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Suppressive effect of TNF-α and IL-1 on alveolar fibroblast proliferation in sarcoidosis

机译:TNF-α和IL-1对结节病肺泡成纤维细胞增殖的抑制作用

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摘要

The nature of soluble factors that regulate fibroblast proliferation have not been finally characterized. Our aim was to study the role of tumour necrosis factor α (TNF-α) and interleukin-1 (IL-1) in the suppressive activity of alveolar macrophages on autologous lung fibroblasts proliferation in sarcoidosis. We found that supernatants recovered from alveolar macrophages suppressed the proliferation of alveolar fibroblast in sarcoidosis by 35.5 ± 1.13% compared to 3 ± 16% in controls (p < 0.001 between the two groups). This suppression correlated with high content of TNF-α and IL-1 in sarcoidosis patients stage II-III (7.7 ± 2.9 ng/ml TNF-α and 157 ± 53 U/ml IL-1 compared to 3.4 ± 2.4 ng/ml TNF-α and 43 U/ml IL-1 in controls; p < 0.01 and p < 0.001, respectively). Both cytokines in sarcoidosis stage I were within the normal ranges. Exogenous TNF-α (1000-0.5 ng/ml) and IL-1 (500-0.24 ng/ml) had an additive suppressive activity on fibroblast proliferation which was partially reversed by indomethacin.
机译:调节成纤维细胞增殖的可溶性因子的性质尚未最终确定。我们的目的是研究肿瘤坏死因子α(TNF-α)和白介素-1(IL-1)在肺泡巨噬细胞对结节病中自体肺成纤维细胞增殖的抑制作用中的作用。我们发现,从肺泡巨噬细胞中回收的上清液可将结节病中的肺泡成纤维细胞增殖抑制35.5±1.13%,而对照组为3±16%(两组之间p <0.001)。这种抑制与结节病患者II-III期的高TNF-α和IL-1含量相关(7.7±2.9 ng / mlTNF-α和157±53 U / ml IL-1,而3.4±2.4 ng / ml TNF对照中的-α和43 U / ml IL-1;分别为p <0.01和p <0.001)。结节病I期的两种细胞因子均在正常范围内。外源性TNF-α(1000-0.5 ng / ml)和IL-1(500-0.24 ng / ml)对成纤维细胞增殖具有累加抑制活性,吲哚美辛可部分逆转该抑制活性。

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