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天然和重组肠道病毒的治疗用途。

Therapeutic Use of Native and Recombinant Enteroviruses.

作者信息

Ylä-Pelto Jani, Tripathi Lav, Susi Petri

机构信息

Department of Virology, University of Turku, Kiinamyllynkatu 13, 20520 Turku, Finland.

Biomaterials and Diagnostics Group, Turku University of Applied Sciences, 20520 Turku, Finland.

出版信息

Viruses. 2016 Feb 23;8(3):57. doi: 10.3390/v8030057.

Abstract

Research on human enteroviruses has resulted in the identification of more than 100 enterovirus types, which use more than 10 protein receptors and/or attachment factors required in cell binding and initiation of the replication cycle. Many of these "viral" receptors are overexpressed in cancer cells. Receptor binding and the ability to replicate in specific target cells define the tropism and pathogenesis of enterovirus types, because cellular infection often results in cytolytic response, i.e., disruption of the cells. Viral tropism and cytolytic properties thus make native enteroviruses prime candidates for oncolytic virotherapy. Copy DNA cloning and modification of enterovirus genomes have resulted in the generation of enterovirus vectors with properties that are useful in therapy or in vaccine trials where foreign antigenic epitopes are expressed from or on the surface of the vector virus. The small genome size and compact particle structure, however, set limits to enterovirus genome modifications. This review focuses on the therapeutic use of native and recombinant enteroviruses and the methods that have been applied to modify enterovirus genomes for therapy.

摘要

对人肠道病毒的研究已鉴定出100多种肠道病毒类型,它们利用10多种蛋白质受体和/或细胞结合及复制周期起始所需的附着因子。其中许多“病毒”受体在癌细胞中过度表达。受体结合以及在特定靶细胞中复制的能力决定了肠道病毒类型的嗜性和发病机制,因为细胞感染通常会导致细胞溶解反应,即细胞破裂。病毒嗜性和细胞溶解特性因此使天然肠道病毒成为溶瘤病毒疗法的主要候选对象。肠道病毒基因组的复制DNA克隆和修饰已产生了具有在治疗或疫苗试验中有用特性的肠道病毒载体,在这些试验中,外来抗原表位从载体病毒表达或在其表面表达。然而,小基因组大小和紧凑的颗粒结构对肠道病毒基因组修饰设置了限制。本综述重点关注天然和重组肠道病毒的治疗用途以及为治疗而应用于修饰肠道病毒基因组的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c656/4810247/c0035ea8d125/viruses-08-00057-g001.jpg

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