...
首页> 外文期刊>Cancer Cell International >Granulocyte-macrophage stimulating factor (GM-CSF) increases circulating dendritic cells but does not abrogate suppression of adaptive cellular immunity in patients with metastatic colorectal cancer receiving chemotherapy
【24h】

Granulocyte-macrophage stimulating factor (GM-CSF) increases circulating dendritic cells but does not abrogate suppression of adaptive cellular immunity in patients with metastatic colorectal cancer receiving chemotherapy

机译:接受化疗的转移性结直肠癌患者中的粒细胞巨噬细胞刺激因子(GM-CSF)可增加循环树突状细胞,但不会消除对适应性细胞免疫的抑制作用

获取原文
           

摘要

Background Advanced cancer and chemotherapy are both associated with immune system suppression. We initiated a clinical trial in patients receiving chemotherapy for metastatic colorectal cancer to determine if administration of GM-CSF in this setting was immunostimulatory. Methods Between June, 2003 and January, 2007, 20 patients were enrolled in a clinical trial (NCT00257322) in which they received 500 ug GM-CSF daily for 4 days starting 24 hours after each chemotherapy cycle. There were no toxicities or adverse events reported. Blood was obtained before chemotherapy/GM-CSF administration and 24 hours following the final dose of GM-CSF and evaluated for circulating dendritic cells and adaptive immune cellular subsets by flow cytometry. Peripheral blood mononuclear cell (PBMC) expression of γ-interferon and T-bet transcription factor (Tbx21) by quantitative real-time PCR was performed as a measure of Th1 adaptive cellular immunity. Pre- and post-treatment (i.e., chemotherapy and GM-CSF) samples were evaluable for 16 patients, ranging from 1 to 5 cycles (median 3 cycles, 6 biologic sample time points). Dendritic cells were defined as lineage (-) and MHC class II high (+). Results 73% of patients had significant increases in circulating dendritic cells of ~3x for the overall group (5.8% to 13.6%, p = 0.02) and ~5x excluding non-responders (3.2% to 14.5%, p Tbx21 levels declined by 75% following each chemotherapy cycle despite administration of GM-CSF (p = 0.02). PBMC γ-interferon expression, however was unchanged. Conclusions This clinical trial confirms the suppressive effects of chemotherapy on Th1 cellular immunity in patients with metastatic colorectal cancer but demonstrates that mid-cycle administration of GM-CSF can significantly increase the proportion of circulating dendritic cells. As the role of dendritic cells in anti-tumor immunity becomes better defined, GM-CSF administration may provide a non-toxic intervention to augment this arm of the immune system for cancer patients receiving cytotoxic therapy. Trial Registration ClinicalTrials.gov: NCT00257322
机译:背景技术晚期癌症和化学疗法均与免疫系统抑制有关。我们在接受化疗的转移性结直肠癌患者中启动了一项临床试验,以确定在这种情况下施用GM-CSF是否具有免疫刺激性。方法在2003年6月至2007年1月之间,有20名患者参加了一项临床试验(NCT00257322),其中他们在每个化疗周期后的24小时开始每天接受500 ug GM-CSF,共4天。没有毒性或不良反应的报道。在化疗/ GM-CSF给药之前和最终剂量的GM-CSF后24小时获得血液,并通过流式细胞术评估循环树突状细胞和适应性免疫细胞亚群。通过定量实时PCR进行γ-干扰素和T-bet转录因子(Tbx21)的外周血单个核细胞(PBMC)表达,以作为Th1适应性细胞免疫的量度。治疗前后(即化疗和GM-CSF)样品可评估16例患者,范围为1至5个周期(中位3个周期,6个生物学样品时间点)。树突状细胞定义为谱系(-)和II类MHC高(+)。结果总体组中73%的患者循环树突状细胞显着增加,约为3倍(5.8%至13.6%,p = 0.02),排除无反应者则约为5x(3.2%至14.5%,p Tbx21水平下降了75%)尽管给予了GM-CSF,每个化疗周期后的百分率(p = 0.02),但是PBMCγ-干扰素的表达没有变化结论结论该临床试验证实了化疗对转移性结直肠癌患者Th1细胞免疫的抑制作用,但证明了这一点。 GM-CSF的中期周期给药可显着增加循环树突状细胞的比例,随着树突状细胞在抗肿瘤免疫中的作用得到更好的界定,GM-CSF给药可提供无毒干预以增强该树突状细胞的这一分支。接受细胞毒素治疗的癌症患者的免疫系统。临床注册ClinicalTrials.gov:NCT00257322

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号