Targeting B cell responses in universal influenza vaccine design

被引:46
作者
Kaur, Kaval [1 ,3 ]
Sullivan, Meghan [2 ,3 ]
Wilson, Patrick C. [1 ,3 ]
机构
[1] Univ Chicago, Comm Immunol, Chicago, IL 60637 USA
[2] Univ Chicago, Comm Mol Pathol & Mol Med, Chicago, IL 60637 USA
[3] Univ Chicago, Dept Med, Rheumatol Sect, Knapp Ctr Lupus & Immunol Res, Chicago, IL 60637 USA
基金
美国国家卫生研究院;
关键词
HUMAN MONOCLONAL-ANTIBODIES; VIRUS HEMAGGLUTININ; A VIRUS; RECEPTOR-BINDING; STRUCTURAL BASIS; MEMBRANE-FUSION; PROTECTS MICE; SIALIC-ACID; NEURAMINIDASE; PEPTIDE;
D O I
10.1016/j.it.2011.08.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Since its first administration in the 1940s, the influenza vaccine has provided tremendous relief against influenza infections. However, time has revealed the ultimate limit of the vaccine and the call for its reinvention has now come, just as we are beginning to appreciate the antibody immune responses vital in preventing infections. New strategies to design the influenza vaccine rely on selectively inducing broadly neutralizing antibodies that are specific for highly conserved viral epitopes. Such approaches take us away from the limited range of protection provided by current seasonal influenza vaccines and towards a future with a pan-influenza vaccine capable of providing universal strain coverage.
引用
收藏
页码:524 / 531
页数:8
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