Olejniczak-Staruch Irmina, Narbutt Joanna, Bednarski Igor, Woźniacka Anna, Sieniawska Joanna, Kraska-Gacka Marzena, Śmigielski Janusz, Lesiak Aleksandra
Department of Dermatology and Venereology, Medical University of Lodz, Lodz, Poland.
Department of Dermatology, Pediatric Dermatology and Dermatological Oncology, Medical University of Lodz, Lodz, Poland.
Postepy Dermatol Alergol. 2020 Oct;37(5):705-711. doi: 10.5114/ada.2020.100481. Epub 2020 Nov 7.
Psoriasis, affecting approximately 2% of the worldwide population, is a chronic, inflammatory skin disease in which overexpression of proinflammatory cytokines is observed. Most of the available data on the influence of antipsoriatic therapy on the cytokine serum concentration are inconsistent and based on short-term observations.
To evaluate the influence of long-term biologic therapy with tumor necrosis factor α (TNF-α) blockers (adalimumab, etanercept, infliximab) and IL-12/23 inhibitor (ustekinumab) on the level of IL-6, IL-22 in the sera of patients with psoriasis.
Blood samples were collected from 42 psoriatic patients in order to determine IL-6 and IL-22 serum concentrations prior to and at the 3, 12, 24 and 36 month of biologic therapy. Psoriasis Activity and Severity Index (PASI) was assessed at the same time points. The control group consisted of 30 sex- and age-matched healthy volunteers.
Mean PASI index at baseline was 14.49 ±3.69 and decreased significantly until the end of the observation. Mean IL-6 serum concentration decreased significantly in all study groups ( < 0.05). A statistically significant decrease in IL-22 concentrations was demonstrated during the treatment with adalimumab and infliximab but not etanercept or ustekinumab.
According to obtained results, IL-6 and IL-22 serum concentration may be an accurate marker of response to antipsoriatic therapy, even though not correlated with PASI index. Biologic therapy in psoriasis allows for long-term clinical improvement expressed not only by the remission of skin lesions, but also by lowering serum concentrations of pro-inflammatory interleukins.
银屑病影响着全球约2%的人口,是一种慢性炎症性皮肤病,其中促炎细胞因子会过度表达。关于抗银屑病疗法对细胞因子血清浓度影响的现有数据大多不一致,且基于短期观察。
评估长期使用肿瘤坏死因子α(TNF-α)阻滞剂(阿达木单抗、依那西普、英夫利昔单抗)和白细胞介素-12/23抑制剂(乌司奴单抗)进行生物治疗对银屑病患者血清中白细胞介素-6(IL-6)、白细胞介素-22(IL-22)水平的影响。
采集42例银屑病患者的血样,以测定生物治疗前及治疗3、12、24和36个月时的IL-6和IL-22血清浓度。同时在相同时间点评估银屑病活动和严重程度指数(PASI)。对照组由30名年龄和性别匹配的健康志愿者组成。
基线时的平均PASI指数为14.49±3.69,至观察结束时显著下降。所有研究组的平均IL-6血清浓度均显著降低(<0.05)。在使用阿达木单抗和英夫利昔单抗治疗期间,IL-22浓度有统计学意义的下降,但依那西普或乌司奴单抗治疗期间未出现此情况。
根据所得结果,IL-6和IL-22血清浓度可能是抗银屑病治疗反应的准确标志物,尽管与PASI指数无关。银屑病的生物治疗不仅能使皮肤病变缓解,还能降低促炎白细胞介素的血清浓度,从而实现长期临床改善。