Clinical vaccine development for H5N1 influenza

被引:22
|
作者
Clegg, Christopher H. [1 ]
Rininger, Joseph A. [2 ]
Baldwin, Susan L. [3 ]
机构
[1] TRIA Biosci Corp, Seattle, WA 98102 USA
[2] CaroGen Corp, Hamden, CT 06518 USA
[3] Infect Dis Res Inst, Seattle, WA 98102 USA
基金
美国国家卫生研究院;
关键词
adjuvant; dose sparing; emulsion; H5N1; pandemic influenza; recombinant protein; Toll-like receptor 4; vaccine; CROSS-REACTIVE IMMUNITY; VIRUS-LIKE PARTICLE; PANDEMIC INFLUENZA; HEALTHY-ADULTS; PHASE-I; IMMUNOGENICITY; SAFETY; HEMAGGLUTININ; ADJUVANT; FERRETS;
D O I
10.1586/14760584.2013.811178
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
H5N1 is a highly pathogenic avian influenza virus that can cause severe disease and death in humans. H5N1 is spreading rapidly in bird populations and there is great concern that this virus will begin to transmit between people and cause a global crisis. Vaccines are the cornerstone strategy for combating avian influenza but there are complex challenges for pandemic preparedness including the unpredictability of the vaccine target and the manufacturing requirement for rapid deployment. The less-than-optimal response against the 2009 H1N1 pandemic unmasked the limitations associated with influenza vaccine production and in 2010, the President's Council of Advisors on Science and Technology re-emphasized the need for new recombinant-based vaccines and adjuvants that can shorten production cycles, maximize immunogenicity and satisfy global demand. In this article, the authors review the efforts spent in developing an effective vaccine for H5N1 influenza and summarize clinical studies that highlight the progress made to date.
引用
收藏
页码:767 / 777
页数:11
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