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首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >Increased production of interleukin-10 and interleukin-1 receptor antagonist after extracorporeal photochemotherapy in chronic graft-versus-host disease.
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Increased production of interleukin-10 and interleukin-1 receptor antagonist after extracorporeal photochemotherapy in chronic graft-versus-host disease.

机译:在慢性移植物抗宿主病的体外光化学疗法后,白细胞介素10和白细胞介素1受体拮抗剂的产生增加。

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BACKGROUND Mechanisms of action of extracorporeal photochemotherapy (ECP) in graft-versus-host disease are incompletely understood. It has been proposed that phagocytosis of apoptotic bodies by monocytes and macrophages induces their activation, a process that increases production of immunosuppressive cytokines. We analyzed apoptosis and cytokine secretion in an autologous coculture system combining peripheral blood lymphocytes (PBL) obtained after ex vivo ECP treatment and nonirradiated peripheral blood mononuclear cells (PBMC).METHODS We studied 11 leukapheresis products treated by ECP from six patients with resistant limited or extensive chronic graft-versus-host disease. Purified PBL obtained by monocyte depletion of the buffy coat from leukapheresis products were mixed with nonirradiated PBMC. Nonirradiated PBL were used as control. Cytokine production was tested at the mRNA level by real-time reverse transcriptase-polymerase chain reaction for interleukin (IL)-10, IL-1 receptor antagonist (IL-1Ra), IL-1beta, tumor necrosis factor-alpha, and IL-12p40.RESULTS Morphologic analysis and flow cytometry displayed important lymphocyte apoptotic features culminating at 24 to 48 hr. Coculture of patient's PBMC with ultraviolet-irradiated PBL as compared with nonirradiated PBL resulted in significant increase of IL-10 mRNA (3418+/-1015 versus 10596+/-3402 mRNA copy numbers; =0.001) and IL-1Ra mRNA (23890+/-6166 versus 41767+/-10181 mRNA copy numbers; =0.001). Incubation with a neutralizing anti-IL-10 monoclonal antibody resulted in a marked decrease of IL-1Ra mRNA levels.CONCLUSION Our findings are consistent with the fact that ECP modifies patient's autologous lymphocytes by inducing a process of apoptosis that activates monocytes and macrophages, leading to increased synthesis of IL-10 and IL-1Ra mRNAs. The induction of this latter mediator is dependent on IL-10.
机译:背景技术体外光化学疗法(ECP)在移植物抗宿主病中的作用机理尚未完全了解。已经提出单核细胞和巨噬细胞对凋亡小体的吞噬作用诱导了它们的活化,这一过程增加了免疫抑制细胞因子的产生。我们分析了自体共培养系统中的细胞凋亡和细胞因子分泌,该系统将离体ECP治疗后获得的外周血淋巴细胞(PBL)与未辐照的外周血单核细胞(PBMC)结合在一起。方法我们研究了6例耐药性有限或耐药的患者经ECP治疗的11种白细胞分离产品广泛的慢性移植物抗宿主病。通过从白细胞分离术产物中去除血沉棕黄层的单核细胞获得的纯化的PBL与未照射的PBMC混合。未照射的PBL用作对照。通过实时逆转录酶-聚合酶链反应检测白介素(IL)-10,IL-1受体拮抗剂(IL-1Ra),IL-1beta,肿瘤坏死因子-α和IL- 12p40。结果形态分析和流式细胞仪显示重要的淋巴细胞凋亡特征在24至48小时达到顶点。与未照射的PBL相比,患者的PBMC与紫外线照射的PBL的共培养导致IL-10 mRNA(3418 +/- 1015与10596 +/- 3402 mRNA的拷贝数; = 0.001)和IL-1Ra mRNA的显着增加(23890 / -6166与41767 +/- 10181 mRNA复制数; = 0.001)。结论:我们的发现与ECP通过诱导激活单核细胞和巨噬细胞的凋亡过程来修饰患者的自体淋巴细胞这一事实相吻合,这一事实与中性抗IL-10单克隆抗体的孵育导致IL-1Ra mRNA水平显着降低。增强IL-10和IL-1Ra mRNA的合成。后一种介体的诱导取决于IL-10。

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