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Protection against mouse and avian influenza A strains via vaccination with a combination of conserved proteins NP, M1 and NS1

机译:通过结合保守蛋白NP,M1和NS1的疫苗接种预防小鼠和禽流感A株

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Background Experimental data accumulated over more than a decade indicate that cross-strain protection against influenza may be achieved by immunization with conserved influenza proteins. At the same time, the efficacy of immunization schemes designed along these lines and involving internal influenza proteins, mostly NP and M1, has not been sufficient. Objective To test the immunogenicity and protective efficacy of DNA vaccination with a combination of NP, M1 and NS1 genes of influenza virus. Methods The immunogenicity and protective efficacy of DNA vaccination with NP, M1 and NS1 was tested in mice and chickens. Mice were challenged with mouse-adapted viral strains H3N2 and H5N2 and chicken challenged with avian H5N3 virus. Results In these settings, wild-type NS1 did not impede the cellular and humoral response to NP/M1 immunization in vivo . Moreover, addition of NS1-encoding plasmid to the NP/M1 immunization protocol resulted in a significantly increased protective efficacy in vivo . Conclusions The addition of NS1 to an influenza immunization regimen based on conserved proteins bears promise. It is feasible that upon further genetic modification of these and additional conserved influenza proteins, providing for their higher safety, expression and immunogenicity, a recombinant vaccine based on several structural and non-structural proteins or their epitopes will offer broad anti-influenza protection in a wide range of species.
机译:背景技术十多年来积累的实验数据表明,可以通过使用保守的流感蛋白进行免疫来实现针对流感的跨株保护。同时,按照这些思路设计并涉及内部流感蛋白(主要是NP和M1)的免疫方案的功效还不够。目的检测流感病毒NP,M1和NS1基因组合的DNA疫苗的免疫原性和防护效果。方法检测NP,M1和NS1基因DNA疫苗在小鼠和鸡体内的免疫原性和保护作用。用小鼠适应病毒株H3N2和H5N2攻击小鼠,并用禽H5N3病毒攻击鸡。结果在这些情况下,野生型NS1不会阻碍体内对NP / M1免疫的细胞和体液反应。而且,将编码NS1的质粒添加到NP / M1免疫方案中导致体内保护作用的显着提高。结论在基于保守蛋白的流感免疫方案中添加NS1具有希望。可行的是,对这些和其他保守的流感蛋白进行进一步的基因修饰,以提供更高的安全性,表达和免疫原性,基于几种结构和非结构蛋白或其表位的重组疫苗将在流感病毒中提供广泛的抗流感保护。种类繁多。

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