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基于水疱性口炎病毒的溶瘤病毒疗法的最新进展:五年回顾

Recent advances in vesicular stomatitis virus-based oncolytic virotherapy: a 5-year update.

作者信息

Felt Sébastien A, Grdzelishvili Valery Z

机构信息

Department of Biological Sciences, University of North Carolina at Charlotte, Charlotte, NC, USA.

出版信息

J Gen Virol. 2017 Dec;98(12):2895-2911. doi: 10.1099/jgv.0.000980.

Abstract

Oncolytic virus (OV) therapy is an anti-cancer approach that uses viruses that preferentially infect, replicate in and kill cancer cells. Vesicular stomatitis virus (VSV, a rhabdovirus) is an OV that is currently being tested in the USA in several phase I clinical trials against different malignancies. Several factors make VSV a promising OV: lack of pre-existing human immunity against VSV, a small and easy to manipulate genome, cytoplasmic replication without risk of host cell transformation, independence of cell cycle and rapid growth to high titres in a broad range of cell lines facilitating large-scale virus production. While significant advances have been made in VSV-based OV therapy, room for improvement remains. Here we review recent studies (published in the last 5 years) that address 'old' and 'new' challenges of VSV-based OV therapy. These studies focused on improving VSV safety, oncoselectivity and oncotoxicity; breaking resistance of some cancers to VSV; preventing premature clearance of VSV; and stimulating tumour-specific immunity. Many of these approaches were based on combining VSV with other therapeutics. This review also discusses another rhabdovirus closely related to VSV, Maraba virus, which is currently being tested in Canada in phase I/II clinical trials.

摘要

溶瘤病毒(OV)疗法是一种抗癌方法,它使用的病毒能够优先感染癌细胞、在癌细胞中复制并杀死癌细胞。水泡性口炎病毒(VSV,一种弹状病毒)是一种溶瘤病毒,目前正在美国进行多项针对不同恶性肿瘤的I期临床试验。有几个因素使VSV成为一种有前景的溶瘤病毒:人类对VSV不存在预先存在的免疫力、基因组小且易于操作、在细胞质中复制且无宿主细胞转化风险、不依赖细胞周期且能在多种细胞系中快速生长至高滴度,便于大规模生产病毒。虽然基于VSV的溶瘤病毒疗法已取得显著进展,但仍有改进空间。在此,我们综述了最近(过去5年发表)针对基于VSV的溶瘤病毒疗法的“旧”挑战和“新”挑战的研究。这些研究聚焦于提高VSV的安全性、肿瘤选择性和肿瘤毒性;打破某些癌症对VSV的抗性;防止VSV过早清除;以及刺激肿瘤特异性免疫。其中许多方法基于将VSV与其他疗法相结合。本综述还讨论了另一种与VSV密切相关的弹状病毒——马拉巴病毒,它目前正在加拿大进行I/II期临床试验。

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本文引用的文献

2
Oncolytic VSV Primes Differential Responses to Immuno-oncology Therapy.
Mol Ther. 2017 Aug 2;25(8):1917-1932. doi: 10.1016/j.ymthe.2017.05.006. Epub 2017 Jun 2.
3
Oncolytic Maraba Virus MG1 as a Treatment for Sarcoma.
Int J Cancer. 2017 Sep 15;141(6):1257-1264. doi: 10.1002/ijc.30813. Epub 2017 Jun 21.
5
Activation of Nrf2 Signaling Augments Vesicular Stomatitis Virus Oncolysis via Autophagy-Driven Suppression of Antiviral Immunity.
Mol Ther. 2017 Aug 2;25(8):1900-1916. doi: 10.1016/j.ymthe.2017.04.022. Epub 2017 May 17.
7
Combining Oncolytic Virotherapy with p53 Tumor Suppressor Gene Therapy.
Mol Ther Oncolytics. 2017 Mar 21;5:20-40. doi: 10.1016/j.omto.2017.03.002. eCollection 2017 Jun 16.
8
Oncolytic Virotherapy: A Contest between Apples and Oranges.
Mol Ther. 2017 May 3;25(5):1107-1116. doi: 10.1016/j.ymthe.2017.03.026. Epub 2017 Apr 6.
9
Inhibitory Receptors Induced by VSV Viroimmunotherapy Are Not Necessarily Targets for Improving Treatment Efficacy.
Mol Ther. 2017 Apr 5;25(4):962-975. doi: 10.1016/j.ymthe.2017.01.023. Epub 2017 Feb 22.
10
NK-Cell Recruitment Is Necessary for Eradication of Peritoneal Carcinomatosis with an IL12-Expressing Maraba Virus Cellular Vaccine.
Cancer Immunol Res. 2017 Mar;5(3):211-221. doi: 10.1158/2326-6066.CIR-16-0162. Epub 2017 Feb 3.

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