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本文引用的文献

1
Universal influenza virus vaccines: need for clinical trials.通用流感病毒疫苗:临床试验的必要性。
Nat Immunol. 2014 Jan;15(1):3-5. doi: 10.1038/ni.2761.
2
Expression of functional recombinant hemagglutinin and neuraminidase proteins from the novel H7N9 influenza virus using the baculovirus expression system.利用杆状病毒表达系统表达新型H7N9流感病毒的功能性重组血凝素和神经氨酸酶蛋白。
J Vis Exp. 2013 Nov 6(81):e51112. doi: 10.3791/51112.
3
Adjuvants and immunization strategies to induce influenza virus hemagglutinin stalk antibodies.诱导流感病毒血凝素茎部抗体的佐剂和免疫策略。
PLoS One. 2013 Nov 6;8(11):e79194. doi: 10.1371/journal.pone.0079194. eCollection 2013.
4
Influenza virus hemagglutinin stalk-based antibodies and vaccines.基于流感病毒血凝素茎部的抗体和疫苗。
Curr Opin Virol. 2013 Oct;3(5):521-30. doi: 10.1016/j.coviro.2013.07.007. Epub 2013 Aug 24.
5
Neutralizing antibodies against previously encountered influenza virus strains increase over time: a longitudinal analysis.针对先前遇到的流感病毒株的中和抗体随时间推移而增加:一项纵向分析。
Sci Transl Med. 2013 Aug 14;5(198):198ra107. doi: 10.1126/scitranslmed.3006637.
6
Hemagglutinin stalk-based universal vaccine constructs protect against group 2 influenza A viruses.基于血凝素茎部的通用疫苗构建体可预防 2 类流感 A 病毒。
J Virol. 2013 Oct;87(19):10435-46. doi: 10.1128/JVI.01715-13. Epub 2013 Jul 31.
7
Origin and molecular characteristics of a novel 2013 avian influenza A(H6N1) virus causing human infection in Taiwan.2013年台湾地区一株致人感染的新型甲型禽流感病毒(H6N1)的起源及分子特征
Clin Infect Dis. 2013 Nov;57(9):1367-8. doi: 10.1093/cid/cit479. Epub 2013 Jul 23.
8
Association between adverse clinical outcome in human disease caused by novel influenza A H7N9 virus and sustained viral shedding and emergence of antiviral resistance.新型甲型 H7N9 流感病毒导致的人类疾病不良临床结局与病毒持续排出和抗病毒耐药性的出现之间的关联。
Lancet. 2013 Jun 29;381(9885):2273-9. doi: 10.1016/S0140-6736(13)61125-3. Epub 2013 May 29.
9
Protection against lethal influenza with a viral mimic.用病毒模拟物预防致命性流感。
J Virol. 2013 Aug;87(15):8591-605. doi: 10.1128/JVI.01081-13. Epub 2013 May 29.
10
Prolonged influenza virus shedding and emergence of antiviral resistance in immunocompromised patients and ferrets.免疫功能低下患者和雪貂中流感病毒持续排出和出现抗病毒耐药性。
PLoS Pathog. 2013;9(5):e1003343. doi: 10.1371/journal.ppat.1003343. Epub 2013 May 23.

评估雪貂基于流感病毒血凝素茎的免疫原性。

Assessment of influenza virus hemagglutinin stalk-based immunity in ferrets.

机构信息

Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.

出版信息

J Virol. 2014 Mar;88(6):3432-42. doi: 10.1128/JVI.03004-13. Epub 2014 Jan 8.

DOI:10.1128/JVI.03004-13
PMID:24403585
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3957929/
Abstract

UNLABELLED

Therapeutic monoclonal antibodies that target the conserved stalk domain of the influenza virus hemagglutinin and stalk-based universal influenza virus vaccine strategies are being developed as promising countermeasures for influenza virus infections. The pan-H1-reactive monoclonal antibody 6F12 has been extensively characterized and shows broad efficacy against divergent H1N1 strains in the mouse model. Here we demonstrate its efficacy against a pandemic H1N1 challenge virus in the ferret model of influenza disease. Furthermore, we recently developed a universal influenza virus vaccine strategy based on chimeric hemagglutinin constructs that focuses the immune response on the conserved stalk domain of the hemagglutinin. Here we set out to test this vaccination strategy in the ferret model. Both strategies, pretreatment of animals with a stalk-reactive monoclonal antibody and vaccination with chimeric hemagglutinin-based constructs, were able to significantly reduce viral titers in nasal turbinates, lungs, and olfactory bulbs. In addition, vaccinated animals also showed reduced nasal wash viral titers. In summary, both strategies showed efficacy in reducing viral loads after an influenza virus challenge in the ferret model.

IMPORTANCE

Influenza virus hemagglutinin stalk-reactive antibodies tend to be less potent yet are more broadly reactive and can neutralize seasonal and pandemic influenza virus strains. The ferret model was used to assess the potential of hemagglutinin stalk-based immunity to provide protection against influenza virus infection. The novelty and significance of the findings described in this report support the development of vaccines stimulating stalk-specific antibody responses.

摘要

未加标签

正在开发针对流感病毒血凝素保守茎部的治疗性单克隆抗体和基于茎部的通用流感病毒疫苗策略,作为流感病毒感染的有希望的对策。广泛针对 H1 反应的单克隆抗体 6F12 已得到广泛表征,在小鼠模型中显示出对不同 H1N1 株的广泛疗效。在这里,我们证明了它在流感疾病的雪貂模型中对大流行性 H1N1 挑战病毒的疗效。此外,我们最近开发了一种基于嵌合血凝素构建体的通用流感病毒疫苗策略,该策略将免疫反应集中在血凝素的保守茎部上。在这里,我们着手在雪貂模型中测试这种疫苗接种策略。用针对茎部的单克隆抗体预处理动物和用嵌合血凝素为基础的构建体进行疫苗接种,都能显著降低鼻鼻甲、肺和嗅球中的病毒滴度。此外,接种疫苗的动物的鼻洗液病毒滴度也降低了。总之,这两种策略在雪貂模型中流感病毒挑战后均能有效降低病毒载量。

重要性

流感病毒血凝素茎部反应性抗体往往效力较低,但更广泛地具有反应性,并且可以中和季节性和大流行性流感病毒株。雪貂模型被用于评估血凝素茎部免疫提供针对流感病毒感染的保护的潜力。本报告中描述的发现的新颖性和重要性支持了刺激茎部特异性抗体反应的疫苗的开发。