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教程:用于癌症免疫疗法的溶瘤病毒的设计、生产和测试。

Tutorial: design, production and testing of oncolytic viruses for cancer immunotherapy.

机构信息

Department of Pathology, Dalhousie University, Halifax, Nova Scotia, Canada.

Department of Microbiology and Immunology, Dalhousie University, Halifax, Nova Scotia, Canada.

出版信息

Nat Protoc. 2024 Sep;19(9):2540-2570. doi: 10.1038/s41596-024-00985-1. Epub 2024 May 20.

Abstract

Oncolytic viruses (OVs) represent a novel class of cancer immunotherapy agents that preferentially infect and kill cancer cells and promote protective antitumor immunity. Furthermore, OVs can be used in combination with established or upcoming immunotherapeutic agents, especially immune checkpoint inhibitors, to efficiently target a wide range of malignancies. The development of OV-based therapy involves three major steps before clinical evaluation: design, production and preclinical testing. OVs can be designed as natural or engineered strains and subsequently selected for their ability to kill a broad spectrum of cancer cells rather than normal, healthy cells. OV selection is further influenced by multiple factors, such as the availability of a specific viral platform, cancer cell permissivity, the need for genetic engineering to render the virus non-pathogenic and/or more effective and logistical considerations around the use of OVs within the laboratory or clinical setting. Selected OVs are then produced and tested for their anticancer potential by using syngeneic, xenograft or humanized preclinical models wherein immunocompromised and immunocompetent setups are used to elucidate their direct oncolytic ability as well as indirect immunotherapeutic potential in vivo. Finally, OVs demonstrating the desired anticancer potential progress toward translation in patients with cancer. This tutorial provides guidelines for the design, production and preclinical testing of OVs, emphasizing considerations specific to OV technology that determine their clinical utility as cancer immunotherapy agents.

摘要

溶瘤病毒 (OVs) 代表了一类新型的癌症免疫治疗药物,它们能够优先感染和杀死癌细胞,并促进保护性抗肿瘤免疫。此外,OVs 可以与现有的或即将出现的免疫治疗药物联合使用,特别是免疫检查点抑制剂,从而有效地针对广泛的恶性肿瘤。在进行临床评估之前,基于 OV 的治疗的发展涉及三个主要步骤:设计、生产和临床前测试。OVs 可以设计为天然或工程菌株,然后根据其杀死广谱癌细胞而不是正常健康细胞的能力进行选择。OV 选择还受到多种因素的影响,例如特定病毒平台的可用性、癌细胞的易感性、需要进行基因工程以使病毒无毒和/或更有效,以及在实验室或临床环境中使用 OV 的后勤考虑因素。选定的 OVs 然后通过使用同基因、异种移植或人源化的临床前模型进行生产和测试,以评估其抗癌潜力,其中免疫缺陷和免疫功能正常的设置用于阐明其直接溶瘤能力以及体内的间接免疫治疗潜力。最后,表现出所需抗癌潜力的 OVs 会在癌症患者中进行转化研究。本教程提供了设计、生产和临床前测试 OVs 的指南,强调了决定其作为癌症免疫治疗药物的临床应用的 OV 技术的具体考虑因素。

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