Power Anthony T, Bell John C
Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Centre for Cancer Therapeutics, Ottawa Health Research Institute, Ottawa Hospital, Ottawa, Ontario, Canada.
Mol Ther. 2007 Apr;15(4):660-5. doi: 10.1038/sj.mt.6300098. Epub 2007 Jan 30.
Recent years have seen tremendous advances in the development of exquisitely targeted replicating virotherapeutics that can safely destroy malignant cells. Despite this promise, clinical advancement of this powerful and unique approach has been hindered by vulnerability to host defenses and inefficient systemic delivery. However, it now appears that delivery of oncolytic viruses within carrier cells may offer one solution to this critical problem. In this review, we compare the advantages and limitations of the numerous cell lineages that have been investigated as delivery platforms for viral therapeutics, and discuss examples showing how combined cell-virus biotherapeutics can be used to achieve synergistic gains in antitumor activity. Finally, we highlight avenues for future preclinical research that might be taken in order to refine cell-virus biotherapeutics in preparation for human trials.
近年来,在能够安全摧毁恶性细胞的精准靶向复制性病毒疗法的开发方面取得了巨大进展。尽管有此前景,但这种强大而独特的方法在临床应用上却因易受宿主防御影响和全身递送效率低下而受阻。然而,现在看来,在载体细胞内递送溶瘤病毒可能为这一关键问题提供一种解决方案。在这篇综述中,我们比较了作为病毒疗法递送平台而被研究的众多细胞谱系的优缺点,并讨论了一些实例,展示了细胞 - 病毒联合生物疗法如何用于实现抗肿瘤活性的协同增效。最后,我们强调了未来临床前研究的方向,以便改进细胞 - 病毒生物疗法,为人体试验做准备。