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一种新型广谱呼吸道病毒感染治疗方法:基于流感的缺陷型干扰病毒可提供针对呼吸道合胞病毒感染的体内保护。

A novel broad-spectrum treatment for respiratory virus infections: influenza-based defective interfering virus provides protection against pneumovirus infection in vivo.

机构信息

School of Life Sciences, University of Warwick, Coventry CV4 7AL, UK.

出版信息

Vaccine. 2011 Mar 24;29(15):2777-84. doi: 10.1016/j.vaccine.2011.01.102. Epub 2011 Feb 12.

DOI:10.1016/j.vaccine.2011.01.102
PMID:21320545
Abstract

Respiratory viruses represent a major clinical burden. Few vaccines and antivirals are available, and the rapid appearance of resistant viruses is a cause for concern. We have developed a novel approach which exploits defective viruses (defective interfering (DI) or protecting viruses). These are naturally occurring deletion mutants which are replication-deficient and multiply only when coinfection with a genetically compatible infectious virus provides missing function(s) in trans. Interference/protection is believed to result primarily from genome competition and is therefore usually confined to the virus from which the DI genome originated. Using intranasally administered protecting influenza A virus we have successfully protected mice from lethal in vivo infection with influenza A viruses from several different subtypes [1]. Here we report, contrary to expectation, that protecting influenza A virus also protects in vivo against a genetically unrelated respiratory virus, pneumonia virus of mice, a pneumovirus from the family Paramyxoviridae. A single dose that contains 1μg of protecting virus protected against lethal infection. This protection is achieved by stimulating type I interferon and possibly other elements of innate immunity. Protecting virus thus has the potential to protect against all interferon-sensitive respiratory viruses and all influenza A viruses.

摘要

呼吸道病毒是一个主要的临床负担。目前可用的疫苗和抗病毒药物很少,而耐药病毒的迅速出现令人担忧。我们开发了一种新的方法,利用缺陷病毒(缺陷干扰(DI)或保护病毒)。这些是自然发生的缺失突变体,其复制缺陷,只有在与遗传上相容的传染性病毒共同感染时,才能提供转位缺失的功能。干扰/保护主要被认为是由于基因组竞争所致,因此通常仅限于 DI 基因组来源的病毒。我们使用鼻内给予的保护型流感 A 病毒,成功地保护了小鼠免受来自几种不同亚型的流感 A 病毒的体内致死性感染[1]。在这里,我们报告了一个出乎意料的结果,即保护型流感 A 病毒也能在体内保护免受遗传上不相关的呼吸道病毒,即鼠肺炎病毒,这是副粘病毒科的一种肺炎病毒。含有 1μg 保护病毒的单剂量即可预防致死性感染。这种保护是通过刺激 I 型干扰素和可能的其他先天免疫元件实现的。因此,保护病毒有可能预防所有干扰素敏感的呼吸道病毒和所有流感 A 病毒。

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