A Perspective on Nanoparticle Universal Influenza Vaccines

被引:35
|
作者
Deng, Lei [1 ]
Wang, Bao-Zhong [1 ]
机构
[1] Georgia State Univ, Ctr Inflammat Immun & Infect, 145 Piedmont Ave SE, Atlanta, GA 30302 USA
来源
ACS INFECTIOUS DISEASES | 2018年 / 4卷 / 12期
基金
美国国家卫生研究院;
关键词
prophylaxis; virus-like particle; self-assembling; long-lasting; headless hemagglutinin; matrix protein 2; VIRUS-LIKE PARTICLES; IMPROVED CROSS-PROTECTION; GOLD NANOPARTICLES; IMMUNE-RESPONSES; HEMAGGLUTININ TRIMERS; EXTRACELLULAR DOMAIN; ALVEOLAR MACROPHAGES; MONOCLONAL-ANTIBODY; PANDEMIC INFLUENZA; MATRIX PROTEIN-2;
D O I
10.1021/acsinfecdis.8b00206
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Annually recurring seasonal influenza causes massive economic loss and poses severe threats to public health worldwide. The current seasonal influenza vaccines are the most effective means of preventing influenza infections but possess major weaknesses. Seasonal influenza vaccines require annual updating of the vaccine strains. However, it is an unreachable task to accurately predict the future circulating strains. Vaccines with mismatched strains dramatically compromise the vaccine efficacy. In addition, the seasonal influenza vaccines are ineffective against an unpredictable pandemic. A universal influenza vaccine would overcome these weaknesses of the seasonal vaccines and abolish the threat of influenza pandemics. One approach under investigation is to design influenza vaccine immunogens based on conserved, type-specific amino acid sequences and conformational epitopes, rather than strain-specific. Such vaccines can elicit broadly reactive humoral and cellular immunity. Universal influenza vaccine development has intensively employed nanotechnology because the structural and morphological properties of nanoparticles dramatically improve vaccine immunogenicity and the induced immunity duration. Layered protein nanoparticles can decrease off-target immune responses, fine-tune antigen recognition and processing, and facilitate comprehensive immune response induction. Herein, we review the designs of effective nanoparticle universal influenza vaccines, the recent discoveries of specific nanoparticle features that contribute to immunogenicity enhancement, and recent progress in clinical trials.
引用
收藏
页码:1656 / 1665
页数:19
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