Georg-Speyer-Haus, 60596 Frankfurt am Main, Germany.
J Mol Med (Berl). 2012 Aug;90(8):959-70. doi: 10.1007/s00109-012-0863-6.
Among oncolytic viruses, the vesicular stomatitis virus (VSV) is especially potent and a highly promising agent for the treatment of cancer. But, even though effective against multiple tumor entities in preclinical animal models, replication-competent VSV exhibits inherent neurovirulence, which has so far hindered clinical development. To overcome this limitation, replication-defective VSV vectors for cancer gene therapy have been tested and proven to be safe. However, gene delivery was inefficient and only minor antitumor efficacy was observed. Here, we present semireplication-competent vector systems for VSV (srVSV), composed of two trans-complementing, propagation-deficient VSV vectors. The de novo generated deletion mutants of the two VSV polymerase proteins P (phosphoprotein) and L (large catalytic subunit), VSVΔP and VSVΔL respectively, were used mutually or in combination with VSVΔG vectors. These srVSV systems copropagated in vitro and in vivo without recombinatory reversion to replication-competent virus. The srVSV systems were highly lytic for human glioblastoma cell lines, spheroids, and subcutaneous xenografts. Especially the combination of VSVΔG/VSVΔL vectors was as potent as wild-type VSV (VSV-WT) in vitro and induced long-term tumor regression in vivo without any associated adverse effects. In contrast, 90% of VSV-WT-treated animals succumbed to neurological disease shortly after tumor clearance. Most importantly, even when injected into the brain, VSVΔG/VSVΔL did not show any neurotoxicity. In conclusion, srVSV is a promising platform for virotherapeutic approaches and also for VSV-based vector vaccines, combining improved safety with an increased coding capacity for therapeutic transgenes, potentially allowing for multipronged approaches.
在溶瘤病毒中,水疱性口炎病毒(VSV)尤为有效,是治疗癌症的极具前景的药物。但是,尽管在临床前动物模型中对多种肿瘤实体有效,但具有复制能力的 VSV 表现出固有的神经毒性,这迄今为止阻碍了其临床开发。为了克服这一限制,已对用于癌症基因治疗的复制缺陷型 VSV 载体进行了测试,并已证明其安全。然而,基因传递效率低下,仅观察到轻微的抗肿瘤疗效。在这里,我们提出了 VSV 的半复制型载体系统(srVSV),由两个互补的、无复制能力的 VSV 载体组成。两个 VSV 聚合酶蛋白 P(磷蛋白)和 L(大催化亚基)的从头生成缺失突变体,即 VSVΔP 和 VSVΔL,分别被相互使用或与 VSVΔG 载体组合使用。这些 srVSV 系统在体外和体内共同繁殖,而不会重新恢复为具有复制能力的病毒。srVSV 系统对人神经胶质瘤细胞系、球体和皮下异种移植物高度溶瘤。特别是 VSVΔG/VSVΔL 载体的组合在体外与野生型 VSV(VSV-WT)一样有效,并在体内诱导长期肿瘤消退而没有任何相关的不良反应。相比之下,90%的 VSV-WT 治疗的动物在肿瘤清除后不久因神经疾病而死亡。最重要的是,即使注入大脑,VSVΔG/VSVΔL 也没有显示出任何神经毒性。总之,srVSV 是一种很有前途的溶瘤病毒治疗方法和基于 VSV 的载体疫苗平台,在提高安全性的同时增加了治疗性转基因的编码能力,可能允许采用多种方法。