Clinical and molecular markers of vitiligo: a narrative review of early-stage insights into disease activity and treatment response

疾病 白癜风 生物标志物 医学 临床试验 叙述性评论 免疫系统 生物信息学 精密医学 药物开发 免疫疗法 分子生物标志物 表型 免疫失调 生物标志物发现 免疫学 实体瘤疗效评价标准 趋化因子 肿瘤科 临床疾病 个性化医疗 临床表型 疾病严重程度 鉴别诊断 临床研究
作者
Zhe Zhu,Yijian Zhu,Yijie Xuan,Yelin Wu,Yang Liu,Xiuxiu Wang,Li Zhang,Leihong Xiang,Chengfeng Zhang
出处
期刊:British Journal of Dermatology [Oxford University Press]
卷期号:194 (6): 1006-1023
标识
DOI:10.1093/bjd/ljag058
摘要

Vitiligo fluctuates between progressive and quiescent states, complicating decisions about when to intervene, how to select therapy and how to monitor response. In this review, we integrate bedside phenotypes with multilevel molecular readouts to summarize emerging evidence linking clinical signs and biologic signals to disease activity and treatment response in clinical studies. For staging, tool-free and standardized assessments such as Koebner phenomenon, confetti-like depigmentation, Wood's lamp and dermoscopy provide visible clues associated with active disease. Measurements from blood, suction blister fluid and tissue offer complementary insights into local and systemic immune activation, suggesting how molecular signals may relate to progression. For stratification, factors such as age, lesion site, disease stability, comorbidities and dermoscopic border features have been tentatively associated with differential responses to therapies such as phototherapy or transplantation. Similarly, lower baseline levels of inflammatory, chemotactic and cytotoxic markers have been informally aligned with better outcomes in clinical studies. For monitoring, the response phase typically mirrors a reversal of progression: waning inflammatory signalling, reduced effector-cell burden and partial recovery of melanogenic programmes provide molecular parallels to clinical improvement. Across these domains, the interferon-γ-CXCL9/CXCL10-CD8+ T-cell axis emerges as the most recurrent immune signature, demonstrating reproducible associations with activity, prognosis and treatment response. Future work should prioritize harmonized definitions of disease activity, standardized sampling standards and multicentre validation of integrated biomarker panels. It is equally critical to determine whether proposed biomarker thresholds relate to clinically meaningful endpoints, thereby translating early-stage discoveries into reliable frameworks for staging, stratification and monitoring.
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