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Modifications in the Polymerase Genes of a Swine-Like Triple-Reassortant Influenza Virus To Generate Live Attenuated Vaccines against 2009 Pandemic H1N1 Viruses▿ †

机译:像猪的三重排列流感病毒聚合酶基因的修饰,以产生针对2009大流行H1N1病毒的减毒活疫苗▿†

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摘要

On 11 June 2009, the World Health Organization (WHO) declared that the outbreaks caused by novel swine-origin influenza A (H1N1) virus had reached pandemic proportions. The pandemic H1N1 (H1N1pdm) virus is the predominant influenza virus strain in the human population. It has also crossed the species barriers and infected turkeys and swine in several countries. Thus, the development of a vaccine that is effective in multiple animal species is urgently needed. We have previously demonstrated that the introduction of temperature-sensitive mutations into the PB2 and PB1 genes of an avian H9N2 virus, combined with the insertion of a hemagglutinin (HA) tag in PB1, resulted in an attenuated (att) vaccine backbone for both chickens and mice. Because the new pandemic strain is a triple-reassortant (TR) virus, we chose to introduce the double attenuating modifications into a swine-like TR virus isolate, A/turkey/OH/313053/04 (H3N2) (ty/04), with the goal of producing live attenuated influenza vaccines (LAIV). This genetically modified backbone had impaired polymerase activity and restricted virus growth at elevated temperatures. In vivo characterization of two H1N1 vaccine candidates generated using the ty/04 att backbone demonstrated that this vaccine is highly attenuated in mice, as indicated by the absence of signs of disease, limited replication, and minimum histopathological alterations in the respiratory tract. A single immunization with the ty/04 att-based vaccines conferred complete protection against a lethal H1N1pdm virus infection in mice. More importantly, vaccination of pigs with a ty/04 att-H1N1 vaccine candidate resulted in sterilizing immunity upon an aggressive intratracheal challenge with the 2009 H1N1 pandemic virus. Our studies highlight the safety of the ty/04 att vaccine platform and its potential as a master donor strain for the generation of live attenuated vaccines for humans and livestock.
机译:2009年6月11日,世界卫生组织(WHO)宣布,由新型猪源性甲型H1N1流感病毒引起的暴发已达到大流行程度。大流行的H1N1(H1N1pdm)病毒是人群中的主要流感病毒株。在一些国家,它还越过了物种壁垒,感染了火鸡和猪。因此,迫切需要开发对多种动物有效的疫苗。先前我们已经证明,将温度敏感突变引入禽类H9N2病毒的PB2和PB1基因,并在PB1中插入血凝素(HA)标签,导致两只鸡的减毒(att)疫苗骨架和老鼠。由于新的大流行毒株是三重重组(TR)病毒,因此我们选择将双重减毒修饰引入猪样TR病毒分离株A / turkey / OH / 313053/04(H3N2)(ty / 04),目的是生产减毒活疫苗(LAIV)。这种基因修饰的骨架在高温下损害了聚合酶的活性并限制了病毒的生长。使用ty / 04 att骨架生成的两种H1N1候选疫苗的体内特征表明,该疫苗在小鼠中高度减毒,如无疾病迹象,复制受限以及呼吸道组织病理学改变最小。使用基于ty / 04 att的疫苗进行的单次免疫可以完全保护小鼠免受致命的H1N1pdm病毒感染。更重要的是,使用ty / 04 att-H1N1候选疫苗对猪进行疫苗接种后,对2009 H1N1大流行性病毒进行了气管内积极攻击后,可产生杀菌免疫力。我们的研究突出了ty / 04 att疫苗平台的安全性及其作为生产人类和家畜减毒活疫苗的主要供体菌株的潜力。

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