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单纯疱疹病毒作为疫苗研发和基因治疗中的一种载体。

HSV as a vector in vaccine development and gene therapy.

作者信息

Marconi Peggy, Argnani Rafaela, Berto Elena, Epstein Alberto L, Manservigi Roberto

机构信息

Department of Experimental and Diagnostic Medicine, Section of Microbiology; University of Ferrara, Ferrara, Italy.

出版信息

Hum Vaccin. 2008 Mar-Apr;4(2):91-105. doi: 10.4161/hv.4.2.6212.

Abstract

The very deep knowledge acquired on the genetics and molecular biology of herpes simplex virus (HSV), major human pathogen whose lifestyle is based on a long-term dual interaction with the infected host characterized by the existence of lytic and latent infections, has allowed the development of potential vectors for several applications in human healthcare. These include delivery and expression of human genes to cells of the nervous system, selective destruction of cancer cells, prophylaxis against infection with HSV or other infectious diseases and targeted infection of specific tissues or organs. Three different classes of vectors can be derived from HSV-1: replication-competent attenuated vectors, replication-incompetent recombinant vectors and defective helper-dependent vectors known as amplicons. This chapter highlights the current knowledge concerning design, construction and recent applications, as well as the potential and current limitations of the three different classes of HSV-1-based vectors.

摘要

单纯疱疹病毒(HSV)是一种主要的人类病原体,其生活方式基于与受感染宿主的长期双重相互作用,其特征是存在裂解性感染和潜伏性感染。在HSV的遗传学和分子生物学方面所获得的深入知识,使得开发出了可用于人类医疗保健多种应用的潜在载体。这些应用包括将人类基因传递并表达至神经系统细胞、选择性破坏癌细胞、预防HSV感染或其他传染病以及对特定组织或器官进行靶向感染。三种不同类型的载体可源自HSV-1:具有复制能力的减毒载体、无复制能力的重组载体以及被称为扩增子的缺陷型辅助依赖载体。本章重点介绍了有关这三种不同类型的基于HSV-1的载体的设计、构建及近期应用的现有知识,以及它们的潜力和当前局限性。

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