Okita Go, Suenaga Kiyotaka, Sakaguchi Masashi, Murakami Toshio
Research Department, KM Biologics Co., Ltd., Kikuchi, Kumamoto, Japan.
PLoS One. 2025 Mar 6;20(3):e0312205. doi: 10.1371/journal.pone.0312205. eCollection 2025.
To generate a novel oncolytic vaccinia virus with improved safety and productivity, the genome of smallpox vaccine strain LC16m8 was modified by a bacterial artificial chromosome system. By using LC16m8, a replicating virus homologous to the target virus, as a helper virus for the bacterial artificial chromosome system, we successfully recovered genome-edited infectious viruses. Oncolytic viruses with limited growth in normal cells were obtained by deleting the genes for vaccinia virus growth factor (VGF), extracellular signal-regulated kinase-activating protein (O1L), and ribonucleotide reductase (RNR) present in the viral genome. Furthermore, the amino acid residues of seven proteins involved in extracellular enveloped virus virion formation were replaced to the IHD-J strain sequence, which is known to highly express extracellular enveloped virus. In cultured cancer cells (HeLa), these modified viruses showed cytotoxicity and increased productivity, but it was confirmed that the cytotoxicity was suppressed in normal cells (normal human dermal fibroblasts). For in vivo safety evaluation, a modified virus (MD-RVV-ΔRR-EEV6) in which the VGF, O1L, and RNR genes of LC16m8 were deleted and the genes of six extracellular enveloped virus-associated proteins were replaced with sequences derived from IHD-J strain, and another modified virus (MD-RVV) lacking only the VGF and O1L were administered intravenously to severe combined immunodeficiency mice. In the MD-RVV administration, animals in all dose groups died by 40 days after virus administration. On the other hand, after MD-RVV-ΔRR-EEV6 administration, 3 out of 5 animals in the high and medium dose groups and all animals in the low dose group were still alive by day 71, the end of the observation period. These results demonstrate that genome editing of oncolytic vaccinia virus can delete genes involved in viral replication to improve safety in normal cells, while replacing genes involved in maturation improves proliferative potential in cancer cells.
为了产生一种安全性和生产力得到提高的新型溶瘤痘苗病毒,利用细菌人工染色体系统对天花疫苗株LC16m8的基因组进行了改造。通过使用与目标病毒同源的复制型病毒LC16m8作为细菌人工染色体系统的辅助病毒,我们成功拯救出了基因组编辑的感染性病毒。通过删除病毒基因组中存在的痘苗病毒生长因子(VGF)、细胞外信号调节激酶激活蛋白(O1L)和核糖核苷酸还原酶(RNR)的基因,获得了在正常细胞中生长受限的溶瘤病毒。此外,将参与细胞外被膜病毒粒子形成的七种蛋白质的氨基酸残基替换为IHD-J株序列,已知该序列能高效表达细胞外被膜病毒。在培养的癌细胞(HeLa)中,这些改造后的病毒表现出细胞毒性并提高了生产力,但已证实在正常细胞(正常人皮肤成纤维细胞)中细胞毒性受到抑制。为了进行体内安全性评估,将LC16m8的VGF、O1L和RNR基因被删除且六种细胞外被膜病毒相关蛋白的基因被替换为源自IHD-J株序列的改造病毒(MD-RVV-ΔRR-EEV6),以及仅缺失VGF和O1L的另一种改造病毒(MD-RVV)静脉注射给严重联合免疫缺陷小鼠。在MD-RVV给药后,所有剂量组的动物在病毒给药后40天内死亡。另一方面,在MD-RVV-ΔRR-EEV6给药后,高剂量组和中剂量组的5只动物中有3只以及低剂量组的所有动物在观察期结束的第71天仍然存活。这些结果表明,溶瘤痘苗病毒的基因组编辑可以删除参与病毒复制的基因以提高在正常细胞中的安全性,同时替换参与成熟的基因可以提高在癌细胞中的增殖潜力。