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Effects of anticancer agents on cell viability, proliferative activity and cytokine production of peripheral blood mononuclear cells

机译:抗癌药对外周血单个核细胞活力,增殖活性和细胞因子产生的影响

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摘要

We investigated the effects of anticancer agents on peripheral blood mononuclear cells for the purpose of providing data to support new translational chemoimmunotherapy regimens. Peripheral-blood mononuclear cells were treated with one of four anticancer agents (5-fluorouracil, irinotecan, cisplatin, and gemcitabine) for 2 h, after which cell viability was determined. For assessment of effects of each drug on proliferation and cytokine production, cells were stimulated with phytohemagglutinin for 48 h. As a result, the anticancer agents did not affect cell viability. Cell proliferation was unaffected by 5-fluorouracil and irinotecan but inhibited by cisplatin and gemcitabine. Treatment with gemcitabine enhanced the production of IFN-gamma and decreased the number of regulatory T cells. gemcitabine treatment increased IFN-gamma production among CD4 T cells but not among CD8 T cells. The results indicated that GEM had immunoregulatory properties that might support immune response against cancer. This finding has implications for designing chemoimmunotherapy strategies.
机译:我们研究了抗癌药对外周血单个核细胞的作用,目的是提供数据以支持新的翻译化学免疫疗法。用四种抗癌药(5-氟尿嘧啶,伊立替康,顺铂和吉西他滨)之一处理外周血单核细胞2 h,然后测定细胞活力。为了评估每种药物对增殖和细胞因子产生的影响,用植物血凝素刺激细胞48小时。结果,抗癌剂不影响细胞生存力。细胞增殖不受5-氟尿嘧啶和伊立替康的影响,但被顺铂和吉西他滨抑制。用吉西他滨治疗可增强IFN-γ的产生,并减少调节性T细胞的数量。吉西他滨治疗增加了CD4 T细胞中的IFN-γ产生,但没有增加CD8 T细胞中的IFN-γ产生。结果表明,GEM具有免疫调节特性,可能支持针对癌症的免疫反应。该发现对设计化学免疫疗法策略具有启示。

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