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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的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-γ and decreased the number of regulatory T cells. gemcitabine treatment increased IFN-γ 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性化学免疫治疗方案。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小时,然后确定细胞活力。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加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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