Novel Vaccine Delivery System Induces Robust Humoral and Cellular Immune Responses Based on Multiple Mechanisms
Wang, Yue-Qi1,2; Wu, Jie1; Fan, Qing-Ze1,2; Zhou, Meng1; Yue, Zhan-Guo1,2; Ma, Guang-Hui1; Su, Zhi-Guo1
刊名ADVANCED HEALTHCARE MATERIALS
2014-05-01
卷号3期号:5页码:670-681
关键词hydrogels particulate delivery system adjuvants quaternized chitosan H5N1 split vaccines
ISSN号2192-2640
其他题名Adv. Healthc. Mater.
中文摘要Aiming to enhance the immunogenicity of H5N1 split vaccine, the development of a novel antigen delivery system based on quaternized chitosan hydrogel microparticles (Gel MPs) with multiple mechanisms of immunity enhancement is attempted. Gel MPs based on ionic cross-linking are prepared in a simple and mild way. Gel MPs are superior as a vaccine delivery system due to their ability to: 1) enhance cellular uptake and endosomal escape of antigens in dendritic cells (DCs); 2) significantly activate DCs; 3) form an antigen depot and recruit immunity cells to improve antigen capture. Further in vivo investigation shows that Gel MPs, in comparison to aluminum salts (Alum), LPS, and covalent cross-linking quaternized chitosan MPs (GC MPs), induce higher humoral and cellular immune responses with a mixed Th1/Th2 immunity. In conclusion, these results demonstrate that Gel MPs are efficient antigen delivery vehicles based on multiple mechanisms to enhance both humoral and cellular immune responses against H5N1 split antigen.
英文摘要Aiming to enhance the immunogenicity of H5N1 split vaccine, the development of a novel antigen delivery system based on quaternized chitosan hydrogel microparticles (Gel MPs) with multiple mechanisms of immunity enhancement is attempted. Gel MPs based on ionic cross-linking are prepared in a simple and mild way. Gel MPs are superior as a vaccine delivery system due to their ability to: 1) enhance cellular uptake and endosomal escape of antigens in dendritic cells (DCs); 2) significantly activate DCs; 3) form an antigen depot and recruit immunity cells to improve antigen capture. Further in vivo investigation shows that Gel MPs, in comparison to aluminum salts (Alum), LPS, and covalent cross-linking quaternized chitosan MPs (GC MPs), induce higher humoral and cellular immune responses with a mixed Th1/Th2 immunity. In conclusion, these results demonstrate that Gel MPs are efficient antigen delivery vehicles based on multiple mechanisms to enhance both humoral and cellular immune responses against H5N1 split antigen.
WOS标题词Science & Technology ; Technology
类目[WOS]Materials Science, Biomaterials
研究领域[WOS]Materials Science
关键词[WOS]DENDRITIC CELLS ; INFLUENZA VACCINES ; VIRAL-INFECTION ; DRUG-DELIVERY ; H5N1 VIRUS ; IN-VITRO ; T-CELLS ; CHITOSAN ; ADJUVANT ; ACTIVATION
收录类别SCI
原文出处://WOS:000335730200005
语种英语
WOS记录号WOS:000335730200005
公开日期2014-08-28
内容类型期刊论文
版本出版稿
源URL[http://ir.ipe.ac.cn/handle/122111/10986]  
专题过程工程研究所_研究所(批量导入)
作者单位1.Chinese Acad Sci, Natl Key Lab Biochem Engn, Key Lab Biopharmaceut Prod & Formulat Engn, Inst Proc Engn, Beijing 100190, Peoples R China
2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
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GB/T 7714
Wang, Yue-Qi,Wu, Jie,Fan, Qing-Ze,et al. Novel Vaccine Delivery System Induces Robust Humoral and Cellular Immune Responses Based on Multiple Mechanisms[J]. ADVANCED HEALTHCARE MATERIALS,2014,3(5):670-681.
APA Wang, Yue-Qi.,Wu, Jie.,Fan, Qing-Ze.,Zhou, Meng.,Yue, Zhan-Guo.,...&Su, Zhi-Guo.(2014).Novel Vaccine Delivery System Induces Robust Humoral and Cellular Immune Responses Based on Multiple Mechanisms.ADVANCED HEALTHCARE MATERIALS,3(5),670-681.
MLA Wang, Yue-Qi,et al."Novel Vaccine Delivery System Induces Robust Humoral and Cellular Immune Responses Based on Multiple Mechanisms".ADVANCED HEALTHCARE MATERIALS 3.5(2014):670-681.
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