Department of Biological and Health Sciences, Texas A&M University Kingsville, Kingsville, TX, USA.
Department of Anatomy and Physiology, Kansas State University, Manhattan, KS, USA.
Plant Biotechnol J. 2019 Feb;17(2):410-420. doi: 10.1111/pbi.12986. Epub 2018 Aug 10.
Classical Swine Fever Virus (CSFV) causes classical swine fever, a highly contagious hemorrhagic fever affecting both feral and domesticated pigs. Outbreaks of CSF in Europe, Asia, Africa and South America had significant adverse impacts on animal health, food security and the pig industry. The disease is generally contained by prevention of exposure through import restrictions (e.g. banning import of live pigs and pork products), localized vaccination programmes and culling of infected or at-risk animals, often at very high cost. Current CSFV-modified live virus vaccines are protective, but do not allow differentiation of infected from vaccinated animals (DIVA), a critical aspect of disease surveillance programmes. Alternatively, first-generation subunit vaccines using the viral protein E2 allow for use of DIVA diagnostic tests, but are slow to induce a protective response, provide limited prevention of vertical transmission and may fail to block viral shedding. CSFV E2 subunit vaccines from a baculovirus/insect cell system have been developed for several vaccination campaigns in Europe and Asia. However, this expression system is considered expensive for a veterinary vaccine and is not ideal for wide-spread deployment. To address the issues of scalability, cost of production and immunogenicity, we have employed an Agrobacterium-mediated transient expression platform in Nicotiana benthamiana and formulated the purified antigen in novel oil-in-water emulsion adjuvants. We report the manufacturing of adjuvanted, plant-made CSFV E2 subunit vaccine. The vaccine provided complete protection in challenged pigs, even after single-dose vaccination, which was accompanied by strong virus neutralization antibody responses.
经典猪瘟病毒(Classical Swine Fever Virus,CSFV)引起经典猪瘟,是一种高度传染性的出血热,影响野生和家养猪。欧洲、亚洲、非洲和南美洲的 CSF 爆发对动物健康、食品安全和养猪业造成了重大不利影响。该疾病通常通过进口限制(例如禁止进口活猪和猪肉产品)、局部疫苗接种计划和淘汰感染或处于风险中的动物来预防接触来控制,这通常需要付出很高的代价。目前的 CSFV 改良活病毒疫苗具有保护作用,但不能区分感染动物和接种疫苗动物(DIVA),这是疾病监测计划的一个关键方面。另一方面,使用病毒蛋白 E2 的第一代亚单位疫苗允许使用 DIVA 诊断测试,但诱导保护反应缓慢,对垂直传播的预防有限,并且可能无法阻止病毒脱落。几种欧洲和亚洲的疫苗接种运动已经开发了来自杆状病毒/昆虫细胞系统的 CSFV E2 亚单位疫苗。然而,该表达系统被认为对兽医疫苗来说成本过高,并且不适合广泛部署。为了解决可扩展性、生产成本和免疫原性问题,我们在本氏烟中使用农杆菌介导的瞬时表达平台,并在新型油包水乳剂佐剂中配制纯化抗原。我们报告了添加佐剂的、植物生产的 CSFV E2 亚单位疫苗的制造。该疫苗在接种挑战的猪中提供了完全保护,即使在单次接种后也是如此,同时还伴有强烈的病毒中和抗体反应。