Goatley Lynnette C, Reis Ana Luisa, Portugal Raquel, Goldswain Hannah, Shimmon Gareth L, Hargreaves Zoe, Ho Chak-Sum, Montoya María, Sánchez-Cordón Pedro J, Taylor Geraldine, Dixon Linda K, Netherton Christopher L
The Pirbright Institute, Ash Road, Pirbright, Surrey GU24 0NF, UK.
Gift of Hope Organ and Tissue Donor Network, Itasca, IL 60143, USA.
Vaccines (Basel). 2020 May 18;8(2):234. doi: 10.3390/vaccines8020234.
Classical approaches to African swine fever virus (ASFV) vaccine development have not been successful; inactivated virus does not provide protection and use of live attenuated viruses generated by passage in tissue culture had a poor safety profile. Current African swine fever (ASF) vaccine research focuses on the development of modified live viruses by targeted gene deletion or subunit vaccines. The latter approach would be differentiation of vaccinated from infected animals (DIVA)-compliant, but information on which viral proteins to include in a subunit vaccine is lacking. Our previous work used DNA-prime/vaccinia-virus boost to screen 40 ASFV genes for immunogenicity, however this immunization regime did not protect animals after challenge. Here we describe the induction of both antigen and ASFV-specific antibody and cellular immune responses by different viral-vectored pools of antigens selected based on their immunogenicity in pigs. Immunization with one of these pools, comprising eight viral-vectored ASFV genes, protected 100% of pigs from fatal disease after challenge with a normally lethal dose of virulent ASFV. This data provide the basis for the further development of a subunit vaccine against this devastating disease.
非洲猪瘟病毒(ASFV)疫苗研发的传统方法尚未成功;灭活病毒无法提供保护,而在组织培养中传代产生的减毒活病毒安全性较差。目前非洲猪瘟(ASF)疫苗研究聚焦于通过靶向基因缺失开发改良活病毒或亚单位疫苗。后一种方法符合区分疫苗接种动物和感染动物(DIVA)的要求,但缺乏关于亚单位疫苗应包含哪些病毒蛋白的信息。我们之前的工作采用DNA初免/痘苗病毒加强免疫来筛选40个ASFV基因的免疫原性,然而这种免疫方案在攻毒后并不能保护动物。在此,我们描述了基于在猪体内的免疫原性选择的不同病毒载体抗原库诱导抗原以及ASFV特异性抗体和细胞免疫反应的情况。用其中一个包含八个病毒载体ASFV基因的抗原库进行免疫,在用正常致死剂量的强毒ASFV攻毒后,100%的猪免受致命疾病侵害。这些数据为进一步研发针对这种毁灭性疾病的亚单位疫苗奠定了基础。