rhG-CSF对健康供者外周血及骨髓免疫特性影响比较.docVIP

rhG-CSF对健康供者外周血及骨髓免疫特性影响比较.doc

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rhG-CSF对健康供者外周血及骨髓免疫特性影响比较

rhG-CSF对健康供者外周血及骨髓免疫特性影响比较   作者:赵翔宇,常英军,黄晓军 【摘要】   本研究探讨rhG-CSF对健康供者外周血采集物(G-PB)和骨髓采集物(G-BM)免疫学特性影响的异同。用MTT法和夹心酶联免疫复合物(ELISA)法检测G-PB和G-BM中T淋巴细胞增殖能力和IL-4、IFN-γ的分泌,并用流式细胞术测定两种移植物的T细胞亚群、树突状细胞(DC)亚群、单核细胞及共刺激分子CD28的表达。结果表明: G-PB中淋巴细胞,CD3+、CD4+、CD8+ T淋巴细胞,DC1、DC2以及单核细胞的含量,CD4/CD8的比值高于G-BM(P<0.001)。G-PB的T淋巴细胞增殖能力高于G-BM(P<0.05);每微升G-PB移植物中T淋巴细胞分泌细胞因子IFN-γ、IL-4的量均明显高于G-BM,且G-PB中IL-4/IFN-γ比值小于G-BM(P<0001),DC2与T淋巴细胞的比值也低于G-BM(P<0.01);而G-PB中CD4+、CD8+细胞上CD28表达的百分比和总体表达均高于G-BM(P<0001)。结论: rhG-CSF体内应用诱导G-PB和G-BM产生的T细胞免疫低反应性是有差异的,而两者之间的差异是G-PB和G-BM移植后移植物抗宿主病(GVHD)发生率和程度不同的免疫学基础。 【关键词】 粒细胞集落刺激因子;外周血移植物;骨髓移植物;共刺激分子;免疫低反应性   Effects of rhG-CSF Mobilization on Immunological Properties of Grafts from Peripheral Blood and Bone Marrow   Abstract This study was aimed to investigate the difference of immunological properties between recombination human granulocyte colony-stimulating factor (rhG-CSF) mobilized peripheral blood grafts (G-PB) and rhG-CSF primed bone marrow grafts (G-BM).The lymphocyte proliferation ability and the quantities of interleukin-4 (IL-4) and interfe-ron-γ (IFN-γ) secreted by T cells were determined by using MTT assays and sandwich ELISA; T cell subgroups,dendritic cells (DC),monocytes and the expression of CD28 costimulatory molecules on T cells were determined by multicolor flow cytometry. The results showed that the absolute numbers of lymphocytes,monocytes,CD3+,CD4+ and CD8+ T cells as well as DC1 and DC2,the ratios of CD4/CD8 in G-PB were significantly higher than those in G-BM,respectively (P<0.001). T cell proliferation ability was significantly higher in G-PB than that in G-BM (P<0.05). The quantities of IFN-γ and IL-4 secreted by T cells per micromilter of G-PB was significantly higher than those of G-BM,the ratios of IL-4/IFN-γ were significantly lower in G-PB than that in G-BM (P<0.001). As compared with G-BM,the ratio between DC2 and T-lymphocyte was significantly low in G-PB (P<0.01),whereas the percentage and overall expression of CD28 on CD4+ and C

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