Maki Joanne, Guiot Anne-Laure, Aubert Michel, Brochier Bernard, Cliquet Florence, Hanlon Cathleen A, King Roni, Oertli Ernest H, Rupprecht Charles E, Schumacher Caroline, Slate Dennis, Yakobson Boris, Wohlers Anne, Lankau Emily W
Boehringer Ingelheim Animal Health, 1730 Olympic Drive, Athens, GA, 30601, USA.
Conseils en Pharmacie et Biologie, Sainte Foy les, Lyon, France.
Vet Res. 2017 Sep 22;48(1):57. doi: 10.1186/s13567-017-0459-9.
RABORAL V-RG is an oral rabies vaccine bait that contains an attenuated ("modified-live") recombinant vaccinia virus vector vaccine expressing the rabies virus glycoprotein gene (V-RG). Approximately 250 million doses have been distributed globally since 1987 without any reports of adverse reactions in wildlife or domestic animals since the first licensed recombinant oral rabies vaccine (ORV) was released into the environment to immunize wildlife populations against rabies. V-RG is genetically stable, is not detected in the oral cavity beyond 48 h after ingestion, is not shed by vaccinates into the environment, and has been tested for thermostability under a range of laboratory and field conditions. Safety of V-RG has been evaluated in over 50 vertebrate species, including non-human primates, with no adverse effects observed regardless of route or dose. Immunogenicity and efficacy have been demonstrated under laboratory and field conditions in multiple target species (including fox, raccoon, coyote, skunk, raccoon dog, and jackal). The liquid vaccine is packaged inside edible baits (i.e., RABORAL V-RG, the vaccine-bait product) which are distributed into wildlife habitats for consumption by target species. Field application of RABORAL V-RG has contributed to the elimination of wildlife rabies from three European countries (Belgium, France and Luxembourg) and of the dog/coyote rabies virus variant from the United States of America (USA). An oral rabies vaccination program in west-central Texas has essentially eliminated the gray fox rabies virus variant from Texas with the last case reported in a cow during 2009. A long-term ORV barrier program in the USA using RABORAL V-RG is preventing substantial geographic expansion of the raccoon rabies virus variant. RABORAL V-RG has also been used to control wildlife rabies in Israel for more than a decade. This paper: (1) reviews the development and historical use of RABORAL V-RG; (2) highlights wildlife rabies control programs using the vaccine in multiple species and countries; and (3) discusses current and future challenges faced by programs seeking to control or eliminate wildlife rabies.
RABORAL V-RG是一种口服狂犬病疫苗诱饵,它含有一种减毒(“改良活”)重组痘苗病毒载体疫苗,该疫苗表达狂犬病病毒糖蛋白基因(V-RG)。自1987年以来,全球已分发了约2.5亿剂,自第一种获得许可的重组口服狂犬病疫苗(ORV)投放环境以免疫野生动物群体抵抗狂犬病以来,没有关于野生动物或家畜出现不良反应的报告。V-RG基因稳定,在摄入后48小时内口腔中检测不到,接种动物不会将其传播到环境中,并且已在一系列实验室和野外条件下进行了热稳定性测试。V-RG的安全性已在包括非人灵长类动物在内的50多种脊椎动物物种中进行了评估,无论给药途径或剂量如何,均未观察到不良反应。在实验室和野外条件下,已在多个目标物种(包括狐狸、浣熊、郊狼、臭鼬、貉和豺)中证明了其免疫原性和有效性。液体疫苗包装在可食用诱饵(即RABORAL V-RG,疫苗诱饵产品)内,这些诱饵被分发到野生动物栖息地供目标物种食用。RABORAL V-RG的野外应用促使三个欧洲国家(比利时、法国和卢森堡)消除了野生动物狂犬病,并使美国消除了犬/郊狼狂犬病病毒变种。得克萨斯州中西部的一项口服狂犬病疫苗接种计划已基本消除了得克萨斯州的灰狐狂犬病病毒变种,最后一例病例报告于2009年一头奶牛身上。美国一项使用RABORAL V-RG的长期ORV屏障计划正在阻止浣熊狂犬病病毒变种的大规模地理扩张。RABORAL V-RG也已用于以色列控制野生动物狂犬病十多年。本文:(1)回顾了RABORAL V-RG的研发和历史使用情况;(2)重点介绍了在多个物种和国家使用该疫苗的野生动物狂犬病控制计划;(3)讨论了旨在控制或消除野生动物狂犬病的计划目前和未来面临的挑战。