Targeting Antigens for Universal Influenza Vaccine Development

被引:20
|
作者
Nguyen, Quyen-Thi [1 ,2 ]
Choi, Young-Ki [1 ,2 ,3 ]
机构
[1] Chungbuk Natl Univ, Coll Med, Cheongju 28644, South Korea
[2] Chungbuk Natl Univ, Med Res Inst, Cheongju 28644, South Korea
[3] Chungbuk Natl Univ, Zoonot Infect Dis Res Ctr, Cheongju 28644, South Korea
来源
VIRUSES-BASEL | 2021年 / 13卷 / 06期
基金
新加坡国家研究基金会;
关键词
influenza; universal vaccine; antigen; immune response; VIRUS-LIKE PARTICLES; IMMUNE-RESPONSE; GLOBULAR HEAD; NEURAMINIDASE ANTIBODY; A(H3N2) VIRUSES; B VIRUS; MONOCLONAL-ANTIBODY; HEMAGGLUTININ STALK; BROAD PROTECTION; CROSS-PROTECTION;
D O I
10.3390/v13060973
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Traditional influenza vaccines generate strain-specific antibodies which cannot provide protection against divergent influenza virus strains. Further, due to frequent antigenic shifts and drift of influenza viruses, annual reformulation and revaccination are required in order to match circulating strains. Thus, the development of a universal influenza vaccine (UIV) is critical for long-term protection against all seasonal influenza virus strains, as well as to provide protection against a potential pandemic virus. One of the most important strategies in the development of UIVs is the selection of optimal targeting antigens to generate broadly cross-reactive neutralizing antibodies or cross-reactive T cell responses against divergent influenza virus strains. However, each type of target antigen for UIVs has advantages and limitations for the generation of sufficient immune responses against divergent influenza viruses. Herein, we review current strategies and perspectives regarding the use of antigens, including hemagglutinin, neuraminidase, matrix proteins, and internal proteins, for universal influenza vaccine development.
引用
收藏
页数:21
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