Application of built-in adjuvants for epitope-based vaccines

被引:70
|
作者
Lei, Yao [1 ,2 ]
Zhao, Furong [1 ,2 ]
Shao, Junjun [1 ,2 ]
Li, Yangfan [1 ,2 ]
Li, Shifang [1 ,2 ]
Chang, Huiyun [1 ,2 ]
Zhang, Yongguang [1 ,2 ]
机构
[1] Chinese Acad Agr Sci, Lanzhou Vet Res Inst, State Key Lab Vet Etiol Biol, OIE Natl Foot & Mouth Dis Reference Lab, Lanzhou, Gansu, Peoples R China
[2] Jiangsu Coinnovat Ctr Prevent & Control Importan, Yangzhou, Jiangsu, Peoples R China
来源
PEERJ | 2019年 / 6卷
关键词
Built-in adjuvants; Epitope-based vaccines; Biological carriers; Nanoparticles; VIRUS-LIKE PARTICLES; HEAT-SHOCK-PROTEIN; OUTER-MEMBRANE VESICLES; TOBACCO-MOSAIC-VIRUS; T-CELL RESPONSES; MAJOR IMMUNODOMINANT REGION; NEXT-GENERATION VACCINES; FLAGELLIN FUSION VACCINE; A STREPTOCOCCAL VACCINE; B CORE ANTIGEN;
D O I
10.7717/peerj.6185
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Several studies have shown that epitope vaccines exhibit substantial advantages over conventional vaccines. However, epitope vaccines are associated with limited immunity, which can be overcome by conjugating antigenic epitopes with built-in adjuvants (e.g., some carrier proteins or new biomaterials) with special properties, including immunologic specificity, good biosecurity and biocompatibility, and the ability to vastly improve the immune response of epitope vaccines. When designing epitope vaccines, the following types of built-in adjuvants are typically considered: (1) pattern recognition receptor ligands (i.e., toll-like receptors); (2) virus-like particle carrier platforms; (3) bacterial toxin proteins; and (4) novel potential delivery systems (e.g., self-assembled peptide nanoparticles, lipid core peptides, and polymeric or inorganic nanoparticles). This review primarily discusses the current and prospective applications of these built-in adjuvants (i.e., biological carriers) to provide some references for the future design of epitope-based vaccines.
引用
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页数:48
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