Cross-protective immunity to influenza A viruses

被引:87
作者
Epstein, Suzanne L. [1 ]
Price, Graeme E. [1 ]
机构
[1] US FDA, Div Cellular & Gene Therapies, Ctr Biol Evaluat & Res, Rockville, MD 20852 USA
关键词
animal models; conserved antigens; cross-protection; heterosubtypic immunity; human; influenza; pandemic; subtypes; universal vaccine; vaccine; CYTOTOXIC T-LYMPHOCYTES; HETEROSUBTYPIC IMMUNITY; M2; PROTEIN; LETHAL INFLUENZA; CELL RESPONSES; HETEROTYPIC IMMUNITY; H5N1; INFLUENZA; EXTRACELLULAR DOMAIN; MATRIX PROTEIN-2; BROAD-SPECTRUM;
D O I
10.1586/ERV.10.123
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Antigenic changes in influenza virus occur gradually, owing to mutations (antigenic drift), and abruptly, owing to reassortment among subtypes (antigenic shift). Availability of strain-matched vaccines often lags behind these changes, resulting in a shortfall in public health. In animal models, cross-protection by vaccines based on conserved antigens does not completely prevent infection, but greatly reduces morbidity, mortality, virus replication and, thus, viral shedding and spread. Such immunity is especially effective and long-lasting with mucosal administration. Cross-protective immunity in humans is controversial, but is suggested by some epidemiological findings. 'Universal' vaccines protective against all influenza A viruses might substantially reduce severity of infection and limit spread of disease during outbreaks. These vaccines could be used 'off the shelf' early in an outbreak or pandemic, before strain-matched vaccines are available.
引用
收藏
页码:1325 / 1341
页数:17
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