U.O.C. Clinica Dermatologica Dipartimento di Medicina Interna e Specialità Mediciane University of Rome "Sapeinza", Italy.
Int J Immunopathol Pharmacol. 2012 Jul-Sep;25(3):781-8. doi: 10.1177/039463201202500327.
Alopecia areata (AA) has been represented as a restricted T cell-mediated autoimmune disease. Several studies have shown that cytokines may play an important role in its pathogenesis although many pathways exist. We investigated cytokine (IL-2, IL-6, IL-12, and TNFα) levels in peripheral blood mononuclear cell (PBMC) of 105 patients with different grade and duration of alopecia areata, to confirm that T-cell responses in AA is regulated via mechanisms of peripheral T-cell tolerance. We observed that IL-12 levels are higher for patients with bigger extensions and tend to increase according to the duration of the AA; TNFα instead, is more related to the gender of the patients and to the duration. Therefore abnormalities in cytokines production, showed by our results, may suggest that T-cell responses in AA scalp are closely regulated via mechanisms of peripheral T-cell tolerance and therefore confirm that this disease has an immuno-pathogenesis. Our aim is to shed light upon the complexity of AA underlying mechanisms and indicate pathways that may suggest future treatments.
斑秃(AA)被认为是一种局限的 T 细胞介导的自身免疫性疾病。尽管存在许多途径,但已有多项研究表明细胞因子可能在其发病机制中发挥重要作用。我们研究了 105 例不同等级和持续时间的斑秃患者外周血单个核细胞(PBMC)中的细胞因子(IL-2、IL-6、IL-12 和 TNFα)水平,以证实 AA 中的 T 细胞反应是通过外周 T 细胞耐受的机制来调节的。我们观察到,IL-12 水平在扩展较大的患者中较高,并随着 AA 持续时间的延长而增加;相反,TNFα与患者的性别和持续时间更相关。因此,我们的研究结果表明细胞因子产生的异常可能表明 AA 头皮中的 T 细胞反应是通过外周 T 细胞耐受的机制来紧密调节的,从而证实这种疾病具有免疫发病机制。我们的目的是阐明 AA 潜在机制的复杂性,并指出可能提示未来治疗方法的途径。