Department of Dermatology, University Hospital Zurich, 8091 Zurich, Switzerland.
Empa, Swiss Federal Laboratories for Materials Science and Technology, Laboratory for Biomimetic Membranes and Textiles, Laboratory for Biointerfaces, 9014 St. Gallen, Switzerland.
Int J Mol Sci. 2024 Sep 8;25(17):9720. doi: 10.3390/ijms25179720.
Lichen planus (LP) is a highly prevalent inflammatory skin disease. While various clinical subtypes have been defined, detailed comparisons of these variants are lacking. This study aimed to elucidate differences in gene expression and cellular composition across LP subtypes. Lesional skin biopsies from 28 LP patients (classical, oral, genital, and lichen planopilaris) and seven non-diseased skin controls (NDC) were analyzed. Gene expression profiling of 730 inflammation-related genes was conducted using NanoString. Immune cell compositions were assessed by multiplex immunohistochemistry. Gene expression profiles revealed unique inflammatory signatures for each LP subtype. Lichen planopilaris exhibited the most divergence, with downregulated gene expression and upregulation of complement pathway genes (), along with elevated M2 macrophages. Oral and genital LP demonstrated similar profiles with strong upregulation of TNF-related and Toll-like receptor-associated genes. Oral LP showed the highest upregulation of cytotoxicity-associated genes, as well as high numbers of CD8+ IL-17A+ (Tc17) cells (8.02%). Interferon gene signatures were strongly upregulated in oral and classical LP. The study highlights distinct differences in inflammatory gene expression and cell composition across LP subtypes, emphasizing the need for tailored therapeutic approaches.
扁平苔藓(LP)是一种高度流行的炎症性皮肤病。虽然已经定义了各种临床亚型,但这些变体之间的详细比较仍缺乏。本研究旨在阐明 LP 亚型之间在基因表达和细胞组成上的差异。对 28 名 LP 患者(经典型、口腔型、生殖器型和扁平苔藓型)和 7 名非病变皮肤对照(NDC)的皮损皮肤活检进行了分析。使用 NanoString 对 730 个与炎症相关的基因进行了基因表达谱分析。通过多重免疫组化评估免疫细胞组成。基因表达谱显示每个 LP 亚型都具有独特的炎症特征。扁平苔藓型表现出最大的差异,表现为下调的基因表达和补体途径基因的上调(),同时 M2 巨噬细胞增加。口腔型和生殖器型 LP 表现出相似的特征,强烈上调 TNF 相关和 Toll 样受体相关基因。口腔型 LP 表现出最高的细胞毒性相关基因上调,以及大量的 CD8+IL-17A+(Tc17)细胞(8.02%)。干扰素基因特征在口腔型和经典型 LP 中强烈上调。该研究强调了 LP 亚型之间在炎症基因表达和细胞组成上的明显差异,强调了需要针对特定治疗方法的必要性。