Broadly neutralizing antibodies against influenza viruses

被引:119
作者
Laursen, Nick S. [1 ]
Wilson, Ian A. [1 ,2 ]
机构
[1] Scripps Res Inst, Dept Integrat Struct & Computat Biol, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
基金
美国国家卫生研究院;
关键词
Influenza; Broadly neutralizing antibodies; Hemagglutinin; RECEPTOR-BINDING SITE; A VIRUSES; B VIRUS; NEURAMINIDASE INHIBITORS; MONOCLONAL-ANTIBODIES; HEMAGGLUTININ; VACCINES; RECOGNITION; EPITOPE; H5N1;
D O I
10.1016/j.antiviral.2013.03.021
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Despite available antivirals and vaccines, influenza continues to be a major cause of mortality worldwide. Vaccination generally induces an effective, but strain-specific antibody response. As the virus continually evolves, new vaccines have to be administered almost annually when a novel strain becomes dominant. Furthermore, the sporadic emerging resistance to neuraminidase inhibitors among circulating strains suggests an urgent need for new therapeutic agents. Recently, several cross-reactive antibodies have been described, which neutralize an unprecedented spectrum of influenza viruses. These broadly neutralizing antibodies generally target conserved functional regions on the major influenza surface glycoprotein hemagglutinin (HA). The characterization of their neutralization breadth and epitopes on HA could stimulate the development of new antibody-based antivirals and broader influenza vaccines. This article forms part of a symposium in Antiviral Research on "Treatment of influenza: targeting the virus or the host." (C) 2013 Published by Elsevier B.V.
引用
收藏
页码:476 / 483
页数:8
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