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类风湿性关节炎患者滑液和外周血中1型和2型T细胞的分析。

Analysis of type 1 and type 2 T cells in synovial fluid and peripheral blood of patients with rheumatoid arthritis.

作者信息

Kusaba M, Honda J, Fukuda T, Oizumi K

机构信息

First Department of Internal Medicine, Kurume University School of Medicine, Fukuoka, Japan.

出版信息

J Rheumatol. 1998 Aug;25(8):1466-71.

PMID:9712085
Abstract

OBJECTIVE

It has been reported that CD4+ helper T cells play an important role in the pathogenesis of rheumatoid arthritis (RA). We evaluated the presence of intracellular cytokines interleukin 4 (IL-4) and interferon-gamma (IFN-gamma) produced by CD4+ and CD8+ T cells in the synovial fluid and peripheral blood of patients with RA at the single cell level.

METHODS

We used 3 color flow cytometric analysis. Synovial fluid mononuclear cells (SFMC) and peripheral blood mononuclear cells (PBMC) were stimulated with phorbol myristate acetate (PMA) and calcium ionophore. The stimulated SFMC and PBMC were triple stained with conjugated mononuclear antibodies (Mab) against cytokines and surface antigens after fixation and permeabilization with a saponine buffer solution. The cells were analyzed for intracellular cytokines (IFN-gamma, IL-4) and surface antigens (CD3, CD4, CD8) using a flow cytometer.

RESULTS

The CD4/CD8 ratio was significantly lower in SFMC than in PBMC. The positive rates of IFN-gamma producing cells among CD4+ T cells were significantly higher than those of IL-4 producing cells in both the SFMC and the PBMC of patients with active RA. In the SF of these patients, we also found CD8+ T cells that produce IL-4 alone, or both IL-4 and IFN-gamma.

CONCLUSION

In the SF of patients with RA, CD4+ type 1 T cells, which may infiltrate into the synovium and cause pathogenic immune responses in the tissue, are predominant. We believe this cell type also induces migration and activation of CD8+ type 2 T cells into the active site of inflammation, which appears to downregulate the activity of CD4+ type 1 T cells, modulating the excess immune response.

摘要

目的

据报道,CD4+辅助性T细胞在类风湿关节炎(RA)的发病机制中起重要作用。我们在单细胞水平评估了RA患者滑液和外周血中CD4+和CD8+T细胞产生的细胞内细胞因子白细胞介素4(IL-4)和干扰素-γ(IFN-γ)的情况。

方法

我们采用三色流式细胞术分析。用佛波醇肉豆蔻酸酯乙酸酯(PMA)和钙离子载体刺激滑液单核细胞(SFMC)和外周血单核细胞(PBMC)。在用皂角苷缓冲溶液固定和通透处理后,用针对细胞因子和表面抗原的结合单克隆抗体(Mab)对刺激后的SFMC和PBMC进行三重染色。使用流式细胞仪分析细胞内细胞因子(IFN-γ、IL-4)和表面抗原(CD3、CD4、CD8)。

结果

SFMC中的CD4/CD8比值显著低于PBMC。在活动期RA患者的SFMC和PBMC中,CD4+T细胞中产生IFN-γ的细胞阳性率显著高于产生IL-4的细胞阳性率。在这些患者的滑液中,我们还发现了单独产生IL-4或同时产生IL-4和IFN-γ的CD8+T细胞。

结论

在RA患者的滑液中,可能浸润到滑膜并在组织中引起致病性免疫反应的CD4+1型T细胞占主导。我们认为这种细胞类型还诱导CD8+2型T细胞迁移并激活到炎症活动部位,这似乎下调了CD4+1型T细胞的活性,调节过度的免疫反应。

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