Heads, stalks and everything else: how can antibodies eradicate influenza as a human disease?

被引:74
作者
Neu, Karlynn E. [1 ]
Dunand, Carole J. Henry [2 ]
Wilson, Patrick C. [1 ,2 ]
机构
[1] Univ Chicago, Comm Immunol, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Med, Rheumatol Sect, Knapp Ctr Lupus & Immunol Res, 5841 S Maryland Ave, Chicago, IL 60637 USA
基金
美国国家卫生研究院;
关键词
RECEPTOR-BINDING SITE; CONSERVED NEUTRALIZING EPITOPE; VIRUS HEMAGGLUTININ; A VIRUSES; MONOCLONAL-ANTIBODIES; H5N1; VACCINATION; GLOBULAR HEAD; NEURAMINIDASE; RECOGNITION; RESPONSES;
D O I
10.1016/j.coi.2016.05.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Current seasonal influenza virus vaccines are effective against infection but they have to be reformulated on a regular basis to counter antigenic variations. The majority of the antibodies induced in response to seasonal vaccination are strain specific. However, antibodies targeting conserved epitopes on the hemagglutinin protein have been identified and they offer broad protection. Most of these antibodies bind the hemagglutinin stalk domain and are generated from preexisting memory B cells. Broadly protective stalk-biased responses induced by antigenically divergent influenza strains, in concert with prior immunity, are sufficient to eradicate seasonally circulating strains. Future vaccine trials should aim to harness and maintain such a response with the realistic goal of developing a universal influenza vaccine.
引用
收藏
页码:48 / 55
页数:8
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