Starch-based NP act as antigen delivery systems without immunomodulating effect

被引:6
作者
Fasquelle, Francois [1 ]
Dubuquoy, Laurent [2 ]
Betbeder, Didier [1 ]
机构
[1] Vaxinano, Loos, France
[2] Univ Lille, U1286 INFINITE Inst Translat Res Inflammat, CHU Lille, Inserm, Lille, France
关键词
VACCINE ADJUVANTS; IMMUNE-RESPONSES; EPITHELIAL-CELLS; MUCOSAL; NANOPARTICLES; INNATE; ENDOCYTOSIS; MECHANISMS; EXPRESSION; INFECTION;
D O I
10.1371/journal.pone.0272234
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
The nasal route of immunization has become a real alternative to injections. It is indeed described as more efficient at inducing immune protection, since it initiates both mucosal and systemic immunity, thus protecting against both the infection itself and the transmission of pathogens by the host. However, the use of immunomodulators should be limited since they induce inflammation. Here we investigated in vitro the mechanisms underlying the enhancement of antigen immunogenicity by starch nanoparticles (NPL) delivery systems in H292 epithelial cells, as well as the NPL's immunomodulatory effect. We observed that NPL had no intrinsic immunomodulatory effect but enhanced the immunogenicity of an E. coli lysate (Ag) merely by increasing its intracellular delivery. Moreover, we demonstrated the importance of the NPL density on their efficiency by comparing reticulated (NPL) and non-reticulated particles (NPLAR). These results show that an efficient delivery system is sufficient to induce a mucosal immune response without the use of immunomodulators.
引用
收藏
页数:17
相关论文
共 55 条
[51]   Pulmonary delivery of ISCOMATRIX influenza vaccine induces both systemic and mucosal immunity with antigen dose sparing [J].
Wee, J. L. K. ;
Scheerlinck, J-P Y. ;
Snibson, K. J. ;
Edwards, S. ;
Pearse, M. ;
Quinn, C. ;
Sutton, P. .
MUCOSAL IMMUNOLOGY, 2008, 1 (06) :489-496
[52]   Immunogenicity of the RTS,S/AS01 malaria vaccine and implications for duration of vaccine efficacy: secondary analysis of data from a phase 3 randomised controlled trial [J].
White, Michael T. ;
Verity, Robert ;
Griffin, Jamie T. ;
Asante, Kwaku Poku ;
Owusu-Agyei, Seth ;
Greenwood, Brian ;
Drakeley, Chris ;
Gesase, Samwel ;
Lusingu, John ;
Ansong, Daniel ;
Adjei, Samuel ;
Agbenyega, Tsiri ;
Ogutu, Bernhards ;
Otieno, Lucas ;
Otieno, Walter ;
Agnandji, Selidji T. ;
Lell, Bertrand ;
Kremsner, Peter ;
Hoffman, Irving ;
Martinson, Francis ;
Kamthunzu, Portia ;
Tinto, Halidou ;
Valea, Innocent ;
Sorgho, Hermann ;
Oneko, Martina ;
Otieno, Kephas ;
Hamel, Mary J. ;
Salim, Nahya ;
Mtoro, Ali ;
Abdulla, Salim ;
Aide, Pedro ;
Sacarlal, Jahit ;
Aponte, John J. ;
Njuguna, Patricia ;
Marsh, Kevin ;
Bejon, Philip ;
Riley, Eleanor M. ;
Ghani, Azra C. .
LANCET INFECTIOUS DISEASES, 2015, 15 (12) :1450-1458
[53]   Inducible Bronchus-Associated Lymphoid Tissue Elicited by a Protein Cage Nanoparticle Enhances Protection in Mice against Diverse Respiratory Viruses [J].
Wiley, James A. ;
Richert, Laura E. ;
Swain, Steve D. ;
Harmsen, Ann ;
Barnard, Dale L. ;
Randall, Troy D. ;
Jutila, Mark ;
Douglas, Trevor ;
Broomell, Chris ;
Young, Mark ;
Harmsen, Allen .
PLOS ONE, 2009, 4 (09)
[54]   A single dose of an adenovirus-vectored vaccine provides protection against SARS-CoV-2 challenge [J].
Wu, Shipo ;
Zhong, Gongxun ;
Zhang, Jun ;
Shuai, Lei ;
Zhang, Zhe ;
Wen, Zhiyuan ;
Wang, Busen ;
Zhao, Zhenghao ;
Song, Xiaohong ;
Chen, Yi ;
Liu, Renqiang ;
Fu, Ling ;
Zhang, Jinlong ;
Guo, Qiang ;
Wang, Chong ;
Yang, Yilong ;
Fang, Ting ;
Lv, Peng ;
Wang, Jinliang ;
Xu, Junjie ;
Li, Jianmin ;
Yu, Changming ;
Hou, Lihua ;
Bu, Zhigao ;
Chen, Wei .
NATURE COMMUNICATIONS, 2020, 11 (01)
[55]   Cellular Uptake of Elastic Nanoparticles [J].
Yi, Xin ;
Shi, Xinghua ;
Gao, Huajian .
PHYSICAL REVIEW LETTERS, 2011, 107 (09)