Szczepanik-Kułak Paulina, Michalska-Jakubus Małgorzata, Kowal Małgorzata, Krasowska Dorota
Chair and Department of Dermatology, Venerology and Paediatric Dermatology, Medical University of Lublin, 20-081 Lublin, Poland.
J Clin Med. 2022 Oct 28;11(21):6375. doi: 10.3390/jcm11216375.
Morphea/localized scleroderma (LoS) represents an inflammatory-sclerotic skin disease, the pathogenesis of which is not fully understood. Given the important role of IL-1 family cytokines in the development and therapy of inflammatory diseases, including systemic sclerosis, we analyzed the clinical significance of serum levels of selected IL-1 family cytokines (IL-1α, IL-1β, IL-18, IL-33, IL-37 and IL-38) in LoS patients (n = 30) using the standardized disease assessment tools and comparison to healthy controls (n = 28). We also compared the pre- and post-treatment concentrations, i.e., before and after systemic (glucocorticosteroids and/or methotrexate) and/or topical (topical glucocorticosteroids and/or calcineurin inhibitors). Our findings did not reveal significant differences in baseline IL-1α, IL-1β, IL-18, IL-33, IL-37 and IL-38 levels between LoS group and HCs; however, after treatment, there were marked changes in concentrations of IL-1α and IL-33 within LoS group as well as in comparison to HCs. We also found significant negative correlations between PGA-A and IL-1α concentration as well as between mLoSSI and IL-1α after treatment. Furthermore, we showed an inverse correlation of baseline IL-1β levels with mLoSSI scores of borderline significance. We believe that IL-1α and IL-33, as well as Il-1β, may be potential mediators and targets of interest in LoS.
硬斑病/局限性硬皮病(LoS)是一种炎症性硬化性皮肤病,其发病机制尚未完全明确。鉴于白细胞介素-1(IL-1)家族细胞因子在包括系统性硬化症在内的炎症性疾病的发生发展及治疗中发挥重要作用,我们使用标准化疾病评估工具,分析了LoS患者(n = 30)血清中选定的IL-1家族细胞因子(IL-1α、IL-1β、IL-18、IL-33、IL-37和IL-38)水平的临床意义,并与健康对照者(n = 28)进行比较。我们还比较了治疗前后的浓度,即全身治疗(糖皮质激素和/或甲氨蝶呤)和/或局部治疗(局部糖皮质激素和/或钙调神经磷酸酶抑制剂)前后的浓度。我们的研究结果显示,LoS组与健康对照组之间,基线时IL-1α、IL-1β、IL-18、IL-33、IL-37和IL-38水平无显著差异;然而,治疗后,LoS组内以及与健康对照组相比,IL-1α和IL-33的浓度有明显变化。我们还发现,治疗后医师全面评估(PGA-A)与IL-1α浓度之间以及改良局限性硬皮病严重程度指数(mLoSSI)与IL-1α之间存在显著负相关。此外,我们发现基线IL-1β水平与mLoSSI评分之间存在临界显著性的负相关。我们认为,IL-1α、IL-33以及IL-1β可能是LoS潜在的介质和研究靶点。