Immune cells: more than simple carriers for systemic delivery of oncolytic viruses.

IF 6.7 Oncolytic Virotherapy Pub Date : 2014-01-01 DOI:10.2147/OV.S47143
Samuel Eisenstein, Shu-Hsia Chen, Ping-Ying Pan
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引用次数: 9

Abstract

Oncolytic virotherapy on its own has numerous drawbacks, including an inability of the virus to actively target tumor cells and systemic toxicities at the high doses necessary to effectively treat tumors. Addition of immune cell-based carriers of oncolytic viruses holds promise as a technique in which oncolytic virus can be delivered directly to tumors in smaller and less toxic doses. Interestingly, the cell carriers themselves have also demonstrated antitumor effects, which can be augmented further by tailoring the appropriate oncolytic virus to the appropriate cell type. This review discusses the multiple factors that go into devising an effective, cell-based delivery system for oncolytic viruses.

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免疫细胞:不仅仅是溶瘤病毒系统传递的简单载体。
溶瘤病毒疗法本身有许多缺点,包括病毒无法主动靶向肿瘤细胞,以及有效治疗肿瘤所需的高剂量全身性毒性。添加基于免疫细胞的溶瘤病毒载体是一种有希望的技术,在这种技术中,溶瘤病毒可以以更小和更低的毒性剂量直接递送到肿瘤。有趣的是,细胞载体本身也显示出抗肿瘤作用,这种作用可以通过将适当的溶瘤病毒定制为适当的细胞类型来进一步增强。这篇综述讨论了设计一种有效的、基于细胞的溶瘤病毒递送系统的多种因素。
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期刊最新文献
The Current State of Oncolytic Herpes Simplex Virus for Glioblastoma Treatment. Treatment of an Alveolar Rhabdomyosarcoma Allograft with Recombinant Myxoma Virus and Oclacitinib. Virus-Receptor Interactions and Virus Neutralization: Insights for Oncolytic Virus Development. Impact of Induced Syncytia Formation on the Oncolytic Potential of Myxoma Virus. Virus-Receptor Interactions: Structural Insights For Oncolytic Virus Development.
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