Papadopoulos Jordan, Karpouzis Anthony, Tentes John, Kouskoukis Constantin
Department of Dermatology, Faculty of Medicine, Democritus University of Thrace, Greece.
Laboratory of Biochemistry, Faculty of Medicine, Democritus University of Thrace, Greece.
J Clin Med Res. 2014 Apr;6(2):133-7. doi: 10.14740/jocmr1645w. Epub 2014 Feb 6.
Urticaria is a skin disease that affects approximately 5% of the general population and manifests itself, not only as an acute but also as a chronic disease. The etiology of the disease varies as well as its clinical manifestations which extend from the presence of urticarial hives to the potentially mortal angioedema. There is a great interest to the disease not only due to its special clinical manifestation but also due to its pathogenetic mechanism. New data in the medical bibliography support the participation of interleukins (ILs) in the pathophysiology of urticaria. The aim of the study is to contribute in the comprehension of possible participation of certain ILs in the pathogenesis of acute urticaria.
Our study concerns four ILs, IL-4, IL-6, IL-8 and IL-10, simultaneously and their quantitative changes during the acute phase of urticaria as well as 2 weeks after drug administration. Moreover, ILs levels of patients were compared with those of matched healthy controls. All measurements have been done by the ELISA method. The statistical analysis was done by SPSS.
The results present increased levels (in 51 patients vs. 22 matched healthy controls) of all four ILs during the acute phase. Especially for IL-4 this increase was statistically very significant (P < 0.001). Statistically marginally significant decrease was also observed for IL-10 concentrations (P < 0.059), for the two blood samples (acute phase and 2 weeks later).
It is suggested by the present study that certain ILs might play an important role in the pathogenetic mechanism of urticaria. IL-4 and IL-10 participation seems to be relatively more significant. Possibly, ILs, liberated by mast cells, induce an influx of leukocytes in the dermis, therefore participating in the development of acute urticaria inflammation.
荨麻疹是一种皮肤病,影响着约5%的普通人群,不仅表现为急性疾病,也表现为慢性疾病。该疾病的病因各不相同,其临床表现也多种多样,从出现荨麻疹风团到可能致命的血管性水肿。人们对该疾病的兴趣浓厚,不仅因其特殊的临床表现,还因其发病机制。医学文献中的新数据支持白细胞介素(ILs)参与荨麻疹的病理生理学过程。本研究的目的是有助于理解某些白细胞介素在急性荨麻疹发病机制中的可能作用。
我们的研究同时关注四种白细胞介素,即IL-4、IL-6、IL-8和IL-10,以及它们在荨麻疹急性期和药物治疗2周后的定量变化。此外,还将患者的白细胞介素水平与匹配的健康对照组进行了比较。所有测量均采用酶联免疫吸附测定(ELISA)法进行。统计分析采用社会科学统计软件包(SPSS)完成。
结果显示,在急性期,所有四种白细胞介素的水平均升高(51例患者与22例匹配的健康对照组相比)。特别是IL-4的升高在统计学上非常显著(P < 0.001)。对于IL-10浓度,在两个血样(急性期和2周后)中也观察到统计学上的边缘显著下降(P < 0.059)。
本研究表明,某些白细胞介素可能在荨麻疹的发病机制中起重要作用。IL-4和IL-10的参与似乎相对更为显著。可能是肥大细胞释放的白细胞介素诱导白细胞流入真皮,从而参与急性荨麻疹炎症的发展。