Cationic micelle based vaccine induced potent humoral immune response through enhancing antigen uptake and formation of germinal center
Cationic micelle based vaccine induced potent humoral immune response through enhancing antigen uptake and formation of germinal center
复制标题
基于阳离子胶束的疫苗通过增强抗原摄取和生发中心的形成诱导有效的体液免疫反应
DOI:
10.1016/j.colsurfb.2015.07.079
复制
发表时间:
2015-11-01
影响因子:
5.8
通讯作者:
Li, Xingyi
中科院分区:
文献类型:
--
作者:
Luo, Zichao;Shi, Shuai;Li, Xingyi
Nanoparticles have been proven to be an effective vaccine delivery system that can boost immune responses to subunit vaccines. Herein, we developed and characterized a cationic polymeric polyethylene glycol(2000)-poly epsilon-caprolactone(2000)-polyethylenimine(2000) (mPEG(2000)-PCL2000-g-PEI2000) micelle as a potent vaccine delivery system to boost the immune response in vivo. The micelles that we developed exhibited great antigen-loading capability and minimal cytotoxicity in vitro. Meanwhile, micelles facilitated OVA antigen uptake by dendritic cells both in vitro and in vivo. More importantly, a micelle-formulated OVA vaccine could significantly promote anti-OVA antibody production by 190-fold and potently enhance T cell proliferation and the secretion of IL-5 and IFN-gamma. We attributed these effects to its ability to promote antigen uptake, antigen deposition, and germinal center formation. In conclusion, the mPEG(2000)-PCL2000-PEI2000 micelle that we developed has potential as potent vaccine delivery system to induce Th2 immune response. (C) 2015 Elsevier B.V. All rights reserved.