Nickoloff B J, Griffiths E M
Department of Pathology, University of Michigan Medical School, Ann Arbor 48109-0602.
J Invest Dermatol. 1990 Dec;95(6 Suppl):128S-131S. doi: 10.1111/1523-1747.ep12875018.
Because of the identification and characterization of various adhesion molecules (lymphocyte function associated antigen-1, intercellular adhesion molecule-1), chemotactic factors (interleukin-8, monocyte chemotactic/activating factor), and their modulatory cytokines (gamma interferon, tumor necrosis factor), it is possible to begin to ascribe specific molecules to cutaneous cellular reaction patterns. The abnormal topobiology, or altered spatial distribution, of mononuclear cells, which gives rise to disease-specific patterns, was described in molecular terms. A large number of diverse skin diseases were classified into six different groups, with each group highlighting distinctive cell types, adhesion molecules, chemotactic factors, and cytokines. The diseases within each group, which share functional anatomical reaction zones, were postulated to share common pathophysiologic pathways. Thus, it is now possible, as one scans the microscopic field, to look past the static images of red- and blue-stained cells and appreciate a dynamic and detailed medley of molecularly defined events emanating from the eyepiece.
由于各种黏附分子(淋巴细胞功能相关抗原-1、细胞间黏附分子-1)、趋化因子(白细胞介素-8、单核细胞趋化/激活因子)及其调节性细胞因子(γ干扰素、肿瘤坏死因子)的鉴定和特性描述,现在有可能开始将特定分子与皮肤细胞反应模式联系起来。单核细胞的异常拓扑生物学,即空间分布改变,产生了疾病特异性模式,这已从分子层面进行了描述。大量不同的皮肤病被分为六个不同的组,每组突出显示独特的细胞类型、黏附分子、趋化因子和细胞因子。假定每组内具有共同功能解剖反应区的疾病共享共同的病理生理途径。因此,现在当人们在显微镜视野中观察时,就有可能透过红色和蓝色染色细胞的静态图像,领略目镜中分子定义的动态而详细的混合事件。