疫苗,以减少日本血吸虫从牛的传播,以取代牛的化学疗法。我们在水牛中进行了两项随机双盲试验,以确定单独或与牛热激蛋白70(Hsp70)融合的编码三糖磷酸异构酶(SjCTPI)或四跨膜蛋白23 kDa整合膜蛋白(SjC23)的DNA疫苗是否可以诱导有助于长期可持续控制的免疫力水平。水牛组(每组15只)接受了3次肌肉注射,相隔4周。加强免疫与编码IL-12的质粒DNA共同施用。最后一次注射后四周,对水牛用1000只尾c进行攻击,并在8周后分析了疫苗效力。接种SjCTPI-Hsp70或SjCTPI质粒的水牛的蠕虫负担分别减少了51.2%和41.5%。重要的是,与对照疫苗接种的水牛相比,粪便mir虫孵化率分别降低了52.1%和33.2%。用SjC23-Hsp70和SjC23质粒接种疫苗后,蠕虫负担分别降低了50.9%和45.5%,粪便虫孵化分别降低了52.0%和47.4%。血吸虫病传播的数学模型预测,能够单独或与吡喹酮治疗联用的能够将水牛粪便卵产量降低45%的血吸虫病疫苗,将导致血吸虫病传播的显着减少。在此测试的两种DNA疫苗均超出了这一假设水平。确实,单独的SjCTPI-Hsp70和SjC23-Hsp70以及与人类化学疗法结合的数学模型显示,传播途径明显减少,几乎消除了。

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