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首页> 外文期刊>Oncology: International Journal of Cancer Research and Treatment >Chemotherapy ± cetuximab modulates peripheral immune responses in metastatic colorectal cancer
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Chemotherapy ± cetuximab modulates peripheral immune responses in metastatic colorectal cancer

机译:化学疗法±西妥昔单抗调节转移性结直肠癌的外周免疫反应

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摘要

Objective: To identify changes in peripheral immune responses in patients with metastatic colorectal cancer (mCRC) treated with irinotecan/5-fluorouracil/ leucovorin (IFL) alone or in combination with cetuximab (C-IFL). Methods: Peripheral blood mononuclear cells (PBMCs) collected from healthy donors (n = 20) and patients with mCRC receiving treatment with either IFL (n = 30) or C-IFL (n = 30) were tested for cytokine production upon polyclonal stimulation with anti-CD3 monoclonal antibody, T cell proliferation in the autologous mixed lymphocyte reaction (auto-MLR) and T regulatory cell (Treg) frequency. The respective results were evaluated over two treatment cycles and further assessed in relation to response to treatment. Results: PBMCs prior to treatment exhibited significantly lower production of IL-2, IFN-γ, IL-12 and IL-18 cytokines and lower auto-MLR responses, whereas Treg frequency, IL-4, IL-10 cytokines were increased compared to healthy donors. During treatment, IL-2, IFN-γ, IL-12, IL-18 and auto-MLR responses increased, while Treg frequency and IL-10 secretion decreased significantly compared to the baseline. Responders to treatment exhibited a significantly higher increase in IL-2, IFN-γ, IL-12 and IL-18 production and auto-MLR responses, and higher decrease in IL-4, IL-10 secretion and Treg frequency. Among all patient subgroups analysed, responders to C-IFL demonstrated significantly higher increase in auto-MLR responses, IL-12 and IL-18 secretion and higher decrease in Treg frequency. Conclusion: The disturbed immune parameters observed in patients with mCRC at presentation can be significantly improved during treatment with IFL and this effect can be potentiated by the addition of cetuximab. Monitoring of the peripheral immune system function could be used as surrogate marker in predicting treatment-related outcome.
机译:目的:确定单独或联合西妥昔单抗(C-IFL)的伊立替康/ 5-氟尿嘧啶/亚叶酸钙(IFL)治疗的转移性结直肠癌(mCRC)患者外周免疫反应的变化。方法:测试从健康供体(n = 20)和接受IFL(n = 30)或C-IFL(n = 30)治疗的mCRC患者的外周血单个核细胞(PBMC)在多克隆刺激下的细胞因子产生。抗CD3单克隆抗体时,T细胞在自体混合淋巴细胞反应中的增殖(auto-MLR)和T调节细胞(Treg)的频率有关。在两个治疗周期中评估了各自的结果,并进一步评估了对治疗的反应。结果:治疗前的PBMC表现出明显降低的IL-2,IFN-γ,IL-12和IL-18细胞因子的产生以及更低的自身MLR反应,而与之相比,Treg频率,IL-4,IL-10细胞因子增加了健康的捐助者。在治疗期间,与基线相比,IL-2,IFN-γ,IL-12,IL-18和自身MLR反应增加,而Treg频率和IL-10分泌显着减少。对治疗的反应者表现出IL-2,IFN-γ,IL-12和IL-18产生以及自身MLR反应显着更高的增加,以及IL-4,IL-10分泌和Treg频率的显着降低。在所有分析过的患者亚组中,对C-IFL的应答者表现出自体MLR应答,IL-12和IL-18分泌显着更高的增加以及Treg频率的更大降低。结论:IFL治疗期间,可显着改善mCRC患者在就诊时观察到的免疫参数紊乱,并且西妥昔单抗的加入可增强这种作用。外周免疫系统功能的监测可用作预测治疗相关结果的替代指标。

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