Broegelmann Research Laboratory, Department of Clinical Science, University of Bergen, Bergen, Norway.
Department of Dermatology, Haukeland University Hospital, Bergen, Norway.
Scand J Immunol. 2018 Dec;88(6):e12725. doi: 10.1111/sji.12725. Epub 2018 Nov 4.
Psoriasis is an immune-mediated disease where the IL-23/Th17 axis as well as TNF comprise main targets of biological therapy. Immune profiling has so far not been embraced as a clinical tool. We aimed to investigate relationships between individual serum cytokine levels in 40 psoriasis patients before and after receiving biological therapy and Psoriasis Area and Severity Index (PASI) and Dermatological Life Quality Index (DLQI). Serum concentration of 25 cytokines was determined by Luminex technology. Mean PASI and DLQI decreased by 71% and 65%, respectively. Increase of IL-2 positively correlated with improvement of PASI and DLQI. Moreover, increase of IL-5, IL-10, IL-12, IL-22 and GM-CSF correlated with treatment effect. Notably, logistic regression revealed four times higher risk of having severe psoriasis when IL-17A increased by 1 pg/mL (OR: 4.06, P < 0.05). Selected serum cytokines might constitute useful biomarkers for monitoring disease activity and optimizing therapeutic strategies in psoriasis patients.
银屑病是一种免疫介导的疾病,IL-23/Th17 轴和 TNF 是生物治疗的主要靶点。免疫分析迄今为止尚未被用作临床工具。我们旨在研究 40 例接受生物治疗前后银屑病患者个体血清细胞因子水平与银屑病面积和严重程度指数(PASI)和皮肤病生活质量指数(DLQI)之间的关系。通过 Luminex 技术测定 25 种细胞因子的血清浓度。平均 PASI 和 DLQI 分别降低了 71%和 65%。IL-2 的增加与 PASI 和 DLQI 的改善呈正相关。此外,IL-5、IL-10、IL-12、IL-22 和 GM-CSF 的增加与治疗效果相关。值得注意的是,逻辑回归显示当 IL-17A 增加 1 pg/mL 时,发生严重银屑病的风险增加四倍(OR:4.06,P<0.05)。选定的血清细胞因子可能构成监测疾病活动和优化银屑病患者治疗策略的有用生物标志物。