首页> 外文OA文献 >The development and use of a vaccinia-rabies recombinant oral vaccine for the control of wildlife rabies; a link between Jenner and Pasteur.
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The development and use of a vaccinia-rabies recombinant oral vaccine for the control of wildlife rabies; a link between Jenner and Pasteur.

机译:开发和使用牛痘狂犬病重组口服疫苗来控制野生狂犬病;詹纳和巴斯德之间的联系。

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摘要

To improve both safety and stability of the oral vaccines used in the field to vaccinate foxes against rabies, a recombinant vaccinia virus, which expresses the immunizing G protein of rabies virus has been developed by inserting the cDNA which codes for the immunogenic glycoprotein of rabies virus into the thymidine kinase (TK) gene of the Copenhagen strain of vaccinia virus. The efficacy of this vaccine was tested by the oral route, primarily in foxes. The immunity conferred, a minimum of 12 months in cubs and 18 months in adult animals, corresponds to the duration of the protection required for vaccination of foxes in the field. Innocuity was tested in foxes, domestic animals, and in numerous European wild animal species that could compete with the red fox for the vaccine bait. No clinical signs or lesions were observed in any of the vaccinated animals during a minimum of 28 days post vaccination. Moreover, no transmission of immunizing doses of the recombinant occurred between foxes or other species tested. To study the stability of the vaccine strain, baits containing the vaccine were placed in the field. Despite considerable variations of environmental temperatures, the vaccine remained stable for at least one month. Because bait is taken within one month, it can be assumed that most animals taking the baits are effectively vaccinated. To test the field efficacy of the recombinant vaccine, large-scale campaigns of fox vaccination were set up in a 2200 km2 region of southern Belgium, were rabies was prevalent. A dramatic decrease in the incidence of rabies was noted after the campaigns. The recombinant is presently used to control wildlife rabies in the field both in several European countries and in the United States.
机译:为了提高用于狂犬病狐狸疫苗接种的口服疫苗的安全性和稳定性,通过插入编码狂犬病病毒免疫原性糖蛋白的cDNA,开发了表达狂犬病病毒免疫G蛋白的重组牛痘病毒。进入牛痘病毒哥本哈根株的胸苷激酶(TK)基因。通过口服途径(主要是在狐狸中)测试了该疫苗的功效。所赋予的免疫力,在幼崽中至少为12个月,在成年动物中至少为18个月,对应于田野中的狐狸疫苗接种所需的保护期。在狐狸,家畜以及许多可以与赤狐竞争诱饵的欧洲野生动物中测试了无辜性。在接种后至少28天内,未在任何接种过的动物中观察到临床症状或损伤。而且,在狐狸或其他测试物种之间没有发生免疫剂量重组体的传播。为了研究疫苗菌株的稳定性,将含有疫苗的诱饵置于野外。尽管环境温度变化很大,该疫苗仍可稳定稳定至少一个月。由于诱饵是在一个月之内服用的,因此可以假定大多数使用该诱饵的动物都已有效接种疫苗。为了测试重组疫苗的田间功效,在狂犬病流行的比利时南部2200 km2地区发起了大规模的狐狸疫苗接种运动。运动后,狂犬病发生率显着下降。目前,该重组体在几个欧洲国家和美国都用于野外控制狂犬病狂犬病。

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