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Healthy human subjects have CD4+ T cells directed against H5N1 influenza virus.健康人体受试者拥有针对H5N1流感病毒的CD4 + T细胞。
J Immunol. 2008 Feb 1;180(3):1758-68. doi: 10.4049/jimmunol.180.3.1758.
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A combination in-ovo vaccine for avian influenza virus and Newcastle disease virus.一种用于禽流感病毒和新城疫病毒的鸡胚内联合疫苗。
Vaccine. 2008 Jan 24;26(4):522-31. doi: 10.1016/j.vaccine.2007.11.032. Epub 2007 Dec 3.
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Potent immunogenicity and efficacy of a universal influenza vaccine candidate comprising a recombinant fusion protein linking influenza M2e to the TLR5 ligand flagellin.一种包含将流感病毒M2e与Toll样受体5(TLR5)配体鞭毛蛋白连接起来的重组融合蛋白的通用流感疫苗候选物具有强大的免疫原性和效力。
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Physical interventions to interrupt or reduce the spread of respiratory viruses: systematic review.中断或减少呼吸道病毒传播的物理干预措施:系统评价
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A case-control study of elderly patients with acute respiratory illness: effect of influenza vaccination on admission to hospital in winter 2003-2004.
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Effectiveness of influenza vaccine in the community-dwelling elderly.流感疫苗对社区老年人的有效性。
N Engl J Med. 2007 Oct 4;357(14):1373-81. doi: 10.1056/NEJMoa070844.
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Development and evaluation of an Influenza virus subtype H7N2 vaccine candidate for pandemic preparedness.用于大流行防范的H7N2流感病毒候选疫苗的研发与评估。
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Generation of an attenuated H5N1 avian influenza virus vaccine with all eight genes from avian viruses.利用来自禽流感病毒的全部八个基因生成减毒H5N1禽流感病毒疫苗。
Vaccine. 2007 Oct 16;25(42):7379-84. doi: 10.1016/j.vaccine.2007.08.011. Epub 2007 Aug 24.
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Partial protection against H5N1 influenza in mice with a single dose of a chimpanzee adenovirus vector expressing nucleoprotein.用单剂量表达核蛋白的黑猩猩腺病毒载体对小鼠提供针对H5N1流感的部分保护。
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10
Antigen sparing and cross-reactive immunity with an adjuvanted rH5N1 prototype pandemic influenza vaccine: a randomised controlled trial.一种佐剂化重组H5N1大流行性流感原型疫苗的抗原节省和交叉反应性免疫:一项随机对照试验。
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大流行性流感疫苗

Pandemic influenza vaccines.

作者信息

DiMenna Lauren J, Ertl Hildegund C J

机构信息

The Wistar Institute, 3601 Spruce St, Philadelphia, PA 19104, USA.

出版信息

Curr Top Microbiol Immunol. 2009;333:291-321. doi: 10.1007/978-3-540-92165-3_15.

DOI:10.1007/978-3-540-92165-3_15
PMID:19768412
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7121491/
Abstract

Since their compositions remain uncertain, universal pandemic vaccines are yet to be created. They would aim to protect globally against pandemic influenza viruses that have not yet evolved. Thus they differ from seasonal vaccines to influenza virus, which are updated annually in spring to incorporate the latest circulating viruses, and are then produced and delivered before the peak influenza season starts in late fall and winter. The efficacy of seasonal vaccines is linked to their ability to induce virus-neutralizing antibodies, which provide subtype-specific protection against influenza A viruses. If pandemic vaccines were designed to resemble current vaccines in terms of composition and mode of action, they would have to be developed, tested, and mass-produced after the onset of a pandemic, once the causative virus had been identified. The logistic problems of generating a pandemic vaccine from scratch, conducting preclinical testing, and producing billions of doses within a few months for global distribution are enormous and may well be insurmountable. Alternatively, the scientific community could step up efforts to generate a universal vaccine against influenza A viruses that provides broadly cross-reactive protection through the induction of antibodies or T cells to conserved regions of the virus.

摘要

由于其成分仍不确定,通用大流行疫苗尚未研制出来。它们旨在为全球提供针对尚未演变的大流行性流感病毒的保护。因此,它们不同于流感病毒季节性疫苗,后者在春季每年更新以纳入最新流行的病毒,然后在秋季末和冬季流感季节高峰开始之前生产和交付。季节性疫苗的效力与其诱导病毒中和抗体的能力有关,这些抗体可提供针对甲型流感病毒的亚型特异性保护。如果大流行疫苗在成分和作用方式上设计得与当前疫苗相似,那么一旦确定致病病毒,就必须在大流行开始后进行研发、测试和大规模生产。从零开始生产大流行疫苗、进行临床前测试并在几个月内生产数十亿剂用于全球分发的后勤问题巨大,很可能无法克服。或者,科学界可以加大力度研发一种针对甲型流感病毒的通用疫苗,通过诱导针对病毒保守区域的抗体或T细胞来提供广泛的交叉反应保护。