Kemény L, Kenderessy A S, Olasz E, Michel G, Ruzicka T, Farkas B, Dobozy A
Department of Dermatology, Albert Szent-Györgyi Medical University, Szeged, Hungary.
Eur J Pharmacol. 1994 Jun 13;258(3):269-72. doi: 10.1016/0014-2999(94)90490-1.
Interleukin-8 is assumed to play a central role in the pathogenesis of psoriasis. Since an increased expression of the interleukin-8 receptor has been observed both in polymorphonuclear leukocytes and in affected psoriatic epidermis, we were interested in whether the interleukin-8 receptor could be a molecular target of antipsoriatic compounds. Cyclosporine, calcitriol, calcipotriol or dithranol caused a dose-dependent decrease in interleukin-8 binding to cultured human keratinocytes, while interleukin-8 binding to granulocytes was not affected. In addition, the interleukin-8-induced human leukocyte antigen-DR (HLA-DR) expression of keratinocytes was nearly completely blocked by treatment of the cells with these substances. The inhibition of the keratinocyte interleukin-8 receptor and its function by antipsoriatic drugs may contribute to their therapeutic action.
白细胞介素-8被认为在银屑病的发病机制中起核心作用。由于在多形核白细胞和受累的银屑病表皮中均观察到白细胞介素-8受体的表达增加,我们对白细胞介素-8受体是否可能成为抗银屑病化合物的分子靶点感兴趣。环孢素、骨化三醇、卡泊三醇或地蒽酚可使白细胞介素-8与培养的人角质形成细胞的结合呈剂量依赖性降低,而白细胞介素-8与粒细胞的结合不受影响。此外,用这些物质处理细胞几乎完全阻断了白细胞介素-8诱导的角质形成细胞人白细胞抗原-DR(HLA-DR)表达。抗银屑病药物对角质形成细胞白细胞介素-8受体及其功能的抑制作用可能有助于其治疗作用。