Devi Mani, Vijayalakshmi Dhanaraj, Dhivya Kumar, Janane Murali
Professor and Head, Department of Oral Pathology, Adhiparasakthi Dental College and Hospital, Chennai, Tamil Nadu, India.
Professor, Department of Oral Pathology, Adhiparasakthi Dental College and Hospital, Chennai, Tamil Nadu, India.
J Clin Diagn Res. 2017 May;11(5):ZC84-ZC86. doi: 10.7860/JCDR/2017/26866.9930. Epub 2017 May 1.
Memory T cells have the ability to survive in a quiescent state for longer periods and are responsible for the rapid responses on subsequent exposure to antigen. Analyzing memory T cells in Oral Lichen planus (OLP) and Lichenoid Mucositis (LM) suggest that these cells may play a role in the immunopathogenic mechanisms.
To identify and evaluate Memory T cells in Lichen Planus (LP), Lichenoid Mucositis (LM) and Normal Mucosa (NM) using CD45RO monoclonal antibody immunohistochemically.
A total of 30 cases (15 cases of OLP and 15 cases of LM) clinically and histopathologically diagnosed, and 10 cases of NM were stained for CD45RO monoclonal antibody, immunohistochemically using Biotin Streptavidin method. Staining intensity of CD45RO expression was statistically analysed using Chi-square Test.
The present study demonstrated a higher expression of CD45RO in connective tissue layer of OLP (53.3% intense staining) when compared to LM (20% intense staining) and no intense staining in NM. The difference in staining intensity pattern between the study groups was statistically significant (p=0.014).
This study demonstrates a statistically significant rise in memory T cells in LP than in LM, indicating the possible different immunopathogenic mechanisms.
记忆性T细胞能够在静止状态下存活较长时间,并负责在后续接触抗原时做出快速反应。对口腔扁平苔藓(OLP)和苔藓样粘膜炎(LM)中的记忆性T细胞进行分析表明,这些细胞可能在免疫致病机制中发挥作用。
使用CD45RO单克隆抗体,通过免疫组织化学方法鉴定和评估扁平苔藓(LP)、苔藓样粘膜炎(LM)和正常黏膜(NM)中的记忆性T细胞。
选取30例临床和组织病理学诊断的病例(15例OLP和15例LM),以及10例NM,采用生物素-链霉亲和素法对CD45RO单克隆抗体进行免疫组织化学染色。使用卡方检验对CD45RO表达的染色强度进行统计学分析。
本研究表明,与LM(20%强染色)相比,OLP结缔组织层中CD45RO的表达更高(53.3%强染色),而NM中无强染色。研究组之间染色强度模式的差异具有统计学意义(p = 0.014)。
本研究表明,LP中记忆性T细胞的数量在统计学上显著高于LM,这表明可能存在不同的免疫致病机制。