Breadth of Antibody Responses during Influenza Virus Infection and Vaccination

被引:14
|
作者
Kubo, Masato [1 ,2 ]
Miyauchi, Kosuke [1 ]
机构
[1] RIKEN Yokohama Inst, Ctr Integrat Med Sci IMS, Lab Cytokine Regulat, Tsurumi Ku, 1-7-22 Suehiro Cho, Yokohama, Kanagawa 2300045, Japan
[2] Tokyo Univ Sci, Div Mol Pathol, Res Inst Biomed Sci, 2669 Yamazaki, Noda, Chiba 2780022, Japan
基金
日本学术振兴会;
关键词
HEMAGGLUTININ STALK ANTIBODIES; GERMINAL CENTER SELECTION; B-CELL RESPONSES; CD4; T-CELLS; FOLLICULAR-HELPER; NEUTRALIZING ANTIBODIES; SECRETORY COMPONENT; PROTECTIVE IMMUNITY; AFFINITY MATURATION; ANTIGENIC STRUCTURE;
D O I
10.1016/j.it.2020.03.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Influenza viruses are a major public health problem, causing severe respiratory diseases. Vaccines offer the effective protective strategy against influenza virus infection. However, the systemic and adaptive immune responses to infection and vaccination are quite different. Inactivated vaccines are the best available countermeasure to induce effective antibodies against the emerged virus, but the response is narrow compared with potential breadth of virus infection. There is solid evidence to indicate that antibody responses to natural infection are relatively broad and exhibit quite different immunodominance patterns. Furthermore, T follicular helper cells (T-FH) and germinal center (GC) responses play a central role in generating broad protective antibodies. In this review, we discuss recent advances on the contribution of T-FH and GC responses to the breadth of antibody responses.
引用
收藏
页码:394 / 405
页数:12
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