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聚合物涂层病毒载体:用于基因治疗的杂交纳米系统。

Polymer-coated viral vectors: hybrid nanosystems for gene therapy.

机构信息

Centre for Nanotechnology & Advanced Biomaterials (CeNTAB), SASTRA Deemed-to-be University, Thanjavur, India.

Department of Biological Sciences and Bioengineering, Indian Institute of Technology, Kanpur, Uttar Pradesh, India.

出版信息

J Gene Med. 2018 Apr;20(4):e3011. doi: 10.1002/jgm.3011. Epub 2018 Mar 25.

Abstract

The advantages and critical aspects of nanodimensional polymer-coated viral vector systems potentially applicable for gene delivery are reviewed. Various viral and nonviral vectors have been explored for gene therapy. Viral gene transfer methods, although highly efficient, are limited by their immunogenicity. Nonviral vectors have a lower transfection efficiency as a result of their inability to escape from the endosome. To overcome these drawbacks, novel nanotechnology-mediated interventions that involve the coating or modification of virus using polymers have emerged as a new paradigm in gene therapy. These alterations not only modify the tropism of the virus, but also reduce their undesirable interactions with the biological system. Also, co-encapsulation of other therapeutic agents in the polymeric coating may serve to augment the treatment efficacy. The viral particles can aid endosomal escape, as well as nuclear targeting, thereby enhancing the transfection efficiency. The integration of the desirable properties of both viral and nonviral vectors has been found beneficial for gene therapy by enhancing the transduction efficiency and minimizing the immune response. However, it is essential to ensure that these attempts should not compromise on the inherent ability of viruses to target and internalize into the cells and escape the endosomes.

摘要

本文综述了纳米级聚合物涂层病毒载体系统在基因传递方面的优势和关键方面。已经探索了各种病毒和非病毒载体用于基因治疗。病毒基因转移方法虽然效率很高,但由于其免疫原性而受到限制。非病毒载体由于不能从内涵体逃逸,因此转染效率较低。为了克服这些缺点,新型纳米技术介导的干预措施已经出现,涉及使用聚合物对病毒进行涂层或修饰,这是基因治疗的一个新范例。这些改变不仅改变了病毒的嗜性,还减少了它们与生物系统的不良相互作用。此外,将其他治疗剂共同包封在聚合物涂层中可能有助于增强治疗效果。病毒颗粒可以帮助内涵体逃逸和核靶向,从而提高转染效率。通过提高转导效率和最小化免疫反应,整合病毒和非病毒载体的理想特性已被发现有益于基因治疗。然而,至关重要的是,这些尝试不应损害病毒靶向和内化细胞以及逃避内涵体的固有能力。

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