Martín Andrea, Gallino Norberto, Gagliardi Julio, Ortiz Susana, Lascano Alejandro Ruiz, Diller Ana, Daraio María Cristina, Kahn Adrián, Mariani Ana Lía, Serra Horacio Marcelo
Dpto Bioquímica Clínica, Facultad de Ciencias Químicas-Universidad Nacional de Córdoba, Córdoba, Argentina.
BMC Dermatol. 2002 Aug 7;2:9. doi: 10.1186/1471-5945-2-9.
Allergic Contact Dermatitis (ACD) is regarded as a T-cell-mediated delayed-type hypersensitivity reaction. We studied the kinetics of the expression of CS-1 fibronectin, thymus and activation-regulated chemokine (CCL17/ TARC) and different chemokine receptors (CR) in skin biopsies from individuals suffering from back problems, with the antigen responsible of their contact dermatitis and an irrelevant antigen.
Samples were taken at 2, 10, and 48 hours for histological and immunohistochemical studies using monoclonal antibodies against human CS-1 fibronectin, CCL17, CD3, CD68, CD49d, CXCR3, CCR5, and CCR3.
At positive antigen stimulated sites there was an early expression of CS-1 fibronectin (2 hours), followed by CCL17 and a later accumulation of alplha4/beta1+ (CD49d), CD3+, CD68+, CXCR3+ and CCR5+ mononuclear cells. At 48 hours, approximately 59 % of infiltrating cells were CXCR3+, 42% CCR5+, and only 14 % CCR3+.
These results showed for the first time a very early expression of CS-1 fibronectin which preceded production of CCL17 in blood endothelial cells (BCEs) from patients' skin with ACD. The role of these molecules in recruitment of monocytes and effector T cells in ACD is discussed.
过敏性接触性皮炎(ACD)被认为是一种T细胞介导的迟发型超敏反应。我们研究了患有背部问题的个体皮肤活检中CS-1纤连蛋白、胸腺和活化调节趋化因子(CCL17/TARC)以及不同趋化因子受体(CR)的表达动力学,这些个体接触了导致其接触性皮炎的抗原以及一种无关抗原。
在2小时、10小时和48小时采集样本,用于组织学和免疫组织化学研究,使用针对人CS-1纤连蛋白、CCL17、CD3、CD68、CD49d、CXCR3、CCR5和CCR3的单克隆抗体。
在阳性抗原刺激部位,CS-1纤连蛋白早期表达(2小时),随后是CCL17表达,以及α4/β1+(CD49d)、CD3+、CD68+、CXCR3+和CCR5+单核细胞的后期聚集。在48小时时,约59%的浸润细胞为CXCR3+,42%为CCR5+,只有14%为CCR3+。
这些结果首次显示,在患有ACD的患者皮肤的血管内皮细胞(BCEs)中,CS-1纤连蛋白的表达非常早,先于CCL17的产生。讨论了这些分子在ACD中单核细胞和效应T细胞募集中的作用。