Hayran Yıldız, Yücel Çiğdem, Oğuz Esra Fırat, Eren Funda, Turhan Turan, Yalçın Başak
Department of Dermatology, Ankara City Hospital, Ankara, Turkey.
Department of Medical Biochemistry, University of Health Sciences, Gulhane Teaching and Research Hospital, Ankara, Turkey.
Dermatol Pract Concept. 2024 Apr 1;14(2):e2024069. doi: 10.5826/dpc.1402a69.
Vitiligo is a chronic skin disorder in which immune dysregulation has been reported as one of the major etiopathological factors. Interleukin-12 (IL-12), IL-23 and IL-27 of IL-12 cytokine family were identified as critical cytokines in the pathogenesis of many autoimmune and inflammatory skin diseases including vitiligo. IL-35 is one of the newest member of IL-12 cytokine family.
The purpose of our study was to examine serum IL-35 levels in addition to serum IL-12, IL-23, IL-27 levels in the vitiligo patients and control group, and to investigate the relationship of these cytokines with the characteristics of vitiligo.
Serum IL-12, IL-23, IL-27 and IL-35 levels of 87 vitiligo patients and 70 healthy volunteers were analyzed using the enzyme-linked immunosorbent assay (ELISA). We compared the IL-12 cytokine family levels in the patient and control groups, and investigated the relationship of these levels with the characteristics of vitiligo.
Patients had higher levels of IL-12 (31.2 versus 20.1, P < 0.001) and IL-35 (9.6 versus 8.1, P = 0.031). Patient and control groups had similar levels of IL-23 (P = 0.78) but were correlated with the Vitiligo Area Scoring Index (VASI) (P = 0.022, r = 0.35). Patients had lower levels of IL-27 (207.6 versus 258.7, P < 0.001). In addition, the levels of serum IL-27 were correlated negatively with the Vitiligo Disease Activity (VIDA), and positively with disease duration (P = 0.007, r = 0.30).
Differences of serum levels between Vitiligo patients and healthy controls, significant relationships with the characteristics of vitiligo suggest that the IL-12 cytokine family may play a role in the pathogenesis of vitiligo.
白癜风是一种慢性皮肤病,免疫失调被认为是主要的病因病理因素之一。白细胞介素12(IL-12)细胞因子家族中的白细胞介素12(IL-12)、白细胞介素23(IL-23)和白细胞介素27(IL-27)被确定为包括白癜风在内的许多自身免疫性和炎症性皮肤病发病机制中的关键细胞因子。白细胞介素35(IL-35)是IL-12细胞因子家族的最新成员之一。
我们研究的目的是检测白癜风患者和对照组血清中IL-35水平以及血清IL-12、IL-23、IL-27水平,并研究这些细胞因子与白癜风特征之间的关系。
采用酶联免疫吸附测定(ELISA)法分析87例白癜风患者和70名健康志愿者血清中IL-12、IL-23、IL-27和IL-35水平。我们比较了患者组和对照组中IL-12细胞因子家族水平,并研究了这些水平与白癜风特征之间的关系。
患者的IL-12水平较高(31.2对20.1,P<0.001)和IL-35水平较高(9.6对8.1,P = 0.031)。患者组和对照组的IL-23水平相似(P = 0.78),但与白癜风面积评分指数(VASI)相关(P = 0.022,r = 0.35)。患者的IL-27水平较低(207.6对258.7,P<0.001)。此外,血清IL-27水平与白癜风疾病活动度(VIDA)呈负相关,与病程呈正相关(P = 0.007,r = 0.30)。
白癜风患者与健康对照者血清水平存在差异,且与白癜风特征有显著关系,提示IL-12细胞因子家族可能在白癜风发病机制中起作用。