Virus-like particles as universal influenza vaccines

被引:69
作者
Kang, Sang-Moo [1 ,2 ]
Kim, Min-Chul [3 ,4 ]
Compans, Richard W. [3 ,4 ]
机构
[1] Georgia State Univ, Ctr Inflammat Immun & Infect, Atlanta, GA 30303 USA
[2] Georgia State Univ, Dept Biol, Atlanta, GA 30303 USA
[3] Emory Univ, Sch Med, Dept Microbiol & Immunol, Atlanta, GA 30322 USA
[4] Emory Univ, Sch Med, Emory Vaccine Ctr, Atlanta, GA 30322 USA
关键词
adjuvant; HA stalk domain; influenza; M2; NA; universal vaccine; VLPs; HEMAGGLUTININ MEMBRANE GLYCOPROTEIN; ADJUVANT CELLULAR MECHANISMS; EXPRESSING H5 HEMAGGLUTININ; PROTECTIVE IMMUNE-RESPONSES; M2 PROTON CHANNEL; CD8(+) T-CELLS; A-VIRUS; DENDRITIC CELLS; LETHAL INFLUENZA; EXTRACELLULAR DOMAIN;
D O I
10.1586/ERV.12.70
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Expert Rev. Vaccines 11(8), 995-1007 (2012) Current influenza vaccines are primarily targeted to induce immunity to the influenza virus strain-specific hemagglutinin antigen and are not effective in controlling outbreaks of new pandemic viruses. An approach for developing universal vaccines is to present highly conserved antigenic epitopes in an immunogenic conformation such as virus-like particles (VLPs) together with an adjuvant to enhance the vaccine immunogenicity. In this review, the authors focus on conserved antigenic targets and molecular adjuvants that were presented in VLPs. Conserved antigenic targets that include the hemagglutinin stalk domain, the external domain of influenza M2 and neuraminidase are discussed in addition to molecular adjuvants that are engineered to be incorporated into VLPs in a membrane-anchored form.
引用
收藏
页码:995 / 1007
页数:13
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