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Site-Specific Analysis of Inflammatory Markers in Discoid Lupus Erythematosus Skin

机译:肉斑两次红斑狼疮皮肤炎症标志物的特异性分析

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Prior studies identified T cells, B cells, and macrophages in the inflammatory infiltrate and up-regulation of their protein products in discoid lupus erythematosus (DLE) skin; however, they lacked rigorous analyses to define their specific locations in skin. Thus, we compared expressions of selected T cell, B cell, and macrophage markers in five areas of DLE, psoriasis, and normal skin. Immunostainings for CD3, CD4, CD8, CD20, CD68, CXCR3, CXCL10, and TIA-1 were performed in biopsies of 23 DLE lesional skin, 11 psoriasis lesional skin, and 5 normal skin. Three independent observers used a graded scale to rate each marker’s presence in the epidermis, dermatoepidermal junction (DEJ), perivascular area, periadnexal area, and deep dermis. DLE lesional skin contained an increased abundance of CD3+, CD8+, and CD68+cells at the DEJ, and CD20+and CD68+cells in the periadnexal area versus psoriasis and normal skin. CXCR3, CXCL10, and TIA-1 were elevated in periadnexal sites of DLE lesional skin versus psoriasis lesional skin. The aggregation of T cells, B cells, macrophages, and their protein products (CXCR3, CXCL10, and TIA-1) in the DEJ and periadnexal area of DLE lesional skin may contribute to the pathology of DLE through a coordinated, sophisticated process.
机译:先前的研究确定了炎症浸润的T细胞,B细胞和巨噬细胞,在盘状狼疮(DLE)皮肤上的蛋白质产品的上调和上调它们;然而,它们缺乏严格的分析来定义其皮肤的特定位置。因此,我们将所选择的T细胞,B细胞和巨噬细胞标记的表达进行比较在DLE,牛皮癣和正常皮肤的五个区域中。在23个DLE损伤皮肤,11个牛皮癣障碍皮肤和5个正常皮肤的活组织检查中进行CD3,CD4,CD8,CD20,CD68,CXCR3,CXCL10和TIA-1的免疫抑制。三个独立的观察者使用分级规模来评分每种标记在表皮,皮肤病的存在,皮肤病,围嘴巴,植物区,植物区域和深层深层存在。 DLE损伤皮肤在DEJ的CD3 +,CD8 +和CD68 +细胞中含有增加的丰富度,CD20 +和CD68 +细胞,在PeriaDnexal区域与牛皮癣和正常皮肤。 CXCR3,CXCL10和TIA-1升高在DLE障碍皮肤的PeriaDnexal位点与牛皮癣障碍皮肤。 DEJ和PeriaDnexal面积的T细胞,B细胞,巨噬细胞和其蛋白质产品(CXCR3,CXCL10和TIA-1)的聚集可能会通过协调,复杂的过程有助于DLE的病理学。

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