Homey B, Schuppe H C, Assmann T, Vohr H W, Lauerma A I, Ruzicka T, Lehmann P
Department of Dermatology, Heinrich Heine University, Düsseldorf, Germany.
Eur J Pharmacol. 1997 May 1;325(2-3):199-207. doi: 10.1016/s0014-2999(97)00116-7.
Topical glucocorticosteroids represent the mainstay of antiinflammatory therapy in the treatment of inflammatory skin diseases. Their clinical use, however, is limited by local and systemic side-effects. Thus, in dermatopharmacology there is a large demand for alternative non-steroidal antiinflammatories. Other than transplantation models, most of the frequently used in vivo test systems for assessment of drug-induced immunosuppression measure changes in inflammatory skin responses by means of skin erythema and edema after challenge of sensitized animals. The aim of this study was to develop an alternative mouse model to detect and analyse immunosuppressive effects of topically applied drugs. On the basis of a modified local lymph node assay, we analysed effects of topical hydrocortisone, dexamethasone, mometasone furoate and FK506 (tacrolimus) during the induction phase of contact hypersensitivity. On 4 consecutive days, NMRI mice were treated on the dorsal surfaces of both ears with increasing concentrations of test compound. During the last 3 days, the mice received in addition the contact sensitizer, oxazolone (1%). On day 5, draining auricular lymph nodes were removed in order to assess lymph node cell counts and perform flow cytometric analysis of lymph node cell subpopulations (CD4+/CD25+, Ia+/CD69+, Ia+/B220+). All test compounds proved to exert significant immunosuppressive effects after topical application, but showed differences in their immunomodulatory potential. In conclusion, the local lymph node assay serves as an appropriate model to characterize immunosuppressive effects of topically applied drugs by measuring immunologically relevant end-points.
局部糖皮质激素是治疗炎症性皮肤病抗炎治疗的主要手段。然而,它们的临床应用受到局部和全身副作用的限制。因此,在皮肤药理学中,对替代性非甾体抗炎药有很大的需求。除了移植模型外,大多数常用的体内测试系统用于评估药物诱导的免疫抑制,通过对致敏动物进行激发后测量皮肤红斑和水肿来检测炎症性皮肤反应的变化。本研究的目的是开发一种替代性小鼠模型,以检测和分析局部应用药物的免疫抑制作用。基于改良的局部淋巴结试验,我们分析了局部应用氢化可的松、地塞米松、糠酸莫米松和FK506(他克莫司)在接触性超敏反应诱导期的作用。连续4天,用浓度递增的受试化合物处理NMRI小鼠双耳的背表面。在最后3天,小鼠还接受接触致敏剂恶唑酮(1%)。在第5天,切除引流耳淋巴结以评估淋巴结细胞计数并对淋巴结细胞亚群(CD4+/CD25+、Ia+/CD69+、Ia+/B220+)进行流式细胞术分析。所有受试化合物经局部应用后均显示出显著的免疫抑制作用,但在免疫调节潜能方面存在差异。总之,局部淋巴结试验通过测量免疫学相关终点,是表征局部应用药物免疫抑制作用的合适模型。