Nanoporous polyelectrolyte vaccine microcarriers. A formulation platform for enhancing humoral and cellular immune responses

被引:17
作者
De Koker, Stefaan [1 ,2 ]
Fierens, Kaat [3 ,4 ]
Dierendonck, Marijke [1 ]
De Rycke, Riet [3 ,5 ,6 ]
Lambrecht, Bart N. [3 ,4 ]
Grooten, Johan [2 ]
Remon, Jean Paul [1 ]
De Geest, Bruno G. [1 ]
机构
[1] Univ Ghent, Dept Pharmaceut, B-9000 Ghent, Belgium
[2] Univ Ghent, Dept Biomed Mol Biol, B-9000 Ghent, Belgium
[3] Univ Ghent, VIB Inflammat Res Ctr, B-9000 Ghent, Belgium
[4] Univ Hosp Ghent, Dept Resp Med, Ghent, Belgium
[5] Univ Ghent VIB, Dept Plant Syst Biol, B-9052 Ghent, Belgium
[6] Univ Ghent, Dept Plant Biotechnol & Bioinformat, B-9000 Ghent, Belgium
关键词
Microparticles; Vaccines; Antigens; Polyelectrolytes; Spray drying; ANTIGEN CROSS-PRESENTATION; DENDRITIC CELLS; MULTILAYER CAPSULES; DELIVERY; MICROPARTICLES; MICROCAPSULES; BIOCOMPATIBILITY; MICROSPHERES; CANCER;
D O I
10.1016/j.jconrel.2014.07.043
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this paper we report on the design, characterization and immuno-biological evaluation of nanoporous polyelectrolyte microparticles as vaccine carrier. Relative to soluble antigen, formulation of antigen as a sub-10 mu m particle can strongly enhance antigen-specific cellular immune responses. The latter is crucial to confer protective immunity against intracellular pathogens and for anti-cancer vaccines. However, a major bottleneck in microparticulate vaccine formulation is the development of generic strategies that afford antigen encapsulation under benign and scalable conditions. Our strategy is based on spray drying of a dilute aqueous solution of antigen, oppositely charged polyelectrolytes and mannitol as a pore-forming component. The obtained solid microparticles can be redispersed in aqueous medium, leading to leaching out of the mannitol, thereby creating a highly porous internal structure. This porous structure enhances enzymatic processing of encapsulated proteins. After optimizing the conditions to process these microparticles we demonstrate that they strongly enhance cross-presentation in vitro by dendritic cells to CD8 T cells. In vivo experiments in mice confirm that this vaccine formulation technology is capable of enhancing cellular immune responses. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:99 / 109
页数:11
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