结节病患者的细胞因子谱特征

Lazareva Nm, O. Baranova, I. Kudryavtsev, N. A. Arsentieva, N. Liubimova, T. Ses’, M. Ilkovich, A. Totolian
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引用次数: 2

摘要

结节病是一种病因不明的炎症性疾病,对肺部和其他器官造成损害,其特征是形成无坏死的上皮样细胞肉芽肿。以激活不同免疫系统细胞,特别是T淋巴细胞和产生细胞因子为特征的肉芽肿性炎症。我们的研究旨在研究结节病患者血浆中细胞因子谱的特征。我们研究了结节病患者(n=52)的外周血血浆样本。对照血样取自健康志愿者(n=22)。测定46种细胞因子的水平(pg/ml),如下:IL-1α、IL-1β、IL-2、IL-3、IL-4、IL-5、IL-6、IL-7、IL-9、IL-12(p40)、IL-12、p70、IL-13、IL-15、IL-17A、IFNα2、IFNγ、TNFα、TNFβ、IL-11a、IL-10、EGF、FGF-2、Flt3配体、G-CSF、GM-CSF、PDGF-AA、PDGF-AB/BB、TGFα、VEGF-A、sCD40L、CCL2、CCL3、CCL4、CCL5、CCL7。CCL11、CCL17、CCL20、CCL22、CXCL1、CXCL8、CXCL9、CXCL10、CXCL11,CXCL13、CX3CL1。结节病患者的白细胞介素和一些促炎细胞因子水平显著较高,即IL-3,0.70比0.20,p=0.003;IL-4,14.37 vs 3.15,p=0.009;IL-5,1.06 vs 0.89,p<0.001;IL-12(p70),1.27 vs 0.56,p=0.028;IL-17A,1.48 vs 0.43,p<0.001;IFNα2,41.79 vs 25.04,p=0.003;IFNγ,4.13 vs 1.14,p<0.001;TNFα,21.67 vs 6.70,p<0.001;抗炎细胞因子IL-10,1.03 vs 0.45,p=0.019;生长因子:FGF-2,40.08 vs 30.58,p=0.008;G-CSF,24.18 vs 8.21,p=0.006;VEGF-A,42.52 vs 26.76,p=0.048;趋化因子:CCL3,3.86 vs 1.33,p<0001;CCL17,78.24 vs 26.24,p<0.001;CCL20,7.19对5.64,p=0.021;CCL22660.60对405.00,p<0001;CXCL9,4013对1142,p<0001;CXCL10,565.90 vs 196.60,p<0.001;CXCL11230.20对121.10,p=0.018;CX3CL1,56.99 vs 5.16,p<0.001。与健康志愿者组相比,患者的外周血趋化因子CCL11水平显著降低:77.58比124.70,p=0.022。结节病患者细胞因子谱的特征可能表明它们在肉芽肿的形成过程和结果中的重要作用。这些问题需要额外的详细研究,与表型、不同病程和疾病结果进行比较。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Features of cytokine profile in patients with sarcoidosis
Sarcoidosis is an inflammatory disease of unknown etiology with damage to the lungs and other organs characterized by development of necrosis-free epithelioid cell granulomas. Granulomatous inflammation characterized by the activation of different immune systems cells, in particular T lymphocytes, and the cytokines production. Our study was aimed at investigating the characteristics of the cytokine profile of blood plasma in patients with sarcoidosis. We studied peripheral blood plasma samples of patients with sarcoidosis (n = 52). The control blood samples were taken from healthy volunteers (n = 22). The level of 46 cytokines (pg/ml) was determined, as follows: IL-1α, IL-1β, IL-2, IL-3, IL-4, IL-5, IL- 6, IL-7, IL-9, IL-12 (p40), IL-12 (p70), IL-13, IL-15, IL-17A, IFNα2, IFNγ, TNFα, TNFβ, IL- 1ra, IL-10, EGF, FGF-2, Flt3 Ligand, G-CSF, GM-CSF, PDGF-AA, PDGF-AB / BB, TGFα, VEGF-A, sCD40L, CCL2, CCL3, CCL4, CCL5, CCL7, CCL11, CCL17, CCL20, CCL22, CXCL1, CXCL8, CXCL9, CXCL10, CXCL11, CXCL13, CX3CL1. Significantly higher levels of interleukins and some proinflammatory cytokines were found in the patients with sarcoidosis, i.e., IL-3, 0.70 vs 0.20, p = 0.003; IL-4, 14.37 vs 3.15, p = 0.009; IL-5, 1.06 vs 0.89, p < 0.001; IL-12 (p70), 1.27 vs 0.56, p = 0.028; IL-17A, 1.48 vs 0.43, p < 0.001; IFNα2, 41.79 vs 25.04, p = 0.003; IFNγ, 4.13 vs 1.14, p < 0.001; TNFα, 21.67 vs 6.70, p < 0.001; anti-inflammatory cytokine IL-10, 1.03 vs 0.45, p = 0.019; growth factors: FGF-2, 40.08 vs 30.58, p = 0.008, G-CSF, 24.18 vs 8.21, p = 0.006, and VEGF-A, 42.52 vs 26.76, p = 0.048; chemokines: CCL3, 3.86 vs 1.33, p < 0,001; CCL17, 78.24 vs 26.24, p < 0.001; CCL20, 7.19 vs 5.64, p = 0.021; CCL22, 660.60 vs 405.00, p < 0,001; CXCL9, 4013 vs 1142, p < 0,001; CXCL10, 565.90 vs 196.60, p < 0.001; CXCL11, 230.20 vs 121.10, p = 0.018; CX3CL1, 56.99 vs 5.16, p < 0.001. Peripheral blood chemokine CCL11 levels were significantly lower in patients compared to the group of healthy volunteers: 77.58 vs 124.70, p = 0.022. The features of the cytokine profile in patients with sarcoidosis may indicate their important role in the processes of formation and outcomes of granulomas. These issues require an additional detailed study, comparison with phenotypes, differential course and outcomes of the disease.
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