Yang Tao, Yuan Yi, Ma Feng
National Key Laboratory of Immunity and Inflammation, and CAMS Key Laboratory of Synthetic Biology Regulatory Elements, Suzhou Institute of Systems Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, Suzhou, China.
Methods Mol Biol. 2025;2940:165-171. doi: 10.1007/978-1-0716-4615-1_15.
Vesicular stomatitis virus (VSV), a negative-sense RNA virus, has emerged as a versatile platform for oncolytic virotherapy and vaccine development. Numerous advantages, such as a broad host range, rapid replication, and simple and easily modifiable genomes, make it an attractive candidate for both the treatment and prevention of infectious diseases and tumors. Advances in molecular biology techniques, particularly reverse genetics and synthetic biology, have facilitated the precise engineering of VSV genomes, thereby significantly expanding their applications in cancer therapeutics. One of the most common antitumor strategies is to promote tumor cell death. Numerous studies have shown that engineered VSV with cell death elements has considerable antitumor efficacy. This chapter provides a comprehensive overview of VSV engineering techniques, focusing specifically on the incorporation of the proapoptotic gene XAF1, along with detailed experimental procedures. The goal of these approaches is to increase the efficacy of VSV in antitumor immunity and other therapeutic domains.
水泡性口炎病毒(VSV)是一种负链RNA病毒,已成为溶瘤病毒疗法和疫苗开发的通用平台。它具有许多优势,如宿主范围广、复制迅速、基因组简单且易于修饰,使其成为治疗和预防传染病及肿瘤的有吸引力的候选者。分子生物学技术的进步,特别是反向遗传学和合成生物学,促进了VSV基因组的精确工程改造,从而显著扩大了其在癌症治疗中的应用。最常见的抗肿瘤策略之一是促进肿瘤细胞死亡。大量研究表明,带有细胞死亡元件的工程化VSV具有相当的抗肿瘤功效。本章全面概述了VSV工程技术,特别关注促凋亡基因XAF1的整合,并给出了详细的实验步骤。这些方法的目标是提高VSV在抗肿瘤免疫和其他治疗领域的功效。