Improving pandemic H5N1 influenza vaccines by combining different vaccine platforms

被引:26
|
作者
Luke, Catherine J. [1 ]
Subbarao, Kanta [1 ]
机构
[1] NIAID, Emerging Resp Viruses Sect, Infect Dis Lab, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
influenza vaccine; pandemic influenza vaccine; prime boost; T-CELL RESPONSES; A VIRUS; IMMUNE-RESPONSES; MF59-ADJUVANTED INFLUENZA; ANTIBODY-RESPONSES; GLOBAL MORTALITY; BOOSTER RESPONSE; CLINICAL-TRIAL; IMMUNOGENICITY; SAFETY;
D O I
10.1586/14760584.2014.922416
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A variety of platforms are being explored for the development of vaccines for pandemic influenza. Observations that traditional inactivated subvirion vaccines and live-attenuated vaccines against H5 and some H7 influenza viruses were poorly immunogenic spurred efforts to evaluate new approaches, including whole virus vaccines, higher doses of antigen, addition of adjuvants and combinations of different vaccine modalities in heterologous prime-boost regimens to potentiate immune responses. Results from clinical trials of prime-boost regimens have been very promising. Further studies are needed to determine optimal combinations of platforms, intervals between doses of vaccines and the logistics of deployment in pre-pandemic and early pandemic settings.
引用
收藏
页码:873 / 883
页数:11
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