Creation of Immuno-Oncolytic Viruses for Cancer Therapy

创造用于癌症治疗的免疫溶瘤病毒

• 批准号: 8693175
• 负责人: Stephen H Thorne
• 金额: $ 31.9万
• 依托单位: UNIVERSITY OF PITTSBURGH AT PITTSBURGH
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-05-01 至 2019-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8693175
• 关键词: Affect; Animal Model; Antibodies; Antigens; Area; Autoantigens; Cell Cycle Regulation; Cells; Clinic; Clinical; Clinical Trials; Data; Development; ERBB2 gene; Engineering; Equilibrium; Funding; Gene Deletion; Genes; Goals; Granulocyte-Macrophage Colony-Stimulating Factor; Growth Factor Gene; Human; Immune; Immune Targeting; Immune response; Immune system; Immunity; Immunocompetent; Immunosuppression; Immunotherapeutic agent; In Situ; In Vitro; Intravenous; Kinetics; Malignant Neoplasms; Mediating; Modeling; Modification; Mus; Neoplasm Metastasis; Oncolytic; Oncolytic viruses; Pathway interactions; Patients; Phase; Phase I Clinical Trials; Population; Pre-Clinical Model; Primary Neoplasm; Production; Relapse; Reporting; Residual Tumors; Role; Safety; Signal Pathway; Signal Transduction; Specimen; TK Gene; Technology; Testing; Therapeutic; Therapeutic Effect; Thymidine Kinase; Time; Treatment Protocols; Tumor Antigens; Tumor Immunity; Vaccination; Vaccine Therapy; Vaccines; Vaccinia; Vaccinia virus; Vaccinium; Vertebral column; Viral; Viral Antigens; Viral Genome; Viral Vector; Virulence; Virus; Virus Diseases; Virus Replication; Weight; Work; adaptive immunity; aldehyde dehydrogenase 1; aldehyde dehydrogenases; arm; base; cancer cell; cancer therapy; cytokine; design; immunogenicity; in vitro testing; in vivo; interest; killings; mouse model; neoplastic cell; neutralizing antibody; next generation; novel; novel therapeutics; oncolysis; oncolytic vector; particle; pre-clinical; prevent; public health relevance; randomized trial; research clinical testing; therapeutic vaccine; tumor; vector

DESCRIPTION (provided by applicant): There has been a recent and justified resurgence in interest in the use of oncolytic viruses for cancer therapy, primarily due to highly promising Phase II data with at least three different viral strains and recent early Phase III data. It is noteworthy that multiple vectors currently undergoing randomized trials express a cytokine to enhance their therapeutic effects, and have been reported to induce anti-tumor immunity. However, the immunotherapeutic potential of this platform remains under-developed. We have demonstrated both in pre-clinical models and in the clinic that oncolytic vaccinia can raise protective immunity against tumor antigens. Indeed, under some circumstances oncolytic vaccinia provides potent anti-tumor effects entirely through immunotherapeutic mechanisms of action. However, while the powerful immunogenicity of vaccinia is appreciated and relatively well understood from its use as a vaccine, the current oncolytic strains have not been designed to take advantage of this potential. We therefore propose to develop next generation vectors that act as potent and specific immunotherapeutics. Importantly we will look to do this without deleteriously affecting their directly oncolytic capabilities. It is believed that the logical desin of viral vectors to both replicate selectively in cancer cells and direct a specific and targeted immune response against the tumor will significantly enhance their therapeutic potential, and represents a novel treatment platform we have termed Immuno-Oncolytic Viruses (IOV). Optimization of immunotherapeutic effects will be achieved through inter-related approaches acting at a global level and at multiple steps in the immune response. Initially, we will incorporate technologies pioneered in the development of vaccine therapies to selectively modulate TLR activation and the innate immune response and apply these to oncolytic vaccinia. By re-directing, rather than simply activating innate immune pathways it is possible to modulate the overall immune response without deleteriously affecting viral oncolytic activity. Secondly, we will manipulate immune-modulatory virulence genes encoded by vaccinia in order to re-direct the naturally Th2-weighted immune response raised by vaccinia towards the potentially more beneficial Th1 arm. Finally, the expression of specific antigens will be used to boost the immune targeting of the bulk tumor and of specific subsets of cells within the tumor, notably tumor initiating cells. The vectors produced in this work will become next generation therapeutics with predefined immunotherapeutic mechanisms of action and significantly enhanced anti-tumor effects. They will undergo (independently funded) GMP manufacture over the same time frame as this work and so be ready for immediate clinical testing by the completion of this study and incorporating treatment regimens developed within this application.

描述(由申请人提供)：最近，人们对使用溶瘤病毒进行癌症治疗的兴趣重新燃起，这是合理的，主要是由于具有至少三种不同病毒株的非常有希望的第二阶段数据和最近的第三阶段早期数据。值得注意的是，目前正在进行随机试验的多个载体表达一种细胞因子以增强其治疗效果，并已被报道可诱导抗肿瘤免疫。然而，该平台的免疫治疗潜力仍未得到充分开发。我们已经在临床前模型和临床上证明了溶瘤疫苗可以提高对肿瘤抗原的保护性免疫。事实上，在某些情况下，溶瘤疫苗完全通过免疫治疗的作用机制提供了强大的抗肿瘤效果。然而，虽然人们从牛痘作为疫苗的使用中认识到并相对较好地了解了牛痘的强大免疫原性，但目前的溶瘤菌株并未被设计为利用这一潜力。因此，我们建议开发下一代载体，作为有效和特异的免疫疗法。重要的是，我们将寻求在不直接影响他们的溶瘤能力的情况下做到这一点。人们认为，合理地设计病毒载体既能在肿瘤细胞中选择性复制，又能针对肿瘤产生特异性和靶向性的免疫反应，将显著增强其治疗潜力，并代表了一种新的治疗平台，我们称之为免疫溶瘤病毒(IOV)。免疫治疗效果的优化将通过在全球一级和在免疫反应的多个步骤中采取相互关联的方法来实现。最初，我们将整合在疫苗疗法开发中首创的技术，以选择性地调节TLR激活和先天免疫反应，并将这些技术应用于溶瘤疫苗。通过改变方向，而不是简单地激活先天免疫途径，有可能在不有害地影响病毒溶瘤活性的情况下调节整体免疫反应。其次，我们将操纵牛痘病毒编码的免疫调节毒力基因，以便将牛痘病毒自然产生的Th2加权免疫反应重新定向到潜在更有益的Th1臂。最后，特定抗原的表达将被用来增强对实体肿瘤和肿瘤内特定细胞亚群的免疫靶向性，特别是肿瘤起始细胞。在这项工作中产生的载体将成为具有预先确定的免疫治疗作用机制并显著增强抗肿瘤效果的下一代疗法。他们将在与这项工作相同的时间框架内进行(独立资助的)GMP生产，因此在完成这项研究并纳入在这项应用中开发的治疗方案后，可以立即进行临床测试。