Signal transducer and activator of transcription 1 decoy oligodeoxynucleotide suppression of contact hypersensitivity

被引:24
|
作者
Wagner, Andreas H. [1 ]
Wittjen, Inka [1 ]
Stojanovic, Tomislav [2 ]
Middel, Peter [3 ]
Meingassner, Josef G. [4 ]
Hecker, Markus [1 ]
机构
[1] Univ Heidelberg Hosp, Inst Physiol & Pathophysiol, Div Cardiovasc Physiol, D-69120 Heidelberg, Germany
[2] Univ Gottingen, Thoracic & Cardiovasc Surg, Vienna, Austria
[3] Univ Gottingen, Pathol, Vienna, Austria
[4] Novartis Inst Biomed Res, Vienna, Austria
关键词
contact hypersensitivity; allergic contact dermatitis; signal transducer and activator of transcription 1; decoy oligodeoxynucleotide; gene expression;
D O I
10.1016/j.jaci.2007.09.015
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Cytokines play a pivotal role in allergy development through activating signaling mechanisms, such as the Janus kinase/signal transducer and activator of transcription (STAT) pathway, which controls the expression of numerous proinflammatory genes. Objective: In comparison with 2 different corticosteroids and a calcineurin inhibitor, the efficacy of a STAT1 decoy oligodeoxynucleotide (dODN)-containing ointment on hapten-induced contact hypersensitivity was examined in 3 different animal models. Methods: After sensitization, the test compounds were administered before hapten challenge, after hapten challenge, or both to different sites of the animal skin. Subsequent erythema and edema formation was scored macroscopically, microscopically, or by a shift in ear weight. Biopsy specimens were taken and processed for histopathology, immunohistochemistry, and real-time PCR analyses. Results: Treatment with the STAT1 dODN but not the corresponding control ODN markedly improved the clinical signs of inflammation in all 3 animal models in a dose-related manner. In guinea pig skin this was accompanied by a distinct decrease in leukocyte infiltration into the dermis after 24 hours. In addition, expression of CD40, IFN-gamma, IL-1 beta, IL-8, IL-12, and TNF-alpha was strongly attenuated. The dODN was equally effective in the domestic pig model when administered therapeutically, and its preventive effect in the mouse model lasted for more than 48 hours. Conclusions: Altogether, treatment with the dODN proved to be at least as effective as treatment with the reference compounds.
引用
收藏
页码:158 / 165
页数:8
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