C. G. Bhakta Institute of Biotechnology, Faculty of Science, Uka Tarsadia University, Bardoli, Surat, 394 350 Gujarat, India.
J Immunol Res. 2022 Sep 16;2022:6952299. doi: 10.1155/2022/6952299. eCollection 2022.
Vitiligo is a noncontagious autoimmune skin depigmenting disease. Regulatory T cells (Tregs) play a key role in maintaining peripheral tolerance; however, Tregs' number, suppressive function, and associated suppressive molecules (FOXP3, IL-10, and TGF-) are found to be reduced in vitiligo patients. Although, the role of Tregs in vitiligo pathogenesis is well established, there are several contrary findings which suggest a controversial role of Tregs in vitiligo. Therefore, to clarify the role of Tregs in vitiligo pathogenesis, we aimed to study Tregs' frequency, suppressive capacity, and associated suppressive molecules (FOXP3, IL-10, and TGF-) in vitiligo patients through meta-analysis approach. A total of 30 studies involving 1223 vitiligo patients and 1109 controls were included in the study. Pooled results from our meta-analysis suggested significantly reduced Treg cells' frequency in vitiligo patients ( = 0.002). Interestingly, Tregs' suppressive capacity was also significantly reduced in vitiligo patients ( = 0.0002); specifically, Treg-mediated suppression of CD8T cells was impaired in vitiligo patients ( < 0.00001). Moreover, FOXP3, a key Tregs' transcription factor, was significantly reduced in blood and skin of vitiligo patients ( < 0.00001). Intriguingly, the FOXP3 expression was significantly reduced in the lesional skin as compared to perilesional and nonlesional skin ( = 0.007 and = 0.04). Furthermore, the expression of key Treg-associated suppressive cytokines IL-10 and TGF- were significantly reduced in vitiligo patients ( = 0.0005 and = 0.01). The disease activity-based analysis suggested for reduced Tregs' frequency and FOXP3 expression in active vitiligo patients ( = 0.05 and = 0.01). We also studied the effect of microRNA-based treatment, narrow band-UVB phototherapy, and Treg-associated treatments on Tregs' frequency, FOXP3, and IL-10 expression. Interestingly, we found increased Tregs' frequency, FOXP3, and IL-10 expression after the treatment ( = 0.007, < 0.0001, and = 0.002). Overall, our meta-analysis suggests that the Tregs play a crucial role in pathogenesis and progression of vitiligo, and hence, Treg-based therapeutic interventions could be effective in vitiligo patients.
白癜风是一种非传染性自身免疫性皮肤色素脱失疾病。调节性 T 细胞(Tregs)在维持外周耐受方面发挥着关键作用;然而,白癜风患者的 Tregs 数量、抑制功能以及相关的抑制分子(FOXP3、IL-10 和 TGF-)都发现减少了。尽管 Tregs 在白癜风发病机制中的作用已得到充分证实,但也有一些相反的发现表明 Tregs 在白癜风中发挥着有争议的作用。因此,为了阐明 Tregs 在白癜风发病机制中的作用,我们旨在通过荟萃分析的方法研究白癜风患者 Tregs 的频率、抑制能力以及相关的抑制分子(FOXP3、IL-10 和 TGF-)。这项研究共纳入了 30 项研究,涉及 1223 名白癜风患者和 1109 名对照者。荟萃分析的汇总结果表明,白癜风患者 Treg 细胞的频率显著降低( = 0.002)。有趣的是,白癜风患者的 Tregs 抑制能力也显著降低( = 0.0002);具体来说,Treg 介导的 CD8T 细胞抑制在白癜风患者中受损( < 0.00001)。此外,FOXP3,一种关键的 Tregs 转录因子,在白癜风患者的血液和皮肤中显著减少( < 0.00001)。有趣的是,与非皮损和皮损旁皮肤相比,皮损中的 FOXP3 表达显著降低( = 0.007 和 = 0.04)。此外,白癜风患者中关键的 Treg 相关抑制性细胞因子 IL-10 和 TGF-的表达也显著降低( = 0.0005 和 = 0.01)。基于疾病活动的分析表明,活跃的白癜风患者的 Tregs 频率和 FOXP3 表达降低( = 0.05 和 = 0.01)。我们还研究了基于 microRNA 的治疗、窄带 UVB 光疗和 Treg 相关治疗对 Tregs 频率、FOXP3 和 IL-10 表达的影响。有趣的是,我们发现治疗后 Tregs 频率、FOXP3 和 IL-10 表达增加( = 0.007、 < 0.0001 和 = 0.002)。总体而言,我们的荟萃分析表明 Tregs 在白癜风的发病和进展中起着关键作用,因此,Treg 为基础的治疗干预可能对白癜风患者有效。