Li Qian, Jiang Yiqian, Zheng Min, Sun Xuefei, Hui Lili, Zhang Yanyan, Yue Huixian, Qi Yu, Li Siqi, Ke Junnan, Li Qixuan, Ma Boli, Jia Xiaoying, Wang Fengjie, Mi Lijuan, Zhang Shoufeng, Miao Faming, Wang Shuchao, Zhang Fei, Chen Teng, Hu Rongliang
Key Laboratory of Prevention & Control for African Swine Fever and Other Major Pig Diseases, Ministry of Agriculture and Rural Affairs, Changchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun 130122, China.
Microorganisms. 2024 Dec 13;12(12):2590. doi: 10.3390/microorganisms12122590.
African Swine Fever (ASF) is a highly contagious viral disease threatening the global pig industry. Currently, only two gene-deleted live attenuated vaccines are approved, exclusively in Vietnam, and their long-term effectiveness and safety are unproven, prompting the need for safer alternatives. This study assessed a cocktail of African Swine Fever Virus (ASFV) antigens delivered via a recombinant Newcastle Disease Virus (rNDV) vector against the genotype II ASFV-SY18. Antigens pB602L, pEP84R, and p22 (pKP177R) were selected based on virus neutralization and lymphocyte proliferation assays in mice and combined with capsid protein p72 (pB646L) for vaccination and challenge in pigs. The antigen cocktail delayed ASF symptoms by 3-4 days but did not prevent the lethal ASFV-SY18 infection. Significant ASFV-specific gamma interferon (IFN-γ) positive responses and NDV antibodies were detected post-inoculation, showing an induced immune response, though ASFV-specific p72 antibodies were absent. The cocktail did not cause cytokine imbalance, indicating the vector's safety in pigs. Despite some delay in disease progression, the protection against genotype II ASFV was inadequate, underscoring the need to select more effective antigens and enhance immune responses for virus-vectored vaccines.
非洲猪瘟(ASF)是一种极具传染性的病毒性疾病,威胁着全球养猪业。目前,仅有两种基因缺失的减毒活疫苗获得批准,且仅在越南获批使用,其长期有效性和安全性尚未得到证实,因此需要更安全的替代疫苗。本研究评估了一种通过重组新城疫病毒(rNDV)载体递送的非洲猪瘟病毒(ASFV)抗原鸡尾酒,用于对抗II型ASFV - SY18。基于小鼠体内的病毒中和试验和淋巴细胞增殖试验,选择了抗原pB602L、pEP84R和p22(pKP177R),并与衣壳蛋白p72(pB646L)联合用于猪的疫苗接种和攻毒试验。该抗原鸡尾酒使ASF症状延迟了3 - 4天,但未能预防致死性的ASFV - SY18感染。接种后检测到显著的ASFV特异性γ干扰素(IFN - γ)阳性反应和新城疫病毒抗体,表明诱导了免疫反应,不过未检测到ASFV特异性p72抗体。该鸡尾酒未导致细胞因子失衡,表明该载体对猪具有安全性。尽管疾病进展有所延迟,但针对II型ASFV的保护作用不足,这突出表明需要选择更有效的抗原并增强病毒载体疫苗的免疫反应。