Gómez Álex, Reina Ramsés
Departamento de Patología Animal, Universidad de Zaragoza, 177 Calle de Miguel Sevet, 50013 Zaragoza, Spain.
Instituto Agroalimentario de Aragón-IA2, Universidad de Zaragoza, 177 Calle de Miguel Sevet, 50013 Zaragoza, Spain.
Viruses. 2025 May 21;17(5):737. doi: 10.3390/v17050737.
Vaccination plays a pivotal role in the control and prevention of animal infectious diseases. However, no efficient and safe universal vaccines are currently registered for major pathogens such as influenza A virus, foot-and-mouth disease virus (FMDV), simian immunodeficiency virus (SIV), and small ruminant lentiviruses (SRLV). Here, we review the development of Sendai virus (SeV) vectors as a promising vaccine platform for animal diseases. Recombinant SeV vectors (rSeVv) possess several key features that make them highly suitable for developing vaccination strategies: (1) SeV has exclusively cytoplasmic replication cycle, therefore incapable of transforming host cells by integrating into the cellular genome, (2) rSeVv can accommodate large foreign gene/s inserts (~5 kb) with strong but adjustable transgene expression, (3) can be propagated to high titers in both embryonated chicken eggs and mammalian cell lines, (4) exhibits potent infectivity across a broad range of mammalian cells from different animals species, (5) undergo transient replication in the upper and lower respiratory tracts of non-natural hosts, (6) has not been associated with disease in pigs, non-humans primates, and small ruminants, ensuring a favorable safety profile, and (7) induce a robust innate and cellular immune responses. Preclinical and clinical studies using rSeVv-based vaccines against influenza A virus, FMDV, SIV, and SRLV have yielded promising results. Therefore, this review highlights the potential of rSeVv-based vaccine platforms as a valuable strategy for combating animal viruses.
疫苗接种在动物传染病的控制和预防中起着关键作用。然而,目前尚无针对甲型流感病毒、口蹄疫病毒(FMDV)、猴免疫缺陷病毒(SIV)和小反刍兽慢病毒(SRLV)等主要病原体的高效、安全通用疫苗注册。在此,我们综述了仙台病毒(SeV)载体作为一种有前景的动物疾病疫苗平台的发展情况。重组SeV载体(rSeVv)具有几个关键特性,使其非常适合用于制定疫苗接种策略:(1)SeV具有独特的细胞质复制周期,因此无法通过整合到细胞基因组中来转化宿主细胞;(2)rSeVv能够容纳大的外源基因插入片段(约5 kb),并具有强大但可调节的转基因表达;(3)可在鸡胚和哺乳动物细胞系中增殖至高滴度;(4)对来自不同动物物种的多种哺乳动物细胞具有强大的感染力;(5)在非天然宿主的上、下呼吸道中进行短暂复制;(6)在猪、非人灵长类动物和小反刍兽中未发现与疾病相关,确保了良好的安全性;(7)可诱导强烈的先天性和细胞免疫反应。使用基于rSeVv的疫苗针对甲型流感病毒、FMDV、SIV和SRLV进行的临床前和临床研究已取得了有前景的结果。因此,本综述强调了基于rSeVv的疫苗平台作为对抗动物病毒的一种有价值策略的潜力。