The use of Th1 cytokines, IL-12 and IL-23, to modulate the immune response raised to a DNA vaccine delivered by gene gun

被引:22
|
作者
Williman, Jonathan [1 ]
Lockhart, Euan [1 ]
Slobbe, Lynn [1 ]
Buchan, Glenn [1 ]
Baird, Margaret [1 ]
机构
[1] Univ Otago, Dept Microbiol & Immunol, Dunedin, New Zealand
关键词
DNA vaccine; cytokine adjuvant;
D O I
10.1016/j.vaccine.2005.08.011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Unlike intramuscular injection, gene gun delivery of DNA drives a strong type 2 response. In an effort to counter this, we have genetically fused the type 1 cytokines,IL-12 and IL-23, to the hemagglutinin (HA) gene from influenza APR/8/34, and delivered these DNA constructs to Balb/c mice. Gene gun delivery of the HA gene was able to induce antibody production by all vaccinated mice. Linking of IL-12 caused almost complete suppression of immune responses whereas mice vaccinated with IL-23HA showed long-lived IgG1 antibody levels. Splenocytes from IL-23HA vaccinated mice also tended to produce more IL-5 and IFN gamma after restimulation in vitro than splenocytes from HA vaccinated mice. While codelivery of IL-23 did not change the type of immune response it may increase its longevity following vaccination. (c) 2005 Elsevier Ltd. All fights reserved.
引用
收藏
页码:4471 / 4474
页数:4
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