Ura Takehiro, Okuda Kenji, Shimada Masaru
Department of Molecular Biodefense Research, Yokohama City University Graduate School of Medicine, Yokohama, Kanagawa Prefecture 236-0004, Japan.
Vaccines (Basel). 2014 Jul 29;2(3):624-41. doi: 10.3390/vaccines2030624.
Viral vectors are promising tools for gene therapy and vaccines. Viral vector-based vaccines can enhance immunogenicity without an adjuvant and induce a robust cytotoxic T lymphocyte (CTL) response to eliminate virus-infected cells. During the last several decades, many types of viruses have been developed as vaccine vectors. Each has unique features and parental virus-related risks. In addition, genetically altered vectors have been developed to improve efficacy and safety, reduce administration dose, and enable large-scale manufacturing. To date, both successful and unsuccessful results have been reported in clinical trials. These trials provide important information on factors such as toxicity, administration dose tolerated, and optimized vaccination strategy. This review highlights major viral vectors that are the best candidates for clinical use.
病毒载体是基因治疗和疫苗领域颇具前景的工具。基于病毒载体的疫苗无需佐剂即可增强免疫原性,并诱导强大的细胞毒性T淋巴细胞(CTL)反应以清除病毒感染细胞。在过去几十年中,许多类型的病毒已被开发用作疫苗载体。每种病毒都有其独特的特征以及与亲本病毒相关的风险。此外,已开发出基因改造载体以提高疗效和安全性、降低给药剂量并实现大规模生产。迄今为止,临床试验中既有成功的结果,也有失败的结果。这些试验提供了关于毒性、耐受给药剂量和优化疫苗接种策略等因素的重要信息。本综述重点介绍了最适合临床应用的主要病毒载体。