Department of Dermatology, Venereology and Paediatric Dermatology, Medical University of Lublin, Lublin, Poland.
Experimental Hematooncology Department, Medical University of Lublin, Lublin, Poland.
Mediators Inflamm. 2017;2017:5385102. doi: 10.1155/2017/5385102. Epub 2017 Oct 17.
Psoriasis is a chronic inflammatory disease mediated by T cell immunity. Programmed death 1 (PD-1), a coinhibitory receptor, plays an important role in immune regulation and maintaining peripheral tolerance. The aim of the study was to compare the expression of PD-1 on the peripheral T cells between psoriatic patients and healthy controls. The study included 75 psoriatic patients and 52 healthy volunteers. The percentages and absolute numbers of CD3, CD4, CD8, CD4PD-1, and CD8PD-1 T cells were analyzed using flow cytometry. The absolute numbers and percentages of CD4PD-1 and CD8PD-1 T cells were significantly decreased in the psoriatic patients in comparison with the control group. No significant correlations were found between the absolute numbers and percentages of CD4PD-1 or CD8PD-1 T cells and clinical characteristics of psoriasis. Decreased PD-1 expression on the T cells may be responsible for impaired negative regulation of immune response in psoriasis pathogenesis.
银屑病是一种由 T 细胞免疫介导的慢性炎症性疾病。程序性死亡受体 1(PD-1)是一种共抑制受体,在免疫调节和维持外周耐受中发挥重要作用。本研究旨在比较银屑病患者和健康对照者外周 T 细胞 PD-1 的表达。该研究纳入了 75 例银屑病患者和 52 例健康志愿者。采用流式细胞术分析 CD3、CD4、CD8、CD4PD-1 和 CD8PD-1 T 细胞的百分比和绝对数。与对照组相比,银屑病患者的 CD4PD-1 和 CD8PD-1 T 细胞的绝对数和百分比显著降低。CD4PD-1 或 CD8PD-1 T 细胞的绝对数和百分比与银屑病的临床特征之间无显著相关性。T 细胞上 PD-1 表达的降低可能是导致银屑病发病机制中免疫反应负调控受损的原因。