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本文引用的文献

1
Proteolytic disassembly is a critical determinant for reovirus oncolysis.蛋白水解拆解是呼肠孤病毒溶瘤作用的关键决定因素。
Mol Ther. 2007 Aug;15(8):1512-21. doi: 10.1038/sj.mt.6300207. Epub 2007 May 22.
2
Combined oncolytic and vaccination activities of parvovirus H-1 in a metastatic tumor model.细小病毒H-1在转移性肿瘤模型中的溶瘤与疫苗接种联合活性
Oncol Rep. 2007 Jun;17(6):1493-9.
3
Ras transformation mediates reovirus oncolysis by enhancing virus uncoating, particle infectivity, and apoptosis-dependent release.Ras转化通过增强病毒脱壳、颗粒感染性和凋亡依赖性释放来介导呼肠孤病毒的溶瘤作用。
Mol Ther. 2007 Aug;15(8):1522-30. doi: 10.1038/sj.mt.6300179. Epub 2007 Apr 24.
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Oncolytic viruses in cancer therapy.溶瘤病毒在癌症治疗中的应用
Cancer Lett. 2007 Sep 8;254(2):178-216. doi: 10.1016/j.canlet.2007.02.002. Epub 2007 Mar 23.
5
Oncolytic immunovirotherapy for melanoma using vesicular stomatitis virus.使用水疱性口炎病毒对黑色素瘤进行溶瘤免疫病毒疗法。
Cancer Res. 2007 Mar 15;67(6):2840-8. doi: 10.1158/0008-5472.CAN-06-3974.
6
History of oncolytic viruses: genesis to genetic engineering.溶瘤病毒的历史:起源到基因工程
Mol Ther. 2007 Apr;15(4):651-9. doi: 10.1038/sj.mt.6300108. Epub 2007 Feb 13.
7
An optimized clinical regimen for the oncolytic virus PV701.溶瘤病毒PV701的优化临床方案。
Clin Cancer Res. 2007 Feb 1;13(3):977-85. doi: 10.1158/1078-0432.CCR-06-1817.
8
Induction of strong antitumor immunity by an HSV-2-based oncolytic virus in a murine mammary tumor model.基于单纯疱疹病毒2型的溶瘤病毒在小鼠乳腺肿瘤模型中诱导强大的抗肿瘤免疫反应。
J Gene Med. 2007 Mar;9(3):161-9. doi: 10.1002/jgm.1005.
9
Incorporation of a laminin-derived peptide (SIKVAV) on polymer-modified adenovirus permits tumor-specific targeting via alpha6-integrins.在聚合物修饰的腺病毒上掺入层粘连蛋白衍生肽(SIKVAV)可通过α6整合素实现肿瘤特异性靶向。
Cancer Gene Ther. 2007 Apr;14(4):335-45. doi: 10.1038/sj.cgt.7701022. Epub 2007 Jan 19.
10
Systemic efficacy with oncolytic virus therapeutics: clinical proof-of-concept and future directions.溶瘤病毒疗法的全身疗效:临床概念验证及未来方向。
Cancer Res. 2007 Jan 15;67(2):429-32. doi: 10.1158/0008-5472.CAN-06-2871.

溶瘤病毒:它们在抗癌治疗中发挥作用吗?

Oncolytic viruses: do they have a role in anti-cancer therapy?

作者信息

Prestwich Robin J, Errington Fiona, Harrington Kevin J, Pandha Hardev S, Selby Peter, Melcher Alan

机构信息

Cancer Research UK, St James's University Hospital, Beckett Street, Leeds, LS9 7TF, UK.

出版信息

Clin Med Oncol. 2008;2:83-96. doi: 10.4137/cmo.s416. Epub 2008 Feb 9.

DOI:10.4137/cmo.s416
PMID:21892269
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3161683/
Abstract

Oncolytic viruses are replication competent, tumor selective and lyse cancer cells. Their potential for anti-cancer therapy is based upon the concept that selective intratumoral replication will produce a potent anti-tumor effect and possibly bystander or remote cell killing, whilst minimizing normal tissue toxicity. Viruses may be naturally oncolytic or be engineered for oncolytic activity, and possess a host of different mechanisms to provide tumor selectivity. Clinical use of live replicating viruses is associated with a unique set of safety issues. Clinical experience has so far provided evidence of limited efficacy and a favourable toxicity profile. The interaction with the host immune system is complex. An anti-viral immune response may limit efficacy by rapidly clearing the virus. However, virally-induced cell lysis releases tumor associated antigens in a 'dangerous' context, and limited evidence suggests that this can lead to the generation of a specific anti-tumor immune response. Combination therapy with chemotherapy or radiotherapy represents a promising avenue for ongoing translation of oncolytic viruses into clinical practice. Obstacles to therapy include highly effective non-specific host mechanisms to clear virus following systemic delivery, immune-mediated clearance, and intratumoral barriers limiting virus spread. A number of novel strategies are now under investigation to overcome these barriers. This review provides an overview of the potential role of oncolytic viruses, highlighting recent progress towards developing effective therapy and asks if they are a realistic therapeutic option at this stage.

摘要

溶瘤病毒具有复制能力、肿瘤选择性并能裂解癌细胞。它们用于抗癌治疗的潜力基于这样一种理念,即肿瘤内的选择性复制将产生强大的抗肿瘤作用,可能还会产生旁观者效应或远程杀伤细胞,同时将正常组织毒性降至最低。病毒可能天然具有溶瘤性,也可经工程改造获得溶瘤活性,并拥有一系列不同机制来实现肿瘤选择性。使用活的复制型病毒进行临床治疗会带来一系列独特的安全问题。目前的临床经验表明其疗效有限,但毒性特征良好。与宿主免疫系统的相互作用较为复杂。抗病毒免疫反应可能会通过快速清除病毒来限制疗效。然而,病毒诱导的细胞裂解在“危险”环境中释放肿瘤相关抗原,有限的证据表明这可能会导致产生特异性抗肿瘤免疫反应。与化疗或放疗联合治疗是将溶瘤病毒转化为临床实践的一个有前景的途径。治疗的障碍包括全身给药后清除病毒的高效非特异性宿主机制、免疫介导的清除以及限制病毒传播的肿瘤内屏障。目前正在研究一些新策略来克服这些障碍。本综述概述了溶瘤病毒的潜在作用,强调了在开发有效治疗方法方面的最新进展,并探讨了在现阶段它们是否是一种切实可行的治疗选择。