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Altered expression of T cell Immunoglobulin-Mucin (Tim) molecules in peripheral blood mononuclear cells in aplastic anemia

机译:再生障碍性贫血中外周血单核细胞中T细胞免疫球蛋白-粘蛋白(Tim)分子的表达改变

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摘要

To evaluate the balance between T-cell immunoglobulin and mucin domain (Tim) molecules(Tim)-1 and Tim-3 in patients with aplastic anemia (AA), plasma IFN-γ and IL-4 levels were measured in patients with active AA (n = 41), AA in remission (n = 29) and in healthy subjects (n = 40) by enzyme linked immunosorbent assay (ELISA). Using real-time quantitative polymerase chain reaction (RT-PCR), the mRNA expression of IFN-γ, IL-4, Tim-1 and Tim-3 were studied in all subjects. The results showed that the expression of Tim-3 in newly diagnosed patients was significantly deceased, compared with the controls. Meanwhile, Tim-1 mRNA expression in the active AA group was not significantly reduced, which resulted in a declined ratio of Tim-3/Tim-1 in patients with active disease. During the remission stages, the levels of these transcription factors were comparable with those observed in the healthy controls. These findings are the first data on the expression of the Tim-1 and Tim-3 molecules in AA. The reduced levels of Tim-3/Tim-1 in PBMCs during the active stages of disease suggest that they may play a possible role in the pathogenesis and course of AA.
机译:为了评估再生障碍性贫血(AA)患者的T细胞免疫球蛋白与粘蛋白结构域(Tim)-1和Tim-3之间的平衡,测定了活动性AA患者的血浆IFN-γ和IL-4水平(n = 41),通过酶联免疫吸附试验(ELISA)缓解的AA(n = 29)和健康受试者(n = 40)。使用实时定量聚合酶链反应(RT-PCR),在所有受试者中研究了IFN-γ,IL-4,Tim-1和Tim-3的mRNA表达。结果表明,与对照组相比,新诊断患者中Tim-3的表达明显降低。同时,活动性AA组中Tim-1 mRNA的表达没有明显降低,导致活动性疾病患者中Tim-3 / Tim-1的比例下降。在缓解阶段,这些转录因子的水平与健康对照组中观察到的水平相当。这些发现是有关AA中Tim-1和Tim-3分子表达的第一个数据。在疾病活跃期,PBMC中Tim-3 / Tim-1的水平降低表明它们可能在AA的发病机理和病程中发挥可能的作用。

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