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复发性阿弗他溃疡患者外周血中1型细胞因子占优势且CD4(+)CD25(+高表达)调节性T细胞数量减少。

Predominance of Type 1 cytokines and decreased number of CD4(+)CD25(+high) T regulatory cells in peripheral blood of patients with recurrent aphthous ulcerations.

作者信息

Lewkowicz Natalia, Lewkowicz Przemysław, Banasik Małgorzata, Kurnatowska Anna, Tchórzewski Henryk

机构信息

Department of Periodontal and Oral Mucosal Diseases, Medical University of Lodz, Pomorska Street 251, 92-213 Lodz, Poland.

出版信息

Immunol Lett. 2005 Jun 15;99(1):57-62. doi: 10.1016/j.imlet.2005.01.002. Epub 2005 Jan 22.

Abstract

Recurrent aphthous ulcerations (RAU) are a chronic inflammatory disease with evidence of inappropriate immune response. Previous studies have suggested cell-mediated activation of immune response towards common micro-organisms of oral cavity in RAU. In this investigation, we explored cytokine production by peripheral blood mononuclear cells (PBMC) and T regulatory cell population in blood of active and remission RAU patients as crucial factors for maintenance of peripheral tolerance. Ten patients with minor RAU and 12 healthy individuals were selected for the study. Cytokine levels were analysed in supernatants using Cytometric Bead Array Kit for flow cytometry and ELISA. We have demonstrated increased production of Type 1 cytokines IL-2, IFN-gamma and TNF-alpha as well as IL-5, IL-6 and IL-8 by peripheral blood mononuclear cells in RAU. In contrast, IL-10 and TGF-beta anti-inflammatory cytokine production was decreased in RAU patients compared to healthy individuals. Moreover, we have found that CD4(+)CD25(+high) T regulatory cell proportion was decreased in RAU and represented 3.58+/-0.654% of CD4(+) T cells in active RAU, 4.66+/-0.561% of CD4(+) T cells in remission RAU, whereas in healthy controls CD4(+)CD25(+high) T cells represented 7.30+/-1.238% of CD4(+) T cells (p<0.001). Thus, the obtained results indicate that disproportion in cytokine production may be contributing factor in the pathogenesis of RAU. Alteration in the number of CD4(+)CD25(+high) T regulatory cells in RAU may additionally influence the development of the disease. We propose that imbalance in pro- and anti-inflammatory cytokine network may lead to the breakdown of peripheral tolerance in RAU and the excessive immune response towards harmless micro-organisms colonized oral mucosa or self-antigens.

摘要

复发性阿弗他溃疡(RAU)是一种慢性炎症性疾病,有证据表明存在不适当的免疫反应。先前的研究表明,RAU中针对口腔常见微生物的免疫反应存在细胞介导的激活。在本研究中,我们探讨了活动期和缓解期RAU患者外周血单个核细胞(PBMC)产生的细胞因子以及血液中T调节细胞群体,将其作为维持外周耐受的关键因素。选择10例轻度RAU患者和12名健康个体进行研究。使用流式细胞术细胞计数微珠阵列试剂盒和酶联免疫吸附测定法分析上清液中的细胞因子水平。我们已证明,RAU患者外周血单个核细胞产生的1型细胞因子白细胞介素-2(IL-2)、γ干扰素(IFN-γ)和肿瘤坏死因子-α(TNF-α)以及IL-5、IL-6和IL-8增加。相比之下,与健康个体相比,RAU患者中抗炎细胞因子IL-10和转化生长因子-β(TGF-β)的产生减少。此外,我们发现RAU患者中CD4(+)CD25(+高) T调节细胞比例降低,在活动期RAU中占CD4(+) T细胞的3.58±0.654%,在缓解期RAU中占CD4(+) T细胞的4.66±0.561%,而在健康对照中,CD4(+)CD25(+高) T细胞占CD4(+) T细胞的7.30±1.238%(p<0.001)。因此,获得的结果表明,细胞因子产生的失衡可能是RAU发病机制中的一个促成因素。RAU中CD4(+)CD25(+高) T调节细胞数量的改变可能会额外影响疾病的发展。我们提出,促炎和抗炎细胞因子网络的失衡可能导致RAU中外周耐受的破坏以及对定植于口腔黏膜的无害微生物或自身抗原的过度免疫反应。

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