Application of built-in adjuvants for epitope-based vaccines

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...

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Main Authors: Yao Lei, Furong Zhao, Junjun Shao, Yangfan Li, Shifang Li, Huiyun Chang, Yongguang Zhang
Format: Article
Language:English
Published: PeerJ Inc. 2019-01-01
Series:PeerJ
Subjects:
Online Access:https://peerj.com/articles/6185.pdf
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author Yao Lei
Furong Zhao
Junjun Shao
Yangfan Li
Shifang Li
Huiyun Chang
Yongguang Zhang
author_facet Yao Lei
Furong Zhao
Junjun Shao
Yangfan Li
Shifang Li
Huiyun Chang
Yongguang Zhang
author_sort Yao Lei
collection DOAJ
description 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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spelling doaj.art-a131755f778c4256a954898f1264f8302023-12-03T10:43:17ZengPeerJ Inc.PeerJ2167-83592019-01-016e618510.7717/peerj.6185Application of built-in adjuvants for epitope-based vaccinesYao Lei0Furong Zhao1Junjun Shao2Yangfan Li3Shifang Li4Huiyun Chang5Yongguang Zhang6State Key Laboratory of Veterinary Etiological Biology, OIE/National Foot-and-Mouth Disease Reference Laboratory, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, ChinaState Key Laboratory of Veterinary Etiological Biology, OIE/National Foot-and-Mouth Disease Reference Laboratory, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, ChinaState Key Laboratory of Veterinary Etiological Biology, OIE/National Foot-and-Mouth Disease Reference Laboratory, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, ChinaState Key Laboratory of Veterinary Etiological Biology, OIE/National Foot-and-Mouth Disease Reference Laboratory, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, ChinaState Key Laboratory of Veterinary Etiological Biology, OIE/National Foot-and-Mouth Disease Reference Laboratory, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, ChinaState Key Laboratory of Veterinary Etiological Biology, OIE/National Foot-and-Mouth Disease Reference Laboratory, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, ChinaState Key Laboratory of Veterinary Etiological Biology, OIE/National Foot-and-Mouth Disease Reference Laboratory, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, ChinaSeveral 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.https://peerj.com/articles/6185.pdfBuilt-in adjuvantsEpitope-based vaccinesBiological carriersNanoparticles
spellingShingle Yao Lei
Furong Zhao
Junjun Shao
Yangfan Li
Shifang Li
Huiyun Chang
Yongguang Zhang
Application of built-in adjuvants for epitope-based vaccines
PeerJ
Built-in adjuvants
Epitope-based vaccines
Biological carriers
Nanoparticles
title Application of built-in adjuvants for epitope-based vaccines
title_full Application of built-in adjuvants for epitope-based vaccines
title_fullStr Application of built-in adjuvants for epitope-based vaccines
title_full_unstemmed Application of built-in adjuvants for epitope-based vaccines
title_short Application of built-in adjuvants for epitope-based vaccines
title_sort application of built in adjuvants for epitope based vaccines
topic Built-in adjuvants
Epitope-based vaccines
Biological carriers
Nanoparticles
url https://peerj.com/articles/6185.pdf
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