Mortezagholi Sahar, Babaloo Zohreh, Rahimzadeh Parisa, Ghaedi Mojgan, Namdari Hayedeh, Assar Shirin, Azimi Mohamadabadi Maryam, Salehi Eisa
Department of Immunology, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Iran J Allergy Asthma Immunol. 2016 Jun;15(3):229-36.
Systemic lupus erythematosus (SLE) is a chronic autoimmune disease which results in damage to various organs. Some animal studies have revealed that activation of Toll-like receptors (TLRs) is important in the pathogenesis of SLE. In the present study, the percentage of different immune cell subsets in 35 SLE patients and 38 control subjects was analyzed by flow cytometry. We also assessed the expression of TLR9 in the population of peripheral blood mononuclear cells (PBMCs) including T lymphocytes (CD4+ and CD8+), B lymphocytes (CD19+), NK cells (CD56+) and monocytes (CD14+) in SLE patients and healthy controls. The results showed that the percentage of CD8+ T lymphocytes and CD14+ monocytes were significantly higher (p˂0.001) in the SLE patients than the healthy control subjects. Moreover, the percentage of CD56+ NK cells were significantly lower in the SLE patients than the healthy control subjects (p=0.001). The findings indicated that the expression of TLR9 was significantly higher in CD4+ and CD8+ T lymphocytes and CD19+ B lymphocytes of SLE patients than in control subjects (all p˂0.05). The difference in TLR9 expression are involved in pathogenesis of the SLE, hence it can be used as an indicator for SLE diagnosis.
系统性红斑狼疮(SLE)是一种慢性自身免疫性疾病,可导致多个器官受损。一些动物研究表明,Toll样受体(TLR)的激活在SLE发病机制中起重要作用。在本研究中,通过流式细胞术分析了35例SLE患者和38例对照受试者中不同免疫细胞亚群的百分比。我们还评估了SLE患者和健康对照外周血单个核细胞(PBMC)群体中TLR9的表达,该群体包括T淋巴细胞(CD4 +和CD8 +)、B淋巴细胞(CD19 +)、NK细胞(CD56 +)和单核细胞(CD14 +)。结果显示,SLE患者中CD8 + T淋巴细胞和CD14 +单核细胞的百分比显著高于健康对照受试者(p˂0.001)。此外,SLE患者中CD56 + NK细胞的百分比显著低于健康对照受试者(p = 0.001)。研究结果表明,SLE患者CD4 +和CD8 + T淋巴细胞以及CD19 + B淋巴细胞中TLR9的表达显著高于对照受试者(所有p˂0.05)。TLR9表达的差异参与了SLE的发病机制,因此可作为SLE诊断的指标。