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肿瘤溶瘤病毒诱导的抗肿瘤免疫的药物调节。

Pharmacological modulation of anti-tumor immunity induced by oncolytic viruses.

机构信息

Center for Innovative Cancer Research, Ottawa Hospital Research Institute , Ottawa, ON , Canada ; Faculty of Medicine, University of Ottawa , Ottawa, ON , Canada.

出版信息

Front Oncol. 2014 Jul 23;4:191. doi: 10.3389/fonc.2014.00191. eCollection 2014.

DOI:10.3389/fonc.2014.00191
PMID:25101247
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4108035/
Abstract

Oncolytic viruses (OVs) not only kill cancer cells by direct lysis but also generate a significant anti-tumor immune response that allows for prolonged cancer control and in some cases cures. How to best stimulate this effect is a subject of intense investigation in the OV field. While pharmacological manipulation of the cellular innate anti-viral immune response has been shown by several groups to improve viral oncolysis and spread, it is increasingly clear that pharmacological agents can also impact the anti-tumor immune response generated by OVs and related tumor vaccination strategies. This review covers recent progress in using pharmacological agents to improve the activity of OVs and their ability to generate robust anti-tumor immune responses.

摘要

溶瘤病毒 (OVs) 不仅可以通过直接裂解杀死癌细胞,还可以产生显著的抗肿瘤免疫反应,从而实现对癌症的长期控制,甚至在某些情况下可以治愈癌症。如何最好地刺激这种效应是 OV 领域中一个研究热点。虽然已有多个研究小组证明,通过药理学手段来调节细胞固有抗病毒免疫反应,可以提高病毒的溶瘤作用和传播能力,但越来越明显的是,药理学药物也会影响 OV 产生的抗肿瘤免疫反应以及相关的肿瘤疫苗策略。本文综述了近年来利用药理学手段来提高 OV 的活性及其产生强大抗肿瘤免疫反应的能力的最新进展。

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本文引用的文献

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Combining oncolytic HSV-1 with immunogenic cell death-inducing drug mitoxantrone breaks cancer immune tolerance and improves therapeutic efficacy.联合溶瘤单纯疱疹病毒 1 和免疫原性细胞死亡诱导药物米托蒽醌打破癌症免疫耐受并提高治疗效果。
Cancer Immunol Res. 2013 Nov;1(5):309-19. doi: 10.1158/2326-6066.CIR-13-0059-T. Epub 2013 Aug 19.
2
Localized oncolytic virotherapy overcomes systemic tumor resistance to immune checkpoint blockade immunotherapy.局部溶瘤病毒治疗克服了系统肿瘤对免疫检查点阻断免疫治疗的耐药性。
Sci Transl Med. 2014 Mar 5;6(226):226ra32. doi: 10.1126/scitranslmed.3008095.
3
Complementary induction of immunogenic cell death by oncolytic parvovirus H-1PV and gemcitabine in pancreatic cancer.溶瘤细小病毒 H-1PV 和吉西他滨协同诱导胰腺癌免疫原性细胞死亡。
J Virol. 2014 May;88(10):5263-76. doi: 10.1128/JVI.03688-13. Epub 2014 Feb 26.
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PI3K inhibitor LY294002 inhibits activation of the Akt/mTOR pathway induced by an oncolytic adenovirus expressing TRAIL and sensitizes multiple myeloma cells to the oncolytic virus.磷脂酰肌醇-3激酶(PI3K)抑制剂LY294002可抑制表达肿瘤坏死因子相关凋亡诱导配体(TRAIL)的溶瘤腺病毒所诱导的Akt/mTOR信号通路的激活,并使多发性骨髓瘤细胞对该溶瘤病毒敏感。
Oncol Rep. 2014 Apr;31(4):1581-8. doi: 10.3892/or.2014.3020. Epub 2014 Feb 11.
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Exploiting tumor epigenetics to improve oncolytic virotherapy.利用肿瘤表观遗传学提高溶瘤病毒治疗效果。
Front Genet. 2013 Sep 20;4:184. doi: 10.3389/fgene.2013.00184.