Virus-like particles as a highly efficient vaccine platform: Diversity of targets and production systems and advances in clinical development

被引:450
作者
Kushnir, Natasha [1 ]
Streatfield, Stephen J. [1 ]
Yusibov, Vidadi [1 ]
机构
[1] Fraunhofer USA Ctr Mol Biotechnol, Newark, DE 19711 USA
关键词
Virus-like particle; Subunit vaccine; Clinical development; Heterologous expression system; Virosome; HEPATITIS-B SURFACE; HUMAN-PAPILLOMAVIRUS TYPE-16; MAJOR CAPSID PROTEIN; HUMAN-IMMUNODEFICIENCY-VIRUS; PROTECTIVE IMMUNE-RESPONSES; ROTAVIRUS-LIKE PARTICLES; HIGH-LEVEL EXPRESSION; BURSAL DISEASE VIRUS; CYTOTOXIC T-CELLS; HEAT-LABILE TOXIN;
D O I
10.1016/j.vaccine.2012.10.083
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Virus-like particles (VLPs) are a class of subunit vaccines that differentiate themselves from soluble recombinant antigens by stronger protective immunogenicity associated with the VLP structure. Like parental viruses, VLPs can be either non-enveloped or enveloped, and they can form following expression of one or several viral structural proteins in a recombinant heterologous system. Depending on the complexity of the VLP, it can be produced in either a prokaryotic or eukaryotic expression system using target-encoding recombinant vectors, or in some cases can be assembled in cell-free conditions. To date, a wide variety of VLP-based candidate vaccines targeting various viral, bacterial, parasitic and fungal pathogens, as well as non-infectious diseases, have been produced in different expression systems. Some VLPs have entered clinical development and a few have been licensed and commercialized. This article reviews VLP-based vaccines produced in different systems, their immunogenicity in animal models and their status in clinical development. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:58 / 83
页数:26
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