首页> 外文期刊>Transfusion and apheresis science: official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis >IFN-gamma and TNF-alpha production in gamma-irradiated blood units by mononuclear cells and GVHD prevention.
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IFN-gamma and TNF-alpha production in gamma-irradiated blood units by mononuclear cells and GVHD prevention.

机译:单核细胞和GVHD预防在γ辐射的血液单位中产生IFN-γ和TNF-α。

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摘要

Gamma-radiation of blood products is considered the mainstay of transfusion-associated graft-versus-host disease prevention. Previous studies have detected lymphocyte inhibition rate in blood components just one time after irradiation but there is evidence of cellular variability with production of cytokines at different storage time which could be related with irradiation activity and cellular damage repair. IFN-gamma, a Th1 cytokine, and TNF-alpha, a pro-inflammatory one, had a central role in the stimulation of cellular and inflammatory reactions. In this study whole blood was collected from five volunteer healthy donors and each donor bag was divided into two satellite bags: one of them was exposed to 137Cs-irradiation with a 2500 cGy dose. Samples for cytokine production, detected by ELISA methods, and proliferative response, evaluated by incorporation of H3 thymidine, were taken at the following storage time: 0, 24, 48, 72 and 96 h. The time-response curve of irradiated mononuclear cells from blood bags (BBMC) in mitogenic activation showed a time-related inhibition of cell proliferation with an enhanced response only after 24 h of storage and about 84% inhibition at 96 h. A similar pattern is follow by IFN-gamma production after OKT3 stimulation. TNF-alpha levels both in lipopolysaccharide stimulated or unstimulated cells were always high. This data suggest that BBMC cells maintain the ability to produce cytokines after gamma-radiation. On the ground of this study seems to be necessary to evaluate hypothetical risk associated with the administration of cytokine via irradiated blood components.
机译:血液产品的伽马射线辐射被认为是预防输血相关的移植物抗宿主疾病的主要手段。先前的研究仅在辐射后一次检测到血液成分中的淋巴细胞抑制率,但是有证据表明在不同的储存时间,细胞因子的产生会引起细胞变异,这可能与辐射活性和细胞损伤修复有关。 IFN-γ(一种Th1细胞因子)和TNF-α(一种促炎细胞)在刺激细胞和炎症反应中起着核心作用。在这项研究中,从五位健康的自愿献血者身上收集了全血,并将每个献血袋分成两个人造卫星袋:其中一个人造卫星暴露于2500CGy剂量的137Cs辐照下。在以下存储时间:0、24、48、72和96 h,通过ELISA方法检测细胞因子产生的样品,并通过掺入H3胸苷评估增殖反应。有丝分裂活化中来自血袋(BBMC)的辐照单核细胞的时间响应曲线显示出与时间相关的细胞增殖抑制,仅在储存24小时后反应增强,在96 h时抑制约84%。 OKT3刺激后产生IFN-γ的情况类似。在脂多糖刺激或未刺激的细胞中,TNF-α水平始终很高。该数据表明,BBMC细胞在γ辐射后仍保持产生细胞因子的能力。基于这项研究,似乎有必要评估通过辐射的血液成分与细胞因子给药相关的假设风险。

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