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基于普马拉病毒合成M基因的DNA疫苗的构建及非临床测试。

Construction and nonclinical testing of a Puumala virus synthetic M gene-based DNA vaccine.

作者信息

Brocato R L, Josleyn M J, Wahl-Jensen V, Schmaljohn C S, Hooper J W

机构信息

Virology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA.

出版信息

Clin Vaccine Immunol. 2013 Feb;20(2):218-26. doi: 10.1128/CVI.00546-12. Epub 2012 Dec 12.

Abstract

Puumala virus (PUUV) is a causative agent of hemorrhagic fever with renal syndrome (HFRS). Although PUUV-associated HFRS does not result in high case-fatality rates, the social and economic impact is considerable. There is no licensed vaccine or specific therapeutic to prevent or treat HFRS. Here we report the synthesis of a codon-optimized, full-length M segment open reading frame and its cloning into a DNA vaccine vector to produce the plasmid pWRG/PUU-M(s2). pWRG/PUU-M(s2) delivered by gene gun produced high-titer neutralizing antibodies in hamsters and nonhuman primates. Vaccination with pWRG/PUU-M(s2) protected hamsters against infection with PUUV but not against infection by related HFRS-associated hantaviruses. Unexpectedly, vaccination protected hamsters in a lethal disease model of Andes virus (ANDV) in the absence of ANDV cross-neutralizing antibodies. This is the first evidence that an experimental DNA vaccine for HFRS can provide protection in a hantavirus lethal disease model.

摘要

普马拉病毒(PUUV)是肾综合征出血热(HFRS)的病原体。虽然与PUUV相关的HFRS不会导致高病死率,但社会和经济影响相当大。目前尚无预防或治疗HFRS的许可疫苗或特异性疗法。在此,我们报告了密码子优化的全长M段开放阅读框的合成及其克隆到DNA疫苗载体中,以产生质粒pWRG/PUU-M(s2)。通过基因枪递送的pWRG/PUU-M(s2)在仓鼠和非人灵长类动物中产生了高滴度的中和抗体。用pWRG/PUU-M(s2)进行疫苗接种可保护仓鼠免受PUUV感染,但不能预防相关的与HFRS相关的汉坦病毒感染。出乎意料的是,在没有安第斯病毒(ANDV)交叉中和抗体的情况下,疫苗接种在ANDV致死疾病模型中保护了仓鼠。这是首个证据表明,一种用于HFRS的实验性DNA疫苗可在汉坦病毒致死疾病模型中提供保护。

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