CAS OpenIR  > 生化工程国家重点实验室
Exploration of Antigen Induced CaCO3 Nanoparticles for Therapeutic Vaccine
Wang, Shuang1,2; Ni, Dezhi1; Yue, Hua1; Luo, Nana1; Xi, Xiaobo1,2; Wang, Yugang3; Shi, Min3; Wei, Wei1; Ma, Guanghui1,2,4
2018-04-05
Source PublicationSMALL
ISSN1613-6810
Volume14Issue:14
Abstract

Therapeutic vaccines possess particular advantages and show promising potential to combat burdening diseases, such as acquired immunodeficiency syndrome, hepatitis, and even cancers. An efficient therapeutic vaccine would strengthen the immune system and eventually eliminate target cells through cytotoxic T lymphocytes (CTLs). Unfortunately, insufficient efficacy in triggering such an adaptive immune response is a problem that remains unsolved. To achieve efficient cellular immunity, antigen-presenting cells must capture and further cross-present disease-associated antigens to CD8 T cells via major histocompatibility complex I molecules. Here, a biomimetic strategy is developed to fabricate hierarchical ovalbumin@CaCO3 nanoparticles (OVA@NP, approximate to 500 nm) under the templating effect of antigen OVA. Taking advantage of the unique physicochemical properties of crystalline vaterite, cluster structure, and high loading, OVA@NP can efficiently ferry cargo antigen to dendritic cells and blast lysosomes for antigen escape to the cytoplasm. In addition, the first evidence that the physical stress from generated CO2 induces autophagy through the LC3/Beclin 1 pathways is presented. These outcomes cooperatively promote antigen cross-presentation, elicit CD8 T cell proliferation, ignite a potent and specific CTL response, and finally achieve prominent tumor therapy effects.

KeywordAutophagy Calcium Carbonate Cross-presentation Lysosome Escape Nanoparticles
SubtypeArticle
WOS HeadingsScience & Technology ; Physical Sciences ; Technology
DOI10.1002/smll.201704272
Indexed BySCI
Language英语
WOS KeywordCross-presentation ; Dendritic Cells ; Cancer-immunotherapy ; Liposomal System ; Delivery ; Responses ; Immunity ; Peptide ; Biomineralization ; Ovalbumin
WOS Research AreaChemistry ; Science & Technology - Other Topics ; Materials Science ; Physics
WOS SubjectChemistry, Multidisciplinary ; Chemistry, Physical ; Nanoscience & Nanotechnology ; Materials Science, Multidisciplinary ; Physics, Applied ; Physics, Condensed Matter
Funding OrganizationNational Key R&D Program of China(2017YFA0207900) ; National Science and Technology Major Projects for
WOS IDWOS:000429579100024
Citation statistics
Cited Times:3[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.ipe.ac.cn/handle/122111/24180
Collection生化工程国家重点实验室
Affiliation1.Chinese Acad Sci, Inst Proc Engn, State Key Lab Biochem Engn, Beijing 100190, Peoples R China
2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
3.Shanghai Jiao Tong Univ, Sch Med, Shanghai Tongren Hosp, Dept Gastroenterol, Shanghai 200336, Peoples R China
4.Jiangsu Natl Synerget Innovat Ctr Adv Mat, Nanjing 211816, Jiangsu, Peoples R China
Recommended Citation
GB/T 7714
Wang, Shuang,Ni, Dezhi,Yue, Hua,et al. Exploration of Antigen Induced CaCO3 Nanoparticles for Therapeutic Vaccine[J]. SMALL,2018,14(14).
APA Wang, Shuang.,Ni, Dezhi.,Yue, Hua.,Luo, Nana.,Xi, Xiaobo.,...&Ma, Guanghui.(2018).Exploration of Antigen Induced CaCO3 Nanoparticles for Therapeutic Vaccine.SMALL,14(14).
MLA Wang, Shuang,et al."Exploration of Antigen Induced CaCO3 Nanoparticles for Therapeutic Vaccine".SMALL 14.14(2018).
Files in This Item:
File Name/Size DocType Version Access License
Exploration of Antig(10937KB)期刊论文出版稿限制开放CC BY-NC-SAApplication Full Text
Related Services
Recommend this item
Bookmark
Usage statistics
Export to Endnote
Google Scholar
Similar articles in Google Scholar
[Wang, Shuang]'s Articles
[Ni, Dezhi]'s Articles
[Yue, Hua]'s Articles
Baidu academic
Similar articles in Baidu academic
[Wang, Shuang]'s Articles
[Ni, Dezhi]'s Articles
[Yue, Hua]'s Articles
Bing Scholar
Similar articles in Bing Scholar
[Wang, Shuang]'s Articles
[Ni, Dezhi]'s Articles
[Yue, Hua]'s Articles
Terms of Use
No data!
Social Bookmark/Share
All comments (0)
No comment.
 

Items in the repository are protected by copyright, with all rights reserved, unless otherwise indicated.