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Influenza Other Respir Viruses. 2007 May;1(3):105-12. doi: 10.1111/j.1750-2659.2007.00016.x.
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Heterosubtypic protection against pathogenic human and avian influenza viruses via in vivo electroporation of synthetic consensus DNA antigens.通过体内电穿孔导入合成共有DNA抗原实现对致病性人类和禽流感病毒的异源亚型保护。
PLoS One. 2008 Jun 25;3(6):e2517. doi: 10.1371/journal.pone.0002517.
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A clinical trial of a whole-virus H5N1 vaccine derived from cell culture.一项源自细胞培养的全病毒H5N1疫苗的临床试验。
N Engl J Med. 2008 Jun 12;358(24):2573-84. doi: 10.1056/NEJMoa073121.
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Plasmid DNA-based vaccines protect mice and ferrets against lethal challenge with A/Vietnam/1203/04 (H5N1) influenza virus.基于质粒DNA的疫苗可保护小鼠和雪貂免受A/越南/1203/04(H5N1)流感病毒的致死性攻击。
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Potentiation of an anthrax DNA vaccine with electroporation.通过电穿孔增强炭疽DNA疫苗效果
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A broadly protective vaccine against globally dispersed clade 1 and clade 2 H5N1 influenza viruses.一种针对全球广泛传播的1类和2类H5N1流感病毒的广谱保护性疫苗。
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The relative immunogenicity of DNA vaccines delivered by the intramuscular needle injection, electroporation and gene gun methods.通过肌肉注射、电穿孔和基因枪方法递送的DNA疫苗的相对免疫原性。
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Recruitment of antigen-presenting cells to the site of inoculation and augmentation of human immunodeficiency virus type 1 DNA vaccine immunogenicity by in vivo electroporation.通过体内电穿孔将抗原呈递细胞募集至接种部位并增强1型人类免疫缺陷病毒DNA疫苗的免疫原性。
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Cell culture (Vero) derived whole virus (H5N1) vaccine based on wild-type virus strain induces cross-protective immune responses.基于野生型病毒株的细胞培养(Vero)衍生全病毒(H5N1)疫苗可诱导交叉保护性免疫反应。
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一种基于血凝素的DNA疫苗,可保护小鼠免受不同H5N1流感病毒的侵害。

A consensus-hemagglutinin-based DNA vaccine that protects mice against divergent H5N1 influenza viruses.

作者信息

Chen Ming-Wei, Cheng Ting-Jen Rachel, Huang Yaoxing, Jan Jia-Tsrong, Ma Shiou-Hwa, Yu Alice L, Wong Chi-Huey, Ho David D

机构信息

Genomics Research Center, Academia Sinica, Taipei 115, Taiwan.

出版信息

Proc Natl Acad Sci U S A. 2008 Sep 9;105(36):13538-43. doi: 10.1073/pnas.0806901105. Epub 2008 Sep 2.

DOI:10.1073/pnas.0806901105
PMID:18765801
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2533225/
Abstract

H5N1 influenza viruses have spread extensively among wild birds and domestic poultry. Cross-species transmission of these viruses to humans has been documented in over 380 cases, with a mortality rate of approximately 60%. There is great concern that a H5N1 virus would acquire the ability to spread efficiently between humans, thereby becoming a pandemic threat. An H5N1 influenza vaccine must, therefore, be an integral part of any pandemic preparedness plan. However, traditional methods of making influenza vaccines have yet to produce a candidate that could induce potently neutralizing antibodies against divergent strains of H5N1 influenza viruses. To address this need, we generated a consensus H5N1 hemagglutinin (HA) sequence based on data available in early 2006. This sequence was then optimized for protein expression before being inserted into a DNA plasmid (pCHA5). Immunizing mice with pCHA5, delivered intramuscularly via electroporation, elicited antibodies that neutralized a panel of virions that have been pseudotyped with the HA from various H5N1 viruses (clades 1, 2.1, 2.2, 2.3.2, and 2.3.4). Moreover, immunization with pCHA5 in mice conferred complete (clades 1 and 2.2) or significant (clade 2.1) protection from H5N1 virus challenges. We conclude that this vaccine, based on a consensus HA, could induce broad protection against divergent H5N1 influenza viruses and thus warrants further study.

摘要

H5N1流感病毒已在野生鸟类和家禽中广泛传播。这些病毒跨物种传播给人类的情况已有超过380例记录,死亡率约为60%。人们极为担心H5N1病毒会获得在人类之间有效传播的能力,从而成为一种大流行威胁。因此,H5N1流感疫苗必须成为任何大流行防范计划的一个组成部分。然而,传统的流感疫苗制备方法尚未产生一种能够诱导针对不同株H5N1流感病毒产生强效中和抗体的候选疫苗。为满足这一需求,我们根据2006年初可得的数据生成了一个H5N1血凝素(HA)共有序列。然后对该序列进行蛋白质表达优化,再将其插入DNA质粒(pCHA5)中。通过电穿孔经肌肉注射用pCHA5免疫小鼠,可引发抗体,这些抗体能中和一组用来自各种H5N1病毒(1、2.1、2.2、2.3.2和2.3.4分支)的HA进行假型化的病毒粒子。此外,用pCHA5免疫小鼠可使其对H5N1病毒攻击获得完全(1和2.2分支)或显著(2.1分支)的保护。我们得出结论,这种基于共有HA的疫苗能够诱导针对不同H5N1流感病毒的广泛保护,因此值得进一步研究。