Speeckaert Reinhart, Voet Sofie, Hoste Esther, van Geel Nanja
Department of Dermatology, Ghent University Hospital, Ghent, Belgium.
Inflammation Research Center, VIB, Ghent, Belgium; Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
J Invest Dermatol. 2017 Jul;137(7):1445-1453. doi: 10.1016/j.jid.2017.01.033. Epub 2017 Feb 14.
Vitiligo is a chronic skin condition characterized by progressive depigmentation of the skin. S100B is a damage-associated molecular pattern protein expressed in melanocytes that has been proposed as a marker of melanocyte cytotoxicity. Although the use of S100B as a biomarker in melanoma is well established, to our knowledge its association with vitiligo activity has not yet been investigated. Here, we show that S100B serum levels were significantly increased in patients with active nonsegmental vitiligo and strongly correlated with the affected body surface area. Prospective follow-up showed a predictive value of serum S100B levels on disease progression. In vitro experiments using repeated freeze-thaw procedures showed an intracellular up-regulation of S100B in normal and vitiligo melanocytes before an extensive release in the environment. This phenomenon may explain the increased S100B serum values in the active phase of vitiligo. In a monobenzone-induced vitiligo mouse model we could show the potential of S100B inhibition as a therapeutic strategy in vitiligo. In conclusion, this report shows the possible use of S100B as a biomarker for disease activity in vitiligo. Our data suggest that this damage-associated molecular pattern protein could play a substantial role in the pathogenesis of vitiligo and may be a potential new target for treatment.
白癜风是一种慢性皮肤病,其特征是皮肤进行性色素脱失。S100B是一种在黑素细胞中表达的损伤相关分子模式蛋白,已被提议作为黑素细胞细胞毒性的标志物。尽管S100B作为黑色素瘤生物标志物的应用已得到充分证实,但据我们所知,其与白癜风活动的关联尚未得到研究。在此,我们表明,活动性非节段性白癜风患者的S100B血清水平显著升高,且与受累体表面积密切相关。前瞻性随访显示血清S100B水平对疾病进展具有预测价值。使用反复冻融程序的体外实验表明,在正常和白癜风黑素细胞中,S100B在大量释放到环境之前会在细胞内上调。这种现象可能解释了白癜风活动期S100B血清值升高的原因。在单苯甲醚诱导的白癜风小鼠模型中,我们可以证明抑制S100B作为白癜风治疗策略的潜力。总之,本报告表明S100B可能作为白癜风疾病活动的生物标志物。我们的数据表明,这种损伤相关分子模式蛋白可能在白癜风的发病机制中起重要作用,并且可能是一个潜在的新治疗靶点。