表位
免疫系统
计算生物学
抗原
线性表位
病毒学
生物
免疫学
作者
Yao Lei,Furong Zhao,Jing Shao,Yangfan Li,Shifang Li,Huiyun Chang,Yongguang Zhang
出处
期刊:PeerJ
[PeerJ]
日期:2019-01-14
卷期号:6: e6185-e6185
被引量:85
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.
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