超声介导的溶瘤病毒传递和摄取以提高治疗效果:最新进展。

IF 6.7
Oncolytic Virotherapy Pub Date : 2015-11-25 eCollection Date: 2015-01-01 DOI:10.2147/OV.S66097
Rounak Nande, Candace M Howard, Pier Paolo Claudio
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引用次数: 11

摘要

超声(US)领域已经从医学成像和诊断到治疗策略发生了重大变化。美国造影剂或微泡(MB)目前被用作化学药物、小分子、核酸、小干扰核糖核酸、蛋白质、腺病毒和溶瘤病毒的潜在载体。溶瘤病毒可以选择性地在癌细胞内复制并破坏癌细胞,从而使它们成为治疗晚期或转移性癌症的有力疗法。在临床试验中,将这些病毒直接注射到肿瘤结节中显示出强大的活性。然而,溶瘤病毒的有效性和其递送方式的局限性值得探索超声介导的递送。携带腺病毒或溶瘤病毒的基因治疗可与mb结合并静脉注射。在靶区应用US能量后,mb空化,产生的冲击波增强药物、基因或腺病毒的摄取。虽然潜在的机制尚未完全了解,但有证据表明,细胞膜的机械孔形成允许药物的暂时摄取。这种递送方法绕过了由于刺激免疫系统而阻止静脉注射病毒的限制。这篇综述提供了对溶瘤病毒向肿瘤部位递送这一有趣的新前沿的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ultrasound-mediated oncolytic virus delivery and uptake for increased therapeutic efficacy: state of art.

Ultrasound-mediated oncolytic virus delivery and uptake for increased therapeutic efficacy: state of art.

Ultrasound-mediated oncolytic virus delivery and uptake for increased therapeutic efficacy: state of art.

Ultrasound-mediated oncolytic virus delivery and uptake for increased therapeutic efficacy: state of art.

The field of ultrasound (US) has changed significantly from medical imaging and diagnosis to treatment strategies. US contrast agents or microbubbles (MB) are currently being used as potential carriers for chemodrugs, small molecules, nucleic acids, small interfering ribonucleic acid, proteins, adenoviruses, and oncolytic viruses. Oncolytic viruses can selectively replicate within and destroy a cancer cell, thus making them a powerful therapeutic in treating late-stage or metastatic cancer. These viruses have been shown to have robust activity in clinical trials when injected directly into tumor nodules. However limitations in oncolytic virus' effectiveness and its delivery approach have warranted exploration of ultrasound-mediated delivery. Gene therapy bearing adenoviruses or oncolytic viruses can be coupled with MBs and injected intravenously. Following application of US energy to the target region, the MBs cavitate, and the resulting shock wave enhances drug, gene, or adenovirus uptake. Though the underlying mechanism is yet to be fully understood, there is evidence to suggest that mechanical pore formation of cellular membranes allows for the temporary uptake of drugs. This delivery method circumvents the limitations due to stimulation of the immune system that prevented intravenous administration of viruses. This review provides insight into this intriguing new frontier on the delivery of oncolytic viruses to tumor sites.

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