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韦格纳肉芽肿病患者表现出 T 调节细胞的相对缺乏和功能障碍。

Patients with Wegener's granulomatosis demonstrate a relative deficiency and functional impairment of T-regulatory cells.

机构信息

Renal Immunobiology, School of Immunity and Infection, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.

出版信息

Immunology. 2010 May;130(1):64-73. doi: 10.1111/j.1365-2567.2009.03213.x. Epub 2010 Jan 27.

Abstract

An increased proportion of CD4(+) CD25(+) T cells has been reported in Wegener's granulomatosis (WG) and may represent an accumulation of regulatory T cells (Treg). CD25 is also expressed on recently activated effector T cells. We have determined the relative proportion of these subsets in a large patient cohort. The fraction of Treg in peripheral blood mononuclear cells from patients and healthy controls was determined by assessment of Foxp3 expression on CD4(+) CD25(+) T cells. The functional activity of Treg was determined by their ability to suppress proliferation and cytokine production in response to proteinase-3. Although WG patients demonstrated an increased fraction of CD4(+) CD25(+) T cells, the percentage of Foxp3-positive cells was decreased. In addition, the percentage of Treg was inversely related to the rate of disease relapse. CD4(+) CD25(hi) T cells were able to suppress T-cell proliferation to proteinase-3 in healthy controls and anti-neutrophil cytoplasm antibody (ANCA)- negative patients (at time of sampling) but not in ANCA-positive patients. In patients with active disease, an increased proportion of CD4(+) Foxp3(+) cells was associated with a more rapid disease remission. Patients with WG demonstrate abnormalities in the number and function of Treg and this is most pronounced in those with most active disease. This information is of value in understanding the pathogenesis and potential treatment of this disease.

摘要

已有报道称,在韦格纳肉芽肿(WG)患者中 CD4(+) CD25(+) T 细胞的比例增加,这可能代表调节性 T 细胞(Treg)的积累。CD25 也表达在最近激活的效应 T 细胞上。我们已经在一个大型患者队列中确定了这些亚群的相对比例。通过评估 CD4(+) CD25(+) T 细胞上 Foxp3 的表达,确定外周血单个核细胞中 Treg 的分数。通过其抑制蛋白酶-3 反应性增殖和细胞因子产生的能力来确定 Treg 的功能活性。尽管 WG 患者表现出 CD4(+) CD25(+) T 细胞比例增加,但 Foxp3 阳性细胞的百分比降低。此外,Treg 的百分比与疾病复发率呈负相关。CD4(+) CD25(hi) T 细胞能够抑制健康对照者和抗中性粒细胞胞质抗体(ANCA)阴性患者(在采样时)对蛋白酶-3 的 T 细胞增殖,但不能抑制 ANCA 阳性患者的 T 细胞增殖。在疾病活动期患者中,CD4(+) Foxp3(+) 细胞比例增加与疾病更快缓解相关。WG 患者的 Treg 数量和功能异常,在疾病最活跃的患者中最为明显。这些信息对于了解疾病的发病机制和潜在治疗方法具有重要价值。

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