Development of an HSV-2 based oncolytic virus

基于 HSV-2 的溶瘤病毒的开发

• 批准号: 7579620
• 负责人: SHAUN XIAOLIU ZHANG
• 金额: $ 20.26万
• 依托单位: BAYLOR COLLEGE OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-12-01 至 2009-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7579620
• 关键词: Acute; Animal Model; Animals; Antineoplastic Agents; Antiviral Agents; Apoptosis; Binding; Cell Cycle; Cell membrane; Cells; Characteristics; Chemicals; Clinical; Clinical Trials; Clinical Trials Design; Cytolysis; Data; Decitabine; Development; Development Plans; Dichloroacetate; Disease; Energy Metabolism; Engineering; Future; Gene Delivery; Gene Expression; Generations; Genes; Giant Cells; Goals; Growth; Herpesvirus 1; Human Herpesvirus 2; Immune system; Immunity; In Vitro; Induction of Apoptosis; Laboratories; Malignant - descriptor; Malignant Neoplasms; Mediating; Membrane Fusion; Mesenchymal Stem Cells; Modeling; Natural Immunity; Normal Cell; Oncolytic; Oncolytic viruses; Outcome; Pathway interactions; Patients; Pharmaceutical Preparations; Phase; Play; Preclinical Testing; Property; Proteins; Ras Signaling Pathway; Resistance; Role; Route; Simplexvirus; Staging; Testing; Therapeutic; Toxic effect; Toxicology; Translating; Treatment Efficacy; Treatment Protocols; Tumor Tissue; Viral; Virus; Virus Diseases; Virus Replication; Work; base; cancer therapy; cell killing; chemotherapy; clinical application; design; gemcitabine; gene therapy; improved; in vivo; killings; mutant; neoplastic cell; novel; preclinical study; public health relevance; ras GTPase-Activating Proteins; success; trafficking; tumor

DESCRIPTION (provided by applicant): Oncolytic viruses have proved safe and effective in preclinical testing and are now in clinical trials for patients with a variety of malignant diseases. The current generation of oncolytic herpes simplex viruses (HSVs) was constructed exclusively from type 1 virus (HSV-1) and their tumor selectivity was largely achieved by targeting dividing cells. We recently constructed a novel oncolytic virus from HSV-2 that can selectively replicate in and lyse tumor cells with an activated Ras signaling pathway. Designated FusOn-H2, the mutant virus features multiple antitumor mechanisms, including the induction of cell membrane fusion (syncytia formation) and apoptosis in tumor cells, and thus has potent antitumor activity when tested in different tumor models. Nonetheless, we are well aware of the remaining barriers to successful clinical application of FusOn-H2-mediated virotherapy. For example, the antitumor effect of any oncolytic virus is greatly diminished by the host's innate immunity, which can be instantly activated during virus infection, leading us to suggest that interference with key components of the innate immune system might enhance the oncolytic effects of FusOn-H2. We also hypothesize that the unique oncolytic mechanisms of FusOn- H2 could be exploited in combination regimens with chemotherapy to further potentiate the tumor cell destruction, and that mesenchymal stem cells would function as ideal cell carriers to selectively and repeatedly deliver the oncolytic virus to tumor tissues, even in the presence of active antiviral immunity. We have proposed three specific aims to test these predictions both in vitro and in vivo, with the long-term goal of developing a potent and safe virotherapy that could be translated into a clinically useful strategy in the near future. Successful outcomes of these preclinical studies will have significant implications for the design of future clinical trials of this novel oncolytic virus, as one or more of these enhancement strategies may be implemented to potentiate this virotherapy. PUBLIC HEALTH RELEVANCE: Using viruses to kill tumor cells has shown considerable promise in the laboratory and in early clinical trials. Yet several obstacles must be overcome before this strategy gains acceptance as a safe and potent form of cancer therapy. The applicant has constructed a virus from herpes simplex virus type 2, called FusOn-H2, which has produced encouraging antitumor activity in animal tumor models. He now proposes to develop and test different strategies for improving FusOn-H2 virotherapy, with the long-term goal of translating this treatment into a clinically feasible option for patients with malignant sold tumors.

描述（申请人提供）：溶瘤病毒在临床前测试中已被证明是安全有效的，目前正处于针对多种恶性疾病患者的临床试验中。当前一代的溶瘤单纯疱疹病毒 (HSV) 完全由 1 型病毒 (HSV-1) 构建，其肿瘤选择性很大程度上是通过靶向分裂细胞来实现的。我们最近从 HSV-2 构建了一种新型溶瘤病毒，它可以通过激活的 Ras 信号通路选择性地在肿瘤细胞中复制并裂解肿瘤细胞。这种突变病毒被命名为FusOn-H2，具有多种抗肿瘤机制，包括诱导细胞膜融合（合胞体形成）和肿瘤细胞凋亡，因此在不同肿瘤模型中测试时具有有效的抗肿瘤活性。尽管如此，我们很清楚 FusOn-H2 介导的病毒疗法在临床上成功应用仍然存在障碍。例如，任何溶瘤病毒的抗肿瘤作用都会因宿主的先天免疫而大大减弱，而宿主的先天免疫可以在病毒感染期间立即激活，这使我们认为干扰先天免疫​​系统的关键组成部分可能会增强FusOn-的溶瘤作用H2。我们还假设 FusOn-H2 独特的溶瘤机制可以与化疗联合使用，以进一步增强肿瘤细胞的破坏，并且间充质干细胞将作为理想的细胞载体，选择性地、重复地将溶瘤病毒递送至肿瘤组织，即使存在主动抗病毒免疫。我们提出了三个具体目标来在体外和体内测试这些预测，长期目标是开发一种有效且安全的病毒疗法，在不久的将来可以转化为临床上有用的策略。这些临床前研究的成功结果将对这种新型溶瘤病毒未来临床试验的设计产生重大影响，因为可以实施一种或多种增强策略来增强这种病毒疗法。公共卫生相关性：使用病毒杀死肿瘤细胞在实验室和早期临床试验中已显示出巨大的前景。然而，在这种策略被接受为安全有效的癌症治疗形式之前，必须克服一些障碍。申请人已经从2型单纯疱疹病毒构建了一种病毒，称为FusOn-H2，该病毒在动物肿瘤模型中产生了令人鼓舞的抗肿瘤活性。他现在提议开发和测试不同的策略来改进 FusOn-H2 病毒疗法，长期目标是将这种疗法转化为恶性肿瘤患者的临床可行选择。