首页> 外文期刊>Respiration: International Review of Thoracic Diseases >Direct demonstration of the productive capability of cytokines at the single cell level in lung sarcoidosis using multicolor cytometry.
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Direct demonstration of the productive capability of cytokines at the single cell level in lung sarcoidosis using multicolor cytometry.

机译:使用多色细胞术直接证明了肺结节病在单细胞水平上细胞因子的生产能力。

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BACKGROUND: Sarcoidosis is a chronic systemic disorder of unknown etiology characterized by noncaseating epithelioid cell granulomatous lesions, around which an increasing number of CD4+ T cells infiltrate. These CD4+ T cells may release interferon-gamma (IFN-gamma) and interleukin-2 (IL-2). These cytokines are considered to play an important role in pathogenesis of sarcoidosis. METHODS: We employed a modification of Jung's method using multicolor flow cytometry to assess the capability of single cells obtained from bronchoalveolar lavage (BAL) fluid to produce various cytokines. BAL CD4+ T cell production of IFN-gamma, IL-2 and IL-4 after phorbol ester and ionomycin stimulation were studied. RESULTS: The percentage of IFN-gamma- and IL-2-producing CD4+ T cells was significantly higher in patients with sarcoidosis compared to healthy volunteers [84.7 +/- 7.5 vs. 51.2 +/- 14.8% (p < 0.005), and 75.3 +/- 8.7 vs. 39.8 +/-11.0% (p < 0.001), respectively]. No significant difference in the percentage of IL-4-producing CD4+ T cells was noted (1.2 +/- 0.6 vs. 3.5 +/- 2.6%; not significant), whereas the absolute number of IL-4-producing CD4+ T cells was significantly higher in patients with sarcoidosis compared to healthy volunteers (563.6 +/- 330.2 vs. 50.9 +/- 66.9/ml; p < 0.005). In the IL-4-producing CD4+ T cells, about 80% of cells concomitantly produced IFN-gamma and more than 60% of cells also produced IL-2. CONCLUSION: We demonstrate that Th1-like-producing cells are predominant in the CD4+ as well as in the CD8+ T cell subset of patients with sarcoidosis. We for the first time demonstrated concomitant capabilities of BAL CD4+ T cells to produce Th1 and Th2 cytokines at the single cell level by multicolor flow cytometry.
机译:背景:结节病是一种病因不明的慢性全身性疾病,其特征是非干酪样上皮样细胞肉芽肿性病变,周围有越来越多的CD4 + T细胞浸润。这些CD4 + T细胞可能释放干扰素-γ(IFN-γ)和白介素2(IL-2)。这些细胞因子被认为在结节病的发病机理中起重要作用。方法:我们采用改良的Jung方法,使用多色流式细胞术评估从支气管肺泡灌洗(BAL)液获得的单细胞产生各种细胞因子的能力。研究了佛波酯和离子霉素刺激后BAL CD4 + T细胞产生的IFN-γ,IL-2和IL-4。结果:结节病患者中产生IFN-γ和IL-2的CD4 + T细胞百分比显着高于健康志愿者[84.7 +/- 7.5与51.2 +/- 14.8%(p <0.005),和75.3 +/- 8.7与39.8 +/- 11.0%(p <0.001)]。没有观察到产生IL-4的CD4 + T细胞百分比的显着差异(1.2 +/- 0.6对3.5 +/- 2.6%;不显着),而产生IL-4的CD4 + T细胞的绝对数量与健康志愿者相比,结节病患者的病死率显着更高(563.6 +/- 330.2 / v。50.9 +/- 66.9 / ml; p <0.005)。在产生IL-4的CD4 + T细胞中,约80%的细胞同时产生IFN-γ,超过60%的细胞也产生IL-2。结论:我们证明结节病患者的CD4 +以及CD8 + T细胞亚群中均产生Th1样细胞。我们首次通过多色流式细胞术证明了BAL CD4 + T细胞在单细胞水平上产生Th1和Th2细胞因子的伴随能力。

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