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Influence of low dose irradiation on differentiation, maturation and T-cell activation of human dendritic cells

机译:低剂量照射对人树突状细胞分化,成熟和T细胞活化的影响

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Ionizing irradiation could act directly on immune cells and may induce bystander effects mediated by soluble factors that are released by the irradiated cells. This is the first study analyzing both the direct effect of low dose ionizing radiation (LDIR) on the maturation and cytokine release of human dendritic cells (DCs) and the functional consequences for co-cultured T-cells. We showed that irradiation of DC-precursors in vitro does not influence surface marker expression or cytokine profile of immature DCs nor of mature DCs after LPS treatment. There was no difference of single dose irradiation versus fractionated irradiation protocols on the behavior of the mature DCs. Further, the low dose irradiation did not change the capacity of the DCs to stimulate T-cell proliferation. But the irradiation of the co-culture of DCs and T-cells revealed significantly lower proliferation of T-cells with higher doses. Summarizing the data from approx. 50 DC preparations there is no significant effect of low dose ionizing irradiation on the cytokine profile, surface marker expression and maturation of DCs in vitro although functional consequences cannot be excluded.
机译:电离辐射可直接作用于免疫细胞,并可诱导受辐射细胞释放的可溶性因子介导的旁观者效应。这是首次研究低剂量电离辐射(LDIR)对人树突状细胞(DC)成熟和细胞因子释放的直接影响以及共培养T细胞的功能后果。我们显示,在LPS处理后,体外DC前体的辐射不会影响未成熟DC或成熟DC的表面标志物表达或细胞因子谱。在成熟DC的行为方面,单剂量辐照与分次辐照方案没有差异。此外,低剂量照射并未改变DC刺激T细胞增殖的能力。但是,DC和T细胞共培养物的照射显示,高剂量T细胞的增殖明显降低。汇总约的数据。 50种DC制剂,尽管不能排除功能性后果,但低剂量电离辐射对DC的细胞因子谱,表面标志物表达和DC成熟没有明显影响。

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