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体外光化学疗法影响移植物抗宿主病患者树突状细胞共刺激分子的表达及白细胞介素-10的产生。

Extracorporeal photopheresis affects co-stimulatory molecule expression and interleukin-10 production by dendritic cells in graft-versus-host disease patients.

作者信息

Di Renzo M, Sbano P, De Aloe G, Pasqui A L, Rubegni P, Ghezzi A, Auteri A, Fimiani M

机构信息

Azienda Ospedaliera Universitaria Senese, University of Siena, Siena, Italy.

出版信息

Clin Exp Immunol. 2008 Mar;151(3):407-13. doi: 10.1111/j.1365-2249.2007.03577.x.

Abstract

Graft-versus-host disease (GVHD) is a major complication of allogeneic bone marrow transplantation. Extracorporeal photochemotherapy (ECP) has been introduced as an alternative treatment for GVHD refractory to conventional immunosuppressive treatment, although its mechanism of action is not yet clear. We investigated, in seven GVHD patients, the effects of ECP on dendritic cell maturation and cytokine production in an in vitro model that could mimic the potential in vivo effect of reinfusion of ECP-treated peripheral blood mononuclear cells. The model was based on co-culture of ECP-treated lymphocytes with monocyte-derived dendritic cells (DCs) of the same patient. We found that the co-culture of ECP-treated lymphocytes with immature DCs reduced CD54, CD40 and CD86 mean fluorescence intensity (MFI) significantly after lipopolysaccharide (LPS) stimulation, without affecting human leucocyte antigen D-related and CD80 MFI. In the same co-culture model, DCs produced increased amounts of interleukin (IL)-10 when co-cultured with ECP-treated lymphocytes and stimulated with LPS, while IL-12 and tumour necrosis factor-alpha production were not affected. These results suggest that reinfusion of large numbers of autologous apoptotic lymphocytes is significant for the therapeutic outcome of ECP through down-regulation of co-stimulatory molecules on DCs, inducing non-fully mature DCs with a low signal 2 and up-regulation of IL-10, which is an immunosuppressive cytokine.

摘要

移植物抗宿主病(GVHD)是同种异体骨髓移植的主要并发症。体外光化学疗法(ECP)已被引入作为常规免疫抑制治疗难治的GVHD的替代治疗方法,尽管其作用机制尚不清楚。我们在7例GVHD患者中,在一个能够模拟ECP处理的外周血单个核细胞再输注的潜在体内效应的体外模型中,研究了ECP对树突状细胞成熟和细胞因子产生的影响。该模型基于将ECP处理的淋巴细胞与同一患者的单核细胞衍生树突状细胞(DC)共培养。我们发现,在脂多糖(LPS)刺激后,ECP处理的淋巴细胞与未成熟DC的共培养显著降低了CD54、CD40和CD86的平均荧光强度(MFI),而不影响人类白细胞抗原D相关分子和CD80的MFI。在同一共培养模型中,当与ECP处理的淋巴细胞共培养并用LPS刺激时,DC产生的白细胞介素(IL)-10量增加,而IL-12和肿瘤坏死因子-α的产生不受影响。这些结果表明,大量自体凋亡淋巴细胞的再输注对于ECP的治疗效果具有重要意义,其通过下调DC上的共刺激分子,诱导具有低信号2的未完全成熟DC,并上调作为免疫抑制细胞因子的IL-10。

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