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Vaccination with Vesicular Stomatitis Virus-Vectored Chimeric Hemagglutinins Protects Mice against Divergent Influenza Virus Challenge Strains.用水泡性口炎病毒载体嵌合血凝素疫苗接种可保护小鼠免受不同流感病毒攻击毒株的侵害。
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本文引用的文献

1
Intramuscular immunization with a vesicular stomatitis virus recombinant expressing the influenza hemagglutinin provides post-exposure protection against lethal influenza challenge.肌肉内接种表达流感血凝素的水疱性口炎病毒重组疫苗可提供针对致死性流感攻击的暴露后保护。
Vaccine. 2009 Dec 10;28(1):79-89. doi: 10.1016/j.vaccine.2009.09.112. Epub 2009 Oct 9.
2
Humoral and cellular immune responses to split-virion H5N1 influenza vaccine in young and elderly adults.年轻人和老年人对裂解病毒H5N1流感疫苗的体液免疫和细胞免疫反应。
Vaccine. 2009 Nov 16;27(49):6918-25. doi: 10.1016/j.vaccine.2009.08.110. Epub 2009 Sep 15.
3
Influenza vaccine strain selection and recent studies on the global migration of seasonal influenza viruses.流感疫苗株的选择及近期关于季节性流感病毒全球传播的研究。
Vaccine. 2008 Sep 12;26 Suppl 4:D31-4. doi: 10.1016/j.vaccine.2008.07.078.
4
MF59-adjuvanted H5N1 vaccine induces immunologic memory and heterotypic antibody responses in non-elderly and elderly adults.MF59佐剂H5N1疫苗在非老年人和老年人中诱导免疫记忆和异型抗体反应。
PLoS One. 2009;4(2):e4384. doi: 10.1371/journal.pone.0004384. Epub 2009 Feb 6.
5
Vesicular stomatitis virus-based ebola vaccine is well-tolerated and protects immunocompromised nonhuman primates.基于水疱性口炎病毒的埃博拉疫苗耐受性良好,可保护免疫功能低下的非人灵长类动物。
PLoS Pathog. 2008 Nov;4(11):e1000225. doi: 10.1371/journal.ppat.1000225. Epub 2008 Nov 28.
6
An avian live attenuated master backbone for potential use in epidemic and pandemic influenza vaccines.一种可用于流行性和大流行性流感疫苗的禽源减毒主骨架。
J Gen Virol. 2008 Nov;89(Pt 11):2682-2690. doi: 10.1099/vir.0.2008/004143-0.
7
Vesicular stomatitis virus-based vaccines protect nonhuman primates against aerosol challenge with Ebola and Marburg viruses.基于水泡性口炎病毒的疫苗可保护非人灵长类动物免受埃博拉病毒和马尔堡病毒的气溶胶攻击。
Vaccine. 2008 Dec 9;26(52):6894-900. doi: 10.1016/j.vaccine.2008.09.082. Epub 2008 Oct 18.
8
Prepandemic influenza vaccine H5N1 (split virion, inactivated, adjuvanted) [Prepandrix]: a review of its use as an active immunization against influenza A subtype H5N1 virus.大流行前甲型H5N1流感疫苗(裂解病毒、灭活、佐剂)[Prepandrix]:作为预防甲型H5N1流感病毒主动免疫制剂的应用综述
BioDrugs. 2008;22(5):279-92. doi: 10.2165/00063030-200822050-00001.
9
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.
10
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。
J Infect Dis. 2008 Apr 15;197(8):1185-8. doi: 10.1086/529522.

基于强感染力水泡性口炎病毒的禽流感疫苗可提供针对异源挑战的长期有效免疫性。

Potent vesicular stomatitis virus-based avian influenza vaccines provide long-term sterilizing immunity against heterologous challenge.

机构信息

Department of Pathology, Yale University School of Medicine, 310 Cedar St., LH 315, New Haven, CT 06520, USA.

出版信息

J Virol. 2010 May;84(9):4611-8. doi: 10.1128/JVI.02637-09. Epub 2010 Feb 24.

DOI:10.1128/JVI.02637-09
PMID:20181720
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2863739/
Abstract

The emergence in 1997 and continuance today of a highly lethal H5N1 avian influenza virus (AIV) causing human disease has raised concern about an impending pandemic and the need for a vaccine to prepare for such an occurrence. We previously generated an efficacious vesicular stomatitis virus (VSV)-based AIV vaccine expressing H5 hemagglutinin (HA) from the fifth genomic position of VSV (J. A. Schwartz et al., Virology 366:166-173, 2007). Here we have generated and characterized VSV-based vaccines that express the A/Hong Kong/156/1997 (clade 0) H5 HA from the first position of the VSV genome. These vectors induce broadly cross-neutralizing antibodies against homologous and heterologous H5N1 viruses of different clades in mice. The vaccines provide complete protection against morbidity and mortality after heterologous challenge with clade 0 and clade 1 strains in animals even 1 year after vaccination. Postchallenge pulmonary virus loads show that these vectors provide sterilizing immunity. Therefore, VSV-based AIV vaccines are potent, broadly cross-protective pandemic vaccine candidates.

摘要

1997 年出现并持续至今的高致死性 H5N1 禽流感病毒(AIV)导致人类患病,这引发了人们对即将到来的大流行的担忧,也需要一种疫苗来为此类情况做好准备。我们之前生成了一种有效的基于水疱性口炎病毒(VSV)的 AIV 疫苗,该疫苗在 VSV 的第五个基因组位置表达 H5 血凝素(HA)(J. A. Schwartz 等人,《病毒学》366:166-173, 2007)。在这里,我们生成并表征了基于 VSV 的疫苗,这些疫苗在 VSV 基因组的第一个位置表达 A/Hong Kong/156/1997(0 谱系)H5 HA。这些载体在小鼠中诱导针对同源和异源 H5N1 病毒的广泛交叉中和抗体,不同谱系。疫苗在接种后 1 年,即使在接种后 1 年,也能为动物提供针对 0 谱系和 1 谱系菌株的异源挑战的发病率和死亡率的完全保护。接种后肺部病毒载量表明,这些载体提供了杀菌免疫。因此,基于 VSV 的 AIV 疫苗是有效的、广泛交叉保护的大流行疫苗候选物。