Tripathy D N
Department of Veterinary Pathobiology, University of Illinois, Urbana 61802, USA.
Adv Vet Med. 1999;41:463-80. doi: 10.1016/s0065-3519(99)80035-4.
Several small and large viruses (e.g., adenovirus, poxvirus, and herpesviruses) have been investigated as vaccine vectors. Each viral system has its advantages and disadvantages. One major advantage for viral vector vaccines is their ability to elicit a protective cell-mediated immunity as well as a humoral response to the antigen delivered by the vector. One major problem to using recombinant viruses as vaccines is the pathogenic potential of the parent virus. Therefore, it is important that along with the optimal expression of the foreign genes and ability to provide protection, the pathogenicity of the vector virus must be reduced during genetic manipulation without affecting its multiplication. The requirements to develop a viral vector, for example, swinepox virus, are a cell culture system that will support the growth of the virus, a suitable nonessential region(s) in the virus genome for insertion of foreign DNA so that virus replication is not affected, a foreign gene(s) that encodes for an immunogenic protein of a swine pathogen, strong transcriptional regulatory elements (promoters) necessary for optimal expression of the foreign genes, a procedure for delivering the foreign gene(s) into the nonessential locus, and a convenient method of distinguishing the recombinant viruses from the parent wild-type virus. Using this methodology, recombinant swinepox virus vaccines expressing pseudorabies virus antigens have been developed and shown to provide protection against challenge. These studies and evidence of local infection of the oral tract by swinepox virus indicate its potential as a recombinant vector for providing immunity against various swine pathogens including those that infect the respiratory and gastrointestinal tracts.
几种大小不同的病毒(如腺病毒、痘病毒和疱疹病毒)已被研究用作疫苗载体。每个病毒系统都有其优缺点。病毒载体疫苗的一个主要优点是它们能够引发保护性细胞介导免疫以及对载体传递的抗原产生体液反应。使用重组病毒作为疫苗的一个主要问题是亲本病毒的致病潜力。因此,重要的是,除了外源基因的最佳表达和提供保护的能力外,载体病毒的致病性在基因操作过程中必须降低,同时不影响其增殖。开发一种病毒载体(例如猪痘病毒)的要求包括:一个能够支持病毒生长的细胞培养系统、病毒基因组中适合插入外源DNA的非必需区域(以便不影响病毒复制)、编码猪病原体免疫原性蛋白的外源基因、外源基因最佳表达所需的强转录调控元件(启动子)、将外源基因导入非必需位点的程序,以及一种区分重组病毒和亲本野生型病毒的便捷方法。利用这种方法,已经开发出表达伪狂犬病病毒抗原的重组猪痘病毒疫苗,并证明其能提供针对攻毒的保护。这些研究以及猪痘病毒在口腔局部感染的证据表明,它作为重组载体具有为抵抗包括感染呼吸道和胃肠道的病原体在内的各种猪病原体提供免疫的潜力。