Respiratory Viruses and Virus-like Particle Vaccine Development: How Far Have We Advanced?

被引:11
作者
Chu, Ki-Back [1 ,2 ]
Quan, Fu-Shi [1 ,2 ,3 ]
机构
[1] Kyung Hee Univ, Core Res Inst CRI, Med Res Ctr Bioreact React Oxygen Species, Seoul 02447, South Korea
[2] Kyung Hee Univ, Biomed Sci Inst, Core Res Inst CRI, Seoul 02447, South Korea
[3] Kyung Hee Univ, Sch Med, Dept Med Zool, Seoul 02447, South Korea
来源
VIRUSES-BASEL | 2023年 / 15卷 / 02期
基金
新加坡国家研究基金会;
关键词
virus-like particle; influenza virus; respiratory syncytial virus; SARS-CoV-2; vaccine; H1N1; 2009; VACCINE; SYNCYTIAL VIRUS; INFLUENZA VACCINE; NEUTRALIZING ANTIBODIES; EXTRACELLULAR DOMAIN; PROTECTIVE IMMUNITY; LONG-TERM; IMMUNOGENICITY; DISEASE; HEMAGGLUTININ;
D O I
10.3390/v15020392
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
With technological advancements enabling globalization, the intercontinental transmission of pathogens has become much easier. Respiratory viruses are one such group of pathogens that require constant monitoring since their outbreak leads to massive public health crises, as exemplified by the influenza virus, respiratory syncytial virus (RSV), and the recent coronavirus disease 2019 (COVID-19) outbreak caused by the SARS-CoV-2. To prevent the transmission of these highly contagious viruses, developing prophylactic tools, such as vaccines, is of considerable interest to the scientific community. Virus-like particles (VLPs) are highly sought after as vaccine platforms for their safety and immunogenicity profiles. Although several VLP-based vaccines against hepatitis B and human papillomavirus have been approved for clinical use by the United States Food and Drug Administration, VLP vaccines against the three aforementioned respiratory viruses are lacking. Here, we summarize the most recent progress in pre-clinical and clinical VLP vaccine development. We also outline various strategies that contributed to improving the efficacy of vaccines against each virus and briefly discuss the stability aspect of VLPs that makes it a highly desired vaccine platform.
引用
收藏
页数:25
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