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首页> 外文期刊>Vaccine >A novel Sin Nombre virus DNA vaccine and its inclusion in a candidate pan-hantavirus vaccine against hantavirus pulmonary syndrome (HPS) and hemorrhagic fever with renal syndrome (HFRS)
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A novel Sin Nombre virus DNA vaccine and its inclusion in a candidate pan-hantavirus vaccine against hantavirus pulmonary syndrome (HPS) and hemorrhagic fever with renal syndrome (HFRS)

机译:一种新型的辛诺布尔病毒DNA疫苗,并将其包含在针对汉坦病毒性肺综合征(HPS)和肾综合征出血热(HFRS)的全汉坦病毒候选疫苗中

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摘要

Sin Nombre virus (SNV; family Bunyaviridae, genus Hantavirus) causes a hemorrhagic fever known as hantavirus pulmonary syndrome (HPS) in North America. There have been approximately 200 fatal cases of HPS in the United States since 1993, predominantly in healthy working-age males (case fatality rate 35%). There are no FDA-approved vaccines or drugs to prevent or treat HPS. Previously, we reported that hantavirus vaccines based on the full-length M gene segment of Andes virus (ANDV) for HPS in South America, and Hantaan virus (HTNV) and Puumala virus (PUUV) for hemorrhagic fever with renal syndrome (HFRS) in Eurasia, all elicited high-titer neutralizing antibodies in animal models. HFRS is more prevalent than HPS (>20,000 cases per year) but less pathogenic (case fatality rate 1-15%). Here, we report the construction and testing of a SNV full-length M gene-based DNA vaccine to prevent HPS. Rabbits vaccinated with the SNV DNA vaccine by muscle electroporation (mEP) developed high titers of neutralizing antibodies. Furthermore, hamsters vaccinated three times with the SNV DNA vaccine using a gene gun were completely protected against SNV infection. This is the first vaccine of any kind that specifically elicits high-titer neutralizing antibodies against SNV. To test the possibility of producing a pan-hantavirus vaccine, rabbits were vaccinated by mEP with an HPS mix (ANDV and SNV plasmids), or HFRS mix (HTNV and PUUV plasmids), or HPS/HFRS mix (all four plasmids). The HPS mix and HFRS mix elicited neutralizing antibodies predominantly against ANDV/SNV and HTNV/PUUV, respectively. Furthermore, the HPS/HFRS mix elicited neutralizing antibodies against all four viruses. These findings demonstrate a pan-hantavirus vaccine using a mixed-plasmid DNA vaccine approach is feasible and warrants further development. (C) 2013 The Authors. Published by Elsevier Ltd. All rights reserved.
机译:罪孽病毒(SNV;布尼亚病毒科家族,汉塔病毒属)在北美引起出血热,称为汉塔病毒肺综合征(HPS)。自1993年以来,美国大约有200例HPS致命病例,主要发生在健康的工作年龄男性中(病死率35%)。没有FDA批准的预防或治疗HPS的疫苗或药物。以前,我们报道过汉坦病毒疫苗基于南美地区HPS的安第斯病毒(ANDV)的全长M基因片段,而汉坦病毒(HTNV)和Puumala病毒(PUUV)则用于治疗肾综合征出血热(HFRS)。欧亚大陆都在动物模型中引发了高滴度中和抗体。 HFRS比HPS流行(每年> 20,000例),但致病性较小(病死率1-15%)。在这里,我们报告了基于SNV全长M基因的DNA疫苗的构建和测试,以预防HPS。通过肌肉电穿孔(mEP)接种SNV DNA疫苗的兔子产生了高滴度的中和抗体。此外,使用基因枪用SNV DNA疫苗接种过3次的仓鼠可以完全预防SNV感染。这是第一种特异性引发针对SNV的高滴度中和抗体的疫苗。为了测试生产全汉坦病毒疫苗的可能性,将mHP与HPS混合物(ANDV和SNV质粒)或HFRS混合物(HTNV和PUUV质粒)或HPS / HFRS混合物(所有四个质粒)一起接种兔。 HPS混合物和HFRS混合物分别引发主要针对ANDV / SNV和HTNV / PUUV的中和抗体。此外,HPS / HFRS混合物引发了针对所有四种病毒的中和抗体。这些发现表明,使用混合质粒DNA疫苗方法的全汉坦病毒疫苗是可行的,有待进一步开发。 (C)2013作者。由Elsevier Ltd.出版。保留所有权利。

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