Tomaszewska Katarzyna A, Kozłowska Magdalena, Kaszuba Andrzej, Lesiak Aleksandra, Narbutt Joanna, Zalewska-Janowska Anna M
Psychodermatology Department, Pulmonology, Rheumatology and Clinical Immunology Chair, Medical University of Lodz, Lodz, Poland.
Department of Dermatology, Pediatric Dermatology and Oncology, Medical University of Lodz, Lodz, Poland.
Postepy Dermatol Alergol. 2022 Feb;39(1):195-199. doi: 10.5114/ada.2022.113612. Epub 2022 Feb 28.
Alopecia areata (AA) and vitiligo are both skin diseases of autoimmune origin. AA is characterized by patchy hair loss primarily on the scalp but may involve other areas as well, while vitiligo is caused by the destruction of melanocytes and results in the appearance of white patches on any part of the body. Many facts indicate similar pathogenesis of these diseases. Both dermatoses are associated with frequent coexistence of other autoimmune diseases and share common genetic risk factors. Recent data support the theory of the involvement of IL-17 in the pathogenesis of both AA and vitiligo.
To evaluate and compare the serum levels of interleukin (IL)-17 in patients with AA and non-segmental vitiligo (NSV). To assess whether the pattern of serum cytokine concentration can be associated with clinical details and activity of the disease.
A cross-sectional study was conducted on 33 patients with AA, 30 patients with NSV, and 30 healthy controls. Serum levels of IL-17 were determined quantitatively by ELISA method.
Our analysis identified a systemic inflammatory signature associated with AA and NSV, characterized by elevated levels of IL-17. The levels of IL-17 did not differ significantly between AA patients and NSV patients.
Our results show that AA and vitiligo may share common etiopathogenetic pathways, which suggests the potential of developing targeted therapies for both AA and vitiligo treatment. Imbalance of T cell subpopulations and complex systemic cytokine profiles may contribute to the pathogenesis of AA and vitiligo.
斑秃(AA)和白癜风均为自身免疫性起源的皮肤病。斑秃的特征是主要在头皮出现斑片状脱发,但也可能累及其他部位,而白癜风是由黑素细胞破坏引起的,导致身体任何部位出现白色斑块。许多事实表明这些疾病的发病机制相似。这两种皮肤病都常与其他自身免疫性疾病共存,并共享常见的遗传风险因素。最近的数据支持白细胞介素-17(IL-17)参与斑秃和白癜风发病机制的理论。
评估和比较斑秃患者与非节段性白癜风(NSV)患者血清中白细胞介素(IL)-17的水平。评估血清细胞因子浓度模式是否与疾病的临床细节和活动相关。
对33例斑秃患者、30例NSV患者和30例健康对照进行了横断面研究。采用酶联免疫吸附测定(ELISA)法定量测定血清IL-17水平。
我们的分析确定了一种与斑秃和NSV相关的全身炎症特征,其特点是IL-17水平升高。斑秃患者和NSV患者的IL-17水平无显著差异。
我们的结果表明,斑秃和白癜风可能共享共同的病因发病途径,这提示了开发针对斑秃和白癜风治疗的靶向疗法的潜力。T细胞亚群失衡和复杂的全身细胞因子谱可能有助于斑秃和白癜风的发病机制。