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用于预测局部用药疗效的过敏性接触性皮炎激发后模型。

Postelicitation model of allergic contact dermatitis for predicting the efficacy of topical drugs.

作者信息

Kammeyer Arthur, Bos Jan D, Teunissen Marcel B M

机构信息

Department of Dermatology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.

出版信息

Exp Dermatol. 2009 Jan;18(1):44-9. doi: 10.1111/j.1600-0625.2008.00757.x. Epub 2008 Oct 22.

DOI:10.1111/j.1600-0625.2008.00757.x
PMID:19054064
Abstract

To evaluate the anti-inflammatory efficacies of topical drugs, models of contact hypersensitivity (CHS) can be used, but the conventional murine models of CHS need revision in this respect. These models utilize sensitized mice to study suppression of sensitization or elicitation by test compounds. To mimick the events occurring in allergic contact dermatitis (ACD), a modification of the murine model of CHS is needed in a way that a chronic postelicitation phase of CHS is maintained for studies of anti-inflammatory effects of topical drugs, typically relevant for ACD therapy, not for ACD prevention. A method for the quantification of the suppression of ACD by a test compound is presented here. Two experimental drugs for topical use, imidazole-4-carboxylate and imidazole-4-acetate, were tested in parallel with the corticosteroid prednisolone. We found that prednisolone showed strong suppressive effects, while imidazole-4-carboxylate and imidazole-4-acetate showed mild suppressive effects during persistent ACD simulation. Multiple elicitations on the mouse ears led to scratching and the formation of abrasions and scabbings with, presumably, worsening of discomfort. Clear reduction of these side-phenomena was achieved by tailoring the topical amount of contact sensitizer, while the ability of the ACD model to test anti-inflammatory compounds, was not affected. By focussing on a prolonged postelicitation phase of CHS, a simulation of ACD has been established. We demonstrated that this model may provide an improved predictability for the clinical efficacies of (experimental) mild or strong anti-inflammatory drugs.

摘要

为评估局部用药的抗炎效果,可采用接触性超敏反应(CHS)模型,但传统的小鼠CHS模型在这方面需要改进。这些模型利用致敏小鼠来研究受试化合物对致敏或激发的抑制作用。为模拟变应性接触性皮炎(ACD)中发生的事件,需要对小鼠CHS模型进行改进,以便维持CHS激发后的慢性阶段,用于研究局部用药的抗炎作用,这通常与ACD治疗相关,而非ACD预防。本文介绍了一种定量测试化合物对ACD抑制作用的方法。将两种局部用实验药物咪唑-4-羧酸盐和咪唑-4-乙酸盐与皮质类固醇泼尼松龙并行测试。我们发现,在持续模拟ACD期间,泼尼松龙显示出强烈的抑制作用,而咪唑-4-羧酸盐和咪唑-4-乙酸盐显示出轻微的抑制作用。对小鼠耳部进行多次激发会导致抓挠以及擦伤和结痂的形成,这可能会使不适感加剧。通过调整接触性致敏剂的局部用量,这些副作用现象明显减轻,而ACD模型测试抗炎化合物的能力未受影响。通过关注CHS激发后的延长阶段,建立了ACD模拟模型。我们证明,该模型可为(实验性)轻度或强效抗炎药物的临床疗效提供更好的预测。

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