YKL-40在扁平地衣组织中的表达

IF 0.3 Q4 DERMATOLOGY
R. Doss, L. Rashed, M. Abdellatif
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引用次数: 0

摘要

背景扁平苔藓(LP)是一种皮肤、粘膜和指甲的特发性慢性炎症性疾病。LP的确切发病机制尚不清楚。几丁质酶-3样蛋白1(YKL-40)是18种糖基水解酶之一,但缺乏酶活性。最近的研究表明,YKL-40存在于炎症和组织重塑部位,触发免疫反应,并吸引嗜酸性粒细胞和T细胞。目的阐明YKL-40在LP炎症中的作用。患者和方法本病例对照研究包括30名皮肤LP患者和30名健康志愿者作为对照。对LP患者的皮肤损伤和对照组的健康皮肤进行了约4mm的穿刺皮肤活检。用聚合酶链式反应技术检测皮肤活组织中YKL-40。结果YKL-40在LP病变中的表达(5.12±1.02 pg/ml)明显高于对照组(1.02±0.05 pg/ml)(P<0.001)。YKL-40的表达与LP类型、病程无显著相关性。结论YKL-40的上调可能在LP的发病机制中发挥作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
YKL-40 tissue expression in lichen planus
Background Lichen planus (LP) is an idiopathic chronic inflammatory disease of the skin, mucous membranes, and nails. The exact pathogenesis of LP is still unclear. Chitinase-3-like protein 1 (YKL-40) is one of the 18 glycosyl hydrolases, but lacks enzymatic activity. Recent studies have shown that YKL-40 is present at sites of inflammation and tissue remodeling, triggers immune responses, and attracts eosinophils and T cells. Objective To clarify a suggested role of YKL-40 in LP inflammation. Patients and methods This case–control study included 30 cutaneous LP patients and 30 healthy volunteers serving as controls. About 4-mm punch-skin biopsies were taken from skin lesions in LP patients and healthy skin from controls. Skin biopsies were examined for YKL-40 using PCR technique. Results The expression of YKL-40 in LP lesions (5.12±1.02 pg/ml) was significantly higher than their expression in control-tissue biopsies (1.02±0.05 pg/ml) (P<0.001). No significant relation was detected between the expression of YKL-40, type of LP, and the disease duration. Conclusion We can conclude that upregulation of YKL-40 could point to a possible role in the pathogenesis of LP.
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来源期刊
CiteScore
0.50
自引率
0.00%
发文量
0
审稿时长
17 weeks
期刊介绍: The Journal of The Egyptian Women''s Dermatologic Society (JEWDS) was founded by Professor Zenab M.G. El-Gothamy. JEWDS is published three times per year in January, May and September. Original articles, case reports, correspondence and review articles submitted for publication must be original and must not have been published previously or considered for publication elsewhere. Their subject should pertain to dermatology or a related scientific and technical subject within the field of dermatology.
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