Schröder J M
Department of Dermatology, University of Kiel, Federal Republic of Germany.
Arch Dermatol Res. 1992;284 Suppl 1:S22-6. doi: 10.1007/BF00638236.
In the last decade a number of proteinaceous inflammatory mediators have been structurally characterized. Two of these mediators, tumor necrosis factor alpha (TNF alpha) and Interleukin 1 alpha and beta (IL-1), have pleiotropic properties. Both cytokines are now known to be potent inducers of a number of cell-selective chemotactic cytokines, which belong to a novel superfamily of structurally related low-molecular-weight proteins. One of the most prominent members is termed "IL-8" and represents a neutrophil-selective attractant, whereas another one called "monocyte chemotactic protein 1 (MCP-1)" is a monocyte-selective chemotaxin. Other members seem to be selective chemotaxins for other leukocyte types and subsets. These chemotactic cytokines are produced by a variety of different cells under appropriate stimulation conditions. Large amounts of IL-8 have been detected in scales of psoriatic lesions and may be of importance in explaining predominant neutrophil infiltration in psoriatic lesions. Regulation of gene expression and/or release of these chemotactic cytokines may occur by IL-1 receptor antagonists or soluble TNF-alpha-receptors. So far, natural antagonists to these chemotactic cytokines have not been described; however, pharmacological inhibition of its gene expression and/or release is possible.
在过去十年中,一些蛋白质类炎症介质的结构已被阐明。其中两种介质,肿瘤坏死因子α(TNFα)和白细胞介素1α及β(IL-1),具有多效性。现在已知这两种细胞因子都是多种细胞选择性趋化因子的强效诱导剂,这些趋化因子属于一个结构相关的低分子量蛋白质的新型超家族。最突出的成员之一被称为“IL-8”,是一种中性粒细胞选择性吸引剂,而另一种称为“单核细胞趋化蛋白1(MCP-1)”的则是单核细胞选择性趋化因子。其他成员似乎是针对其他白细胞类型和亚群的选择性趋化因子。这些趋化因子在适当的刺激条件下由多种不同细胞产生。在银屑病皮损鳞屑中已检测到大量IL-8,这可能对解释银屑病皮损中主要的中性粒细胞浸润具有重要意义。这些趋化因子的基因表达和/或释放的调节可能通过IL-1受体拮抗剂或可溶性TNF-α受体来实现。到目前为止,尚未描述这些趋化因子的天然拮抗剂;然而,对其基因表达和/或释放进行药理学抑制是可能的。