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单纯疱疹病毒作为疫苗开发和基因治疗的载体。

HSV as a vector in vaccine development and gene therapy.

机构信息

Department of Experimental and Diagnostic Medicine-Section of Microbiology, University of Ferrara, Via Luigi Borsari 46, Ferrara, 44100, Italy.

出版信息

Adv Exp Med Biol. 2009;655:118-44. doi: 10.1007/978-1-4419-1132-2_10.

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)的遗传学和分子生物学方面的深入研究,为人类病原体的研究提供了重要的基础。HSV 的生活方式基于与受感染宿主的长期双重相互作用,其特征是存在裂解和潜伏感染。这为多种人类医疗保健应用中的潜在载体的发展提供了可能性。这些载体包括将人类基因递送到神经系统细胞中、选择性地破坏癌细胞、预防 HSV 或其他传染病的感染以及靶向感染特定的组织或器官。有三种不同类型的载体可以从 HSV-1 中衍生出来:复制能力减弱的载体、复制能力丧失的重组载体和称为扩增子的缺陷辅助依赖性载体。本章重点介绍了设计、构建和最近应用方面的最新知识,以及三种不同类型的 HSV-1 载体的潜力和当前限制。

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