Yu Yongkai, Wang Yidan, Lu Jiawei, Cao Xuechen, Feng Yifei, Pei Tongxin, Lu Yan
Department of Dermatology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Department of Dermatology, The Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou, China.
Inflammation. 2025 Jul 3. doi: 10.1007/s10753-025-02332-2.
Vitiligo and melanoma, while sharing overlapping immune responses and cellular environments, represent distinct dermatological conditions. A comprehensive comparison of the immune microenvironments in vitiligo and melanoma through detailed single-cell analysis has not yet been thoroughly defined.
Integrated single-cell RNA sequencing (scRNA-seq) data were obtained from healthy controls, vitiligo and melanoma patients. Comprehensive analyses including differential gene expression, enrichment analysis, regulatory network, pseudotime trajectory and cell-cell interaction were conducted to elucidate the roles of various cell subtypes and their interactions within the disease microenvironments.
In vitiligo, melanocytes undergo stress-induced activation of multiple cell death pathways and immune activation, whereas in melanoma, they survive by suppressing death signals. The immune microenvironment of vitiligo is dominated by CD8 + T cells, characterized by IFN-γ-CXCL9/10-CXCR3 axis-mediated melanocyte elimination. Stressed fibroblasts and stressed keratinocytes amplify these pro-inflammatory signals. In contrast, the melanoma microenvironment is regulated by Tregs and cancer-associated fibroblasts, leading to impaired cytotoxic function of CD8 + T cells.
The divergent immune microenvironments of vitiligo and melanoma are characterized by immune activation versus immune evasion. These findings provide novel insights into potential therapeutic targets for both conditions.
白癜风和黑色素瘤虽然具有重叠的免疫反应和细胞环境,但代表着不同的皮肤病学病症。尚未通过详细的单细胞分析对白癜风和黑色素瘤的免疫微环境进行全面比较。
从健康对照、白癜风和黑色素瘤患者中获取整合的单细胞RNA测序(scRNA-seq)数据。进行了包括差异基因表达、富集分析、调控网络、伪时间轨迹和细胞间相互作用在内的综合分析,以阐明各种细胞亚型在疾病微环境中的作用及其相互作用。
在白癜风中,黑素细胞经历应激诱导的多种细胞死亡途径激活和免疫激活,而在黑色素瘤中,它们通过抑制死亡信号存活。白癜风的免疫微环境以CD8 + T细胞为主导,其特征在于IFN-γ-CXCL9/10-CXCR3轴介导的黑素细胞清除。应激的成纤维细胞和应激的角质形成细胞放大这些促炎信号。相比之下,黑色素瘤微环境受调节性T细胞和癌症相关成纤维细胞调节,导致CD8 + T细胞的细胞毒性功能受损。
白癜风和黑色素瘤不同的免疫微环境分别以免疫激活和免疫逃避为特征。这些发现为这两种病症的潜在治疗靶点提供了新的见解。