Ramezani Mazaher, Hashemi Bita-Sadat, Khazaei Sedigheh, Rezaei Mansour, Ebrahimi Ali, Sadeghi Masoud
Molecular Pathology Research Center, Imam Reza University Hospital, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Department of Biostatistics and Epidemiology, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Indian J Pathol Microbiol. 2017 Apr-Jun;60(2):172-176. doi: 10.4103/0377-4929.208381.
Cluster of differentiation (CD) markers is a classification system for monoclonal antibodies against cell surface molecules on leukocytes and antigens from other cells.
The aim of this study is to evaluate immunohistochemical markers in patients with discoid lupus erythematosus (DLE) and lichen planus (LP) and correlation of these markers in two groups and with the normal group in the West of Iran.
Analytical cross-sectional study.
This study was performed on paraffin blocks of DLE and LP patients with normal group (21, 21 and 16 cases, respectively) between 2009 and 2012. Formalin-fixed, paraffin-embedded tissue sections from each DLE, LP, and normal skin biopsy specimen were cut into 4-μ thick sections and mounted on glass slides. Initial sections were stained with hematoxylin and eosin. Primary antihuman antibodies against CD3, CD20, CD34, and Bcl-2 were applied. Positive control samples for CD3, CD20, and Bcl-2 were received from lymph nodes and for CD34 from dermal microvessels.
SPSS version 19 (SPSS, Inc., Chicago, USA) and Microsoft Excel 2007.
The mean staining for four markers was more significant in DLE and LP groups compared to normal group and for CD34 and CD3 was more significant in LP groups versus DLE group.
CD3+, CD34+, Bcl-2+, and CD20+ cells are significantly higher in DLE and LP lesional skins versus normal skin. In addition, there were higher expressions of CD3 and CD34 in LP lesional skin versus DLE lesional skin.
分化簇(CD)标志物是一种针对白细胞表面分子和其他细胞抗原的单克隆抗体分类系统。
本研究旨在评估盘状红斑狼疮(DLE)和扁平苔藓(LP)患者的免疫组织化学标志物,以及这两组标志物与伊朗西部正常组之间的相关性。
分析性横断面研究。
本研究在2009年至2012年期间对DLE和LP患者以及正常组(分别为21例、21例和16例)的石蜡块进行。将来自每个DLE、LP和正常皮肤活检标本的福尔马林固定、石蜡包埋组织切片切成4微米厚的切片,并安装在载玻片上。初始切片用苏木精和伊红染色。应用针对CD3、CD20、CD34和Bcl-2的抗人一抗。CD3、CD20和Bcl-2的阳性对照样本取自淋巴结,CD34的阳性对照样本取自真皮微血管。
SPSS 19版(SPSS公司,美国芝加哥)和Microsoft Excel 2007。
与正常组相比,DLE和LP组中四种标志物的平均染色更显著,并且与DLE组相比,LP组中CD34和CD3的染色更显著。
与正常皮肤相比,DLE和LP病变皮肤中的CD3+、CD34+、Bcl-2+和CD20+细胞显著更高。此外,与DLE病变皮肤相比,LP病变皮肤中CD3和CD34的表达更高。