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Changes of T-lymphocyte subpopulation and differential expression pattern of the T-bet and GATA-3 genes in diffuse large B-cell lymphoma patients after chemotherapy

机译:弥漫性大B细胞淋巴瘤患者化疗后T淋巴细胞亚群的变化及T-bet和GATA-3基因的差异表达模式

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T cell-mediated immunity plays an important role in enhancing antitumor response.This study aimed to investigate the changes in the T-lymphocyte subpopulation and to characterize the differential expression pattern of corresponding regulatory genes in peripheral blood mononuclear cells (PBMCs) from diffuse large B cell lymphoma (DLBCL) patients before and after chemotherapy. A total of 56 DLBCL patients were recruited for analysis of T-cell subset distribution in the peripheral blood using flow cytometry; serum interferon (IFN)-γ and interleukin (IL)-4 levels using enzyme-linked immunosorbent assays; and early growth response protein 1 (EGR-1), T-bet, GATA-binding protein 3 (GATA-3), and transforming growth factor (TGF)-β mRNA levels using quantitative reverse-transcription polymerase chain reaction. Twenty-six healthy subjects served as controls. The percentage of CD3+CD4+T lymphocytes in peripheral blood from DLBCL patients was significantly decreased, whereas the percentages of CD3+CD8+T and CD4+CD25+T cells were significantly increased compared to those in controls (p < 0.05). Serum levels of IFN-γ and IL-4 were also significantly lower in DLBCL patients than those in controls (p < 0.05), and the levels of EGR-1, T-bet, and GATA-3 mRNA in PBMCs were lower (2.69 ± 1.48, 9.43 ± 2.14, and 20.83 ± 9.05 fold, respectively) in DLBCL patients than those in controls. Furthermore, there was a positive association between the levels of EGR-1 and T-bet mRNA (p = 0.001). However, the level of TGF-β mRNA was significantly increased in DLBCL patients, which was inversely associated with the T-bet mRNA level (p = 0.008), but positively associated with the percentage of T regulatory cells in PBMCs (p = 0.011). After three cycles of chemotherapy, the distribution of T-lymphocyte subsets in DLBCL patients were changed, and the levels of EGR-1, T-bet, and GATA-3 mRNA were significantly increased (p < 0.05) compared to those before chemotherapy. These results demonstrate the changes in T-lymphocyte subpopulations and the altered expression 34 pattern of the corresponding regulatory genes in PBMCs from DLBCL patients after chemotherapy, which are associated with the response of patients to treatment. The preferential expression of the T-bet gene after chemotherapy was closely correlated with the increased expression of the EGR-1 gene and decreased expression of the TGF-β gene.
机译:T细胞介导的免疫在增强抗肿瘤反应中起着重要作用。本研究旨在研究T淋巴细胞亚群的变化,并表征弥漫性大B细胞外周血单个核细胞(PBMC)中相应调节基因的差异表达模式。化疗前后的细胞淋巴瘤(DLBCL)患者。总共招募了56名DLBCL患者,以流式细胞术分析外周血T细胞亚群的分布。使用酶联免疫吸附法测定血清干扰素(IFN)-γ和白介素(IL)-4水平;使用定量逆转录聚合酶链反应检测早期生长反应蛋白1(EGR-1),T-bet,GATA结合蛋白3(GATA-3)和转化生长因子(TGF)-βmRNA水平。 26名健康受试者作为对照。与对照组相比,DLBCL患者外周血中CD3 + CD4 + T淋巴细胞的百分比显着降低,而CD3 + CD8 + T和CD4 + CD25 + T细胞的百分比则显着增加(p <0.05)。 DLBCL患者的血清IFN-γ和IL-4水平也显着低于对照组(p <0.05),PBMC中EGR-1,​​T-bet和GATA-3 mRNA的水平较低(2.69)在DLBCL患者中,相对于对照组,分别为±1.48、9.43±2.14和20.83±9.05倍。此外,EGR-1和T-bet mRNA的水平呈正相关(p = 0.001)。然而,DLBCL患者的TGF-βmRNA水平显着升高,与T-bet mRNA水平呈负相关(p = 0.008),但与PBMC中T调节细胞的百分比呈正相关(p = 0.011) 。经过三个化疗周期后,DLBCL患者的T淋巴细胞亚群的分布发生了变化,与化疗前相比,EGR-1,​​T-bet和GATA-3 mRNA的水平显着增加(p <0.05)。这些结果证明了来自DLBCL患者的PBMC中化疗后T淋巴细胞亚群的变化和相应调节基因的表达34模式的改变,这与患者对治疗的反应有关。化疗后T-bet基因的优先表达与EGR-1基因表达的增加和TGF-β基因表达的减少密切相关。

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