Prpić L, Strbo N, Sotosek V, Gruber F, Podack E R, Rukavina D
Department of Dermatovenerology, Medical Faculty, University of Rijeka, Rijeka, Croatia.
Acta Derm Venereol Suppl (Stockh). 2000(211):14-6. doi: 10.1080/00015550050500059.
There are very few data concerning the role played by cell-mediated cytotoxicity, particularly at the molecular level, in the course of psoriasis. Both cytotoxic T lymphocytes (CTL) and natural killer cells contain in their granules the cytolytic protein perforin, a mediator in cell-mediated cytotoxicity reactions. The aim of this study was to analyze perforin expression in various sets and subsets of perforin-positive peripheral blood lymphocytes in 17 patients with chronic psoriasis vulgaris in the exacerbation phase. The results were compared with those of an age- and sex-matched healthy control group (n = 21). Perforin (intracellular antigen) and cell surface antigens were detected using the simultaneous double-staining method. We found a significant increase in perforin (P) expression in the patient group for CTL (CD3+P+ cells), which are located mostly in the CD8+ population of T lymphocytes (CD8+P+).
关于细胞介导的细胞毒性在银屑病病程中所起的作用,尤其是在分子水平上,相关数据非常少。细胞毒性T淋巴细胞(CTL)和自然杀伤细胞的颗粒中都含有溶细胞蛋白穿孔素,它是细胞介导的细胞毒性反应中的一种介质。本研究的目的是分析17例处于加重期的慢性寻常型银屑病患者中,穿孔素阳性外周血淋巴细胞的不同组和亚组中穿孔素的表达情况。将结果与年龄和性别匹配的健康对照组(n = 21)进行比较。使用同步双重染色法检测穿孔素(细胞内抗原)和细胞表面抗原。我们发现患者组中CTL(CD3 + P +细胞)的穿孔素(P)表达显著增加,CTL主要位于T淋巴细胞的CD8 +群体(CD8 + P +)中。