Shen Zhengyu, Gao Xing, Ma Liwei, Zhou Zengtong, Shen Xuemin, Liu Wei
Department of Dermatology, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, 639 Zhizaoju Road, Shanghai, 200011, China.
Arch Dermatol Res. 2014 Jul;306(5):441-6. doi: 10.1007/s00403-013-1429-3. Epub 2013 Nov 29.
Foxp3 is a specific marker for regulatory T cells (Tregs), and interleukin (IL)-17 is the signature cytokine of T-helper (Th) 17 cells. Recent studies suggested that Foxp3+ Tregs and IL-17+ Th17 cells may be involved in pathogenesis of lichen planus (LP). The objectives of this study were to examine the immunoexpression of Foxp3 and IL-17 in archival paraffin-embedded biopsy specimens from 80 cases of LP (oral LP, n = 42; cutaneous LP, n = 38) and compare against normal control tissues (oral mucosa, n = 10; skin, n = 10). The results showed that the mean number of Foxp3 and IL-17 expression in LP was significantly higher compared to controls, respectively (both P < 0.001). A positive correlation between Foxp3 and IL-17 expression (r = 0.273; P = 0.014) was observed. Moreover, the mean number of Foxp3 expression in oral LP was significantly higher than cutaneous LP (P < 0.001). Collectively, our findings demonstrated the increased expression of Foxp3 and IL-17 in LP lesions including oral and cutaneous variants. Foxp3 expressing in oral LP was higher than cutaneous LP, which may be associated with the difference in clinical behaviour of the two variants of the disease. Further studies are required to investigate the immunopathologic mechanisms and therapeutic target of Foxp3+ Tregs and IL-17+ Th17 cells in LP.
叉头框蛋白3(Foxp3)是调节性T细胞(Tregs)的特异性标志物,而白细胞介素(IL)-17是辅助性T细胞(Th)17细胞的标志性细胞因子。最近的研究表明,Foxp3+调节性T细胞和IL-17+辅助性T细胞17可能参与扁平苔藓(LP)的发病机制。本研究的目的是检测80例扁平苔藓(口腔扁平苔藓,n = 42;皮肤扁平苔藓,n = 38)存档石蜡包埋活检标本中Foxp3和IL-17的免疫表达,并与正常对照组织(口腔黏膜,n = 10;皮肤,n = 10)进行比较。结果显示,与对照组相比,扁平苔藓中Foxp3和IL-17表达的平均数量分别显著更高(均P < 0.001)。观察到Foxp3和IL-17表达之间呈正相关(r = 0.273;P = 0.014)。此外,口腔扁平苔藓中Foxp3表达的平均数量显著高于皮肤扁平苔藓(P < 0.001)。总体而言,我们的研究结果表明,在包括口腔和皮肤变体的扁平苔藓病变中,Foxp3和IL-17表达增加。口腔扁平苔藓中Foxp3的表达高于皮肤扁平苔藓,这可能与该疾病两种变体的临床行为差异有关。需要进一步研究来探讨Foxp3+调节性T细胞和IL-17+辅助性T细胞17在扁平苔藓中的免疫病理机制和治疗靶点。