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免疫原性肿瘤细胞死亡、溶瘤病毒与免疫系统的关键相互作用决定了联合免疫疗法的合理设计。

Critical Interactions between Immunogenic Cancer Cell Death, Oncolytic Viruses, and the Immune System Define the Rational Design of Combination Immunotherapies.

机构信息

Department of Pathobiology, Ontario Veterinary College, University of Guelph, Guelph, Ontario N1G 2W1, Canada.

Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario L8S 4L8, Canada.

出版信息

J Immunol. 2018 Jan 15;200(2):450-458. doi: 10.4049/jimmunol.1701021.

Abstract

Oncolytic viruses (OVs) are multimodal cancer therapeutics, with one of their dominant mechanisms being in situ vaccination. There is a growing consensus that optimal cancer therapies should generate robust tumor-specific immune responses. Immunogenic cell death (ICD) is a paradigm of cellular demise culminating in the spatiotemporal release of danger-associated molecular patterns that induce potent anticancer immunity. Alongside traditional ICD inducers like anthracycline chemotherapeutics and radiation, OVs have emerged as novel members of this class of therapeutics. OVs replicate in cancers and release tumor Ags, which are perceived as dangerous because of simultaneous expression of pathogen-associated molecular patterns that activate APCs. Therefore, OVs provide the target Ags and danger signals required to induce adaptive immune responses. This review discusses why OVs are attractive candidates for generating ICD, biological barriers limiting their success in the clinic, and groundbreaking strategies to potentiate ICD and antitumor immunity with rationally designed OV-based combination therapies.

摘要

溶瘤病毒(OVs)是一种多模式的癌症治疗方法,其主要机制之一是原位疫苗接种。越来越多的共识认为,最佳的癌症治疗方法应该产生强大的肿瘤特异性免疫反应。免疫原性细胞死亡(ICD)是细胞死亡的典范,最终导致危险相关分子模式的时空释放,从而诱导强烈的抗癌免疫。除了蒽环类化疗药物和放疗等传统 ICD 诱导剂外,OVs 也成为该类治疗药物的新成员。OVs 在癌症中复制并释放肿瘤 Ag,由于同时表达激活 APC 的病原体相关分子模式,这些 Ag 被视为危险。因此,OVs 提供了诱导适应性免疫反应所需的靶 Ag 和危险信号。这篇综述讨论了为什么 OVs 是产生 ICD 的有吸引力的候选者,限制它们在临床上成功的生物学障碍,以及通过合理设计基于 OV 的联合治疗来增强 ICD 和抗肿瘤免疫的开创性策略。

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