Immunological markers changes in pediatric immune Thrombocytopenic Purpura

S. Hamada, Ola Al Diwany, Radwa S. Shahin
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Abstract

Background Individuals with immune thrombocytopenic purpura (ITP) have cellular immune responses that show the characteristics of tolerance mechanisms that have broken down. Objectives This study aimed to assess the percentage of regulatory T cells (Tregs) and CD4 lymphocytes that express CXCR6 in untreated newly diagnosed ITP in pediatric patients and their correlation with each other, the platelet (PLT) count and other PLT indices. Patients and methods A case–control study was carried out that included 40 pediatric patients with ITP, and 20 age-matched and sex-matched healthy controls were selected from Benha Children Hospital hematology clinic. Assessment of CD4+, CD25+, and FoxP3+as markers of Treg cells and also expression of the CXCR6 receptor on CD4+ T lymphocytes to evaluate the percentage of Tregs and CD4/CXCR6 +T lymphocytes were investigated by flow cytometry. Results There was a marked reduction in CD4/CXCR6 and Tregs (P=0.02 and 0.001) in the ITP group versus the control group. In contrast, there was a marked increase in CD4/CD25+cells (P=0.002) in the ITP group compared with the control group. There was a considerable reduction in the PLT count and the hemoglobin concentration in the ITP group compared with the control group (P=0.000 and 0.01), while there was a significant increase in large platelet cell ratio and platelet distribution width in the ITP group in comparison to the control group (P=0.04 for both of them); also, there were insignificant differences in total leukocytic count and mean platelet volume in the ITP group in comparison to the control group (P=0.28 and 0.77). Conclusion There was a significant decrease in the concentration of CD4+ cells that express CXCR6+ and Treg percentage in ITP patients as compared with the controls, which may explain the defect in immune self-tolerance in ITP patients.
儿童免疫性血小板减少性紫癜的免疫学指标变化
背景:患有免疫性血小板减少性紫癜(ITP)的个体具有细胞免疫反应,显示耐受机制已经崩溃的特征。本研究旨在评估未经治疗的儿科新诊断ITP患者中表达CXCR6的调节性T细胞(Tregs)和CD4淋巴细胞的百分比及其与血小板(PLT)计数和其他PLT指标的相关性。患者与方法采用病例对照研究,选取本哈儿童医院血液科门诊40例ITP患儿和20例年龄匹配、性别匹配的健康对照。采用流式细胞术检测CD4+、CD25+、FoxP3+作为Treg细胞的标志物,以及CXCR6受体在CD4+ T淋巴细胞上的表达,评估Treg和CD4/CXCR6 +T淋巴细胞的百分比。结果与对照组相比,ITP组CD4/CXCR6和Tregs明显降低(P=0.02和0.001)。与对照组相比,ITP组CD4/CD25+细胞明显增加(P=0.002)。ITP组血小板计数和血红蛋白浓度较对照组显著降低(P=0.000和0.01),大血小板细胞比例和血小板分布宽度较对照组显著增加(P=0.04);ITP组总白细胞计数和平均血小板体积与对照组比较差异无统计学意义(P=0.28和0.77)。结论与对照组相比,ITP患者表达CXCR6+的CD4+细胞浓度和Treg百分比明显降低,这可能解释了ITP患者免疫自身耐受缺陷的原因。
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