School of Life Sciences, University of Warwick, Coventry CV4 7AL, UK.
Vaccine. 2011 Mar 24;29(15):2777-84. doi: 10.1016/j.vaccine.2011.01.102. Epub 2011 Feb 12.
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.
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。