Szécsi Judit, Boson Bertrand, Johnsson Per, Dupeyrot-Lacas Pia, Matrosovich Mikhail, Klenk Hans-Dieter, Klatzmann David, Volchkov Viktor, Cosset François-Loïc
INSERM, U758, F-69007 Lyon, France.
Virol J. 2006 Sep 3;3:70. doi: 10.1186/1743-422X-3-70.
There is an urgent need to develop novel approaches to vaccination against the emerging, highly pathogenic avian influenza viruses. Here, we engineered influenza viral-like particles (Flu-VLPs) derived from retroviral core particles that mimic the properties of the viral surface of two highly pathogenic influenza viruses of either H7N1 or H5N1 antigenic subtype. We demonstrate that, upon recovery of viral RNAs from a field strain, one can easily generate expression vectors that encode the HA, NA and M2 surface proteins of either virus and prepare high-titre Flu-VLPs. We characterise these Flu-VLPs incorporating the HA, NA and M2 proteins and we show that they induce high-titre neutralising antibodies in mice.
迫切需要开发针对新出现的高致病性禽流感病毒的新型疫苗接种方法。在此,我们构建了源自逆转录病毒核心颗粒的流感病毒样颗粒(Flu-VLPs),其模拟了两种H7N1或H5N1抗原亚型的高致病性流感病毒的病毒表面特性。我们证明,从田间毒株中回收病毒RNA后,可以轻松生成编码这两种病毒的血凝素(HA)、神经氨酸酶(NA)和M2表面蛋白的表达载体,并制备高滴度的Flu-VLPs。我们对包含HA、NA和M2蛋白的这些Flu-VLPs进行了表征,并表明它们能在小鼠体内诱导产生高滴度的中和抗体。