Rapid kinetics to peak serum antibodies is achieved following influenza vaccination by dry-coated densely packed microprojections to skin

被引:31
作者
Chen, Xianfeng [1 ]
Fernando, Germain J. P. [1 ]
Raphael, Anthony P. [1 ]
Yukiko, Sally R. [1 ]
Fairmaid, Emily J. [2 ]
Primiero, Clare A. [1 ]
Frazer, Ian H. [3 ]
Brown, Lorena E. [2 ]
Kendall, Mark A. F. [1 ,3 ]
机构
[1] Univ Queensland, Australian Inst Bioengn & Nanotechnol, Delivery Drugs & Genes Grp D2G2, Brisbane, Qld 4072, Australia
[2] Univ Melbourne, Dept Microbiol & Immunol, Parkville, Vic 3010, Australia
[3] Univ Queensland, Diamantina Inst, Brisbane, Qld 4102, Australia
基金
比尔及梅琳达.盖茨基金会; 英国医学研究理事会; 澳大利亚研究理事会;
关键词
Microprojections; Microneedles; Skin delivery; Needle free vaccination; VIRUS-LIKE PARTICLES; MICRONEEDLE DELIVERY; IMMUNIZATION; ARRAYS; PROTECTION; MICE; TIME; CHALLENGE; PATCHES;
D O I
10.1016/j.jconrel.2011.10.026
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A rapid time to peak serum antibody response following vaccination is particularly important for influenza: the time window between the availability of appropriate antigen and the start of the seasonal epidemic is very short. In this paper, influenza vaccine was delivered to both the epidermis and dermis of mouse skin using densely packed microprojection arrays for vaccination. We found that, after vaccination, around 75% and 90% of the delivered influenza vaccine migrated away from the ear skin within just 2 days and 1 week - respectively. And the time to peak serum antibody response was as early as 2 weeks. This result matches the kinetics achieved by intramuscular injection of liquid vaccine to muscle. Thus, we demonstrate that skin delivery of small vaccine volumes discretely by thousands of densely packed microprojections neither induces delay in kinetics nor interferes with the long-lasting antibody response; compared to conventional intramuscular injection. (c) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:78 / 84
页数:7
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