Martín A P, Gagliardi J, Baena-Cagnani C E, Eberhard Y, Uguccioni M, Gallino N, Mariani A L, Serra H M
Inmunología, Departamento de Bioquímica Clínica, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Córdoba, Argentina.
Clin Exp Allergy. 2003 Aug;33(8):1118-24. doi: 10.1046/j.1365-2222.2003.01712.x.
Leucocyte migration within inflammatory skin compartments in allergic contact dermatitis (ACD) is the result of a sophisticated multi-step event where multiple molecules are involved.
Since non-antigen-specific mechanisms have been described as an early participant in elicitation of ACD, we investigated the kinetics of the expression of monocyte chemoattractant protein-1 (MCP-1/CCL2) and the type of infiltrating cells. We compared the time course production of MCP-1/CCL2 with connecting segment-1 (CS-1) fibronectin and thymus and activation-regulated chemokine (TARC/ CCL17) expression.
Biopsies from 10 individuals challenged in their back with the antigen responsible for their contact dermatitis and an irrelevant antigen were taken at different times and histology, immunohistochemistry for CS-1 fibronectin, TARC/CCL17, CD3, CD68, CXCR3, CCR4 and in situ hybridization for MCP-1/CCL2 were performed.
At positive antigen stimulated sites expression of MCP-1/CCL2 by basal keratinocytes and isolated cells in dermis started at 10 h. CS-1 fibronectin and TARC/CCL17 expression by blood endothelial cells was found at 2 and 10 h, respectively. This was followed by dermal accumulation of mononuclear cells with a significant increase of CD3+ and CD68+cells. At 48 h, approximately 58% of infiltrating cells were CXCR3+, and 35% CCR4+.
We showed evidence of the fact that CS-1 fibronectin expression precedes the production of MCP-1/CCL2 and TARC/CCL17 in the skin of patients with ACD, suggesting that these molecules participate in the early complex process of migrating mononuclear cells during elicitation of ACD.
在过敏性接触性皮炎(ACD)中,白细胞在炎症性皮肤区域内的迁移是一个复杂的多步骤过程,涉及多种分子。
由于非抗原特异性机制已被描述为引发ACD的早期参与者,我们研究了单核细胞趋化蛋白-1(MCP-1/CCL2)的表达动力学以及浸润细胞的类型。我们比较了MCP-1/CCL2与连接段-1(CS-1)纤连蛋白以及胸腺和活化调节趋化因子(TARC/CCL17)表达的时间进程。
对10名背部用引起其接触性皮炎的抗原和无关抗原进行激发的个体,在不同时间进行活检,并进行组织学检查、CS-1纤连蛋白、TARC/CCL17、CD3、CD68、CXCR3、CCR4的免疫组织化学检查以及MCP-1/CCL2的原位杂交。
在阳性抗原刺激部位,基底角质形成细胞和真皮中分离细胞的MCP-1/CCL2表达在10小时开始。血液内皮细胞的CS-1纤连蛋白和TARC/CCL17表达分别在2小时和10小时被发现。随后是单核细胞在真皮中的积聚,CD3+和CD68+细胞显著增加。在48小时时,约58%的浸润细胞为CXCR3+,35%为CCR4+。
我们证明了在ACD患者皮肤中,CS-1纤连蛋白的表达先于MCP-1/CCL2和TARC/CCL17的产生,这表明这些分子参与了ACD激发过程中单核细胞迁移的早期复杂过程。