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[溶瘤性柯萨奇病毒疗法作为一种免疫刺激剂]

[Oncolytic coxsackievirus therapy as an immunostimulator].

作者信息

Miyamoto Shohei, Sagara Miyako, Kohara Hiroshi, Tani Kenzaburo

机构信息

Project Division of ALA Advanced Medical Research, The Institute of Medical Science, The University of Tokyo.

出版信息

Rinsho Ketsueki. 2017;58(8):977-982. doi: 10.11406/rinketsu.58.977.

Abstract

Recently, the active development of oncolytic virotherapy has gathered attention. Enterovirus research seeks to better understand its pathogenicity. In particular, coxsackievirus A21 (CVA21) is a promising candidate for oncolytic virotherapy, and thus is the focus of many clinical trials. We have reported that coxsackievirus B3 (CVB3) had potent oncolytic activity for cancer, and induced immunogenic cell death of CVB3-infected cells. We then genetically engineered wild type CVB3 and successfully produced a novel recombinant CVB3-miRT, improving its safety by the introducing an organ-specific miRNA target sequence. We also developed the production method of CVB3 agent, and are conducting a clinical trial of CVB3 therapy for cancer patients. In this report, we review recent clinical progress in oncolytic virotherapy of CVA21 and clinical development of our CVB3.

摘要

最近,溶瘤病毒疗法的积极发展引起了关注。肠道病毒研究旨在更好地了解其致病性。特别是,柯萨奇病毒A21(CVA21)是溶瘤病毒疗法的一个有前景的候选者,因此是许多临床试验的重点。我们已经报道柯萨奇病毒B3(CVB3)对癌症具有强大的溶瘤活性,并诱导CVB3感染细胞发生免疫原性细胞死亡。然后,我们对野生型CVB3进行基因工程改造,成功生产出一种新型重组CVB3-miRT,通过引入器官特异性miRNA靶序列提高了其安全性。我们还开发了CVB3制剂的生产方法,并正在对癌症患者进行CVB3治疗的临床试验。在本报告中,我们综述了CVA21溶瘤病毒疗法的近期临床进展以及我们的CVB3的临床开发情况。

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