早期类风湿滑膜组织中T细胞源性细胞因子及激活和增殖标志物的低表达

Tom J.M. Smeets, Radboud J.E.M. Dolhain, André M.M. Miltenburg, Ronella de Kuiper, Ferdinand C. Breedveld, Paul P. Tak
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引用次数: 67

摘要

我们比较了类风湿关节炎(RA)患者在疾病早期和晚期滑膜组织(ST)中T细胞的激活和增殖状态,以了解T细胞驱动的免疫反应是否在疾病过程中发生变化。从12例早期RA患者(<1年)和12例长期RA患者(>5年)。采用免疫组织学方法检测ST中T细胞和干扰素γ (IFN-γ)阳性细胞。为了确定表达白细胞介素-2受体、IFN-γ或增殖相关抗原Ki-67的T细胞的百分比,使用免疫荧光双染色技术。类风湿滑膜中T细胞数量和IFN-γ表达的分数以及表达CD25、IFN-γ或Ki-67的T细胞的百分比不依赖于疾病持续时间。这些结果不支持RA患者ST中T细胞的反应性在疾病早期和晚期不同的假设。数据表明,目前还没有证据表明,t细胞定向干预对滑膜炎症的影响可能在疾病的不同阶段有所不同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Poor Expression of T Cell-Derived Cytokines and Activation and Proliferation Markers in Early Rheumatoid Synovial Tissue

We compared the state of activation and proliferation of T cells in synovial tissue (ST) from rheumatoid arthritis (RA) patients in early and late stages of the disease to find out whether T-cell-driven immune responses vary during the course of the disease. ST was obtained from 12 patients with early RA (< 1 year) and 12 patients with longstanding RA (> 5 years). T cells and interferon-γ (IFN-γ)-positive cells were detected in ST using immunohistologic methods. To determine the percentage of T cells expressing the interleukin-2 receptor, IFN-γ, or the proliferation associated antigen Ki-67, immunofluorescence double-staining techniques were used. The scores for the number of T cells and for the expression of IFN-γ as well as the percentages of T cells expressing CD25, IFN-γ, or Ki-67 in rheumatoid synovium were not dependent on disease duration. These results do not support the assumption that the responsiveness of T cells in ST of RA patients differs between early and late stages of the disease. The data indicate that at present no arguments exist that the effect of T-cell-directed interventions on synovial inflammation might vary in different stages of the disease.

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