Komocsi Andras, Lamprecht Peter, Csernok Elena, Mueller Antje, Holl-Ulrich Konstanze, Seitzer Ulrike, Moosig Frank, Schnabel Armin, Gross Wolfgang Ludwig
Department of Rheumatology, University of Luebeck, Luebeck, Germany.
Am J Pathol. 2002 May;160(5):1717-24. doi: 10.1016/s0002-9440(10)61118-2.
To elucidate whether the fraction of CD28(-) T cells within the CD4(+) T-cell population is a major source of Th1-like and proinflammatory cytokine production driving Wegener's granulomatosis (WG) granuloma formation, we analyzed the phenotype and functional characteristics of peripheral blood CD4(+)CD28(-) T cells and of T cells in granulomatous lesions of 12 patients with active WG. Surface markers and intracytoplasmic cytokine and perforin expression were assessed by flow cytometry. Cytokine secretion was measured by enzyme-linked immunosorbent assay. Immunohistological studies demonstrated interferon-gamma and tumor necrosis factor-alpha cytokine positivity attributable to CD4(+)CD28(-) T cells in granulomatous lesions. Peripheral blood CD4(+)CD28(-) T cells expressed CD57, also found on natural killer cells, and intracytoplasmic perforin. They were generally CD25 (interleukin-2 receptor)-negative. CD18 (adhesion molecule beta(2)-integrin) was strongly up-regulated on CD4(+)CD28(-) T cells, whereas only a minority of CD4(+)CD28(+) T cells expressed CD18. CD4(+)CD28(-) T cells appeared as a major source of interferon-gamma and tumor necrosis factor-alpha. In contrast, CD4(+)CD28(+) T cells were able to produce and secrete a wider variety of cytokines including interleukin-2. One-quarter of CD4(+)CD28(+) T cells expressed the activation marker CD25, but they lacked perforin. Thus, CD4(+)CD28(-) T cells appeared more differentiated than CD4(+)CD28(+) T cells. They displayed Th1-like cytokine production and features suggestive of the capability of CD4(+) T-cell-mediated cytotoxicity. CD4(+)CD28(-) T cells may be recruited into granulomatous lesions from the blood via CD18 interaction, and may subsequently promote monocyte accumulation and granuloma formation through their cytokine secretion in WG.
为了阐明CD4(+) T细胞群体中CD28(-) T细胞部分是否是驱动韦格纳肉芽肿(WG)肉芽肿形成的Th1样和促炎细胞因子产生的主要来源,我们分析了12例活动性WG患者外周血CD4(+)CD28(-) T细胞以及肉芽肿病变中T细胞的表型和功能特征。通过流式细胞术评估表面标志物、胞内细胞因子和穿孔素表达。通过酶联免疫吸附测定法测量细胞因子分泌。免疫组织学研究表明,肉芽肿病变中CD4(+)CD28(-) T细胞可产生干扰素-γ和肿瘤坏死因子-α细胞因子。外周血CD4(+)CD28(-) T细胞表达CD57(自然杀伤细胞上也有发现)和胞内穿孔素。它们通常为CD25(白细胞介素-2受体)阴性。CD18(黏附分子β2整合素)在CD4(+)CD28(-) T细胞上强烈上调,而只有少数CD4(+)CD28(+) T细胞表达CD18。CD4(+)CD28(-) T细胞似乎是干扰素-γ和肿瘤坏死因子-α的主要来源。相比之下,CD4(+)CD28(+) T细胞能够产生和分泌更广泛的细胞因子,包括白细胞介素-2。四分之一的CD4(+)CD28(+) T细胞表达活化标志物CD25,但它们缺乏穿孔素。因此,CD4(+)CD28(-) T细胞似乎比CD4(+)CD28(+) T细胞分化程度更高。它们表现出Th1样细胞因子产生以及提示CD4(+) T细胞介导的细胞毒性能力的特征。CD4(+)CD28(-) T细胞可能通过CD18相互作用从血液中募集到肉芽肿病变中,并随后通过其在WG中的细胞因子分泌促进单核细胞积聚和肉芽肿形成。