Poly-L-lysine-coated nanoparticles: A potent delivery system to enhance DNA vaccine efficacy

被引:98
作者
Minigo, Gabriela
Scholzen, Anja
Tang, Choon K.
Hanley, Jennifer C.
Kalkanidis, Martha
Pietersz, Geoffrey A.
Apostolopoulos, Vasso
Plebanski, Magdalena
机构
[1] Austin Hosp, Austin Res Inst, Burnet Inst, Vaccine & Infect Dis Lab, Heidelberg, Vic 3084, Australia
[2] Austin Hosp, Austin Res Inst, Burnet Inst, Immunol & Vaccine Lab, Heidelberg, Vic 3084, Australia
[3] Austin Hosp, Austin Res Inst, Burnet Inst, Bioorgan & Med Chem Lab, Heidelberg, Vic 3084, Australia
关键词
nanoparticles; DNA vaccine; ovalbumin; poly-L-lysine; tumour;
D O I
10.1016/j.vaccine.2006.09.086
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
DNA formulations provide the basis for safe and cost efficient vaccines. However, naked plasmid DNA is only poorly immunogenic and new effective delivery strategies are needed to enhance the potency of DNA vaccines. In this study, we present a novel approach for the delivery of DNA vaccines using inert poly-L-lysine (PLL) coated polystyrene particles, which greatly enhance DNA immunogenicity. Intradermal injection of plasmid DNA encoding for chicken egg ovalbumin (OVA) complexed with PLL-coated polystyrene nanoparticles induced high levels of CD8 T cells as well as OVA-specific antibodies in C57BL/6 mice and furthermore inhibited tumour growth after challenge with the OVA expressing EG7 tumour cell line. Importantly, vaccine efficacy depended critically on the size of the particles used as well as on the presence of the PLL linker. Our data show that PLL-coated polystyrene nanoparticles of 0.05 mu m but not 0.02 mu m or 1.0 mu m diameter are highly effective for the delivery of DNA vaccines. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1316 / 1327
页数:12
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