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Human cultured dendritic cells show differential sensitivity to chemotherapy agents as assessed by the MTS assay

机译:通过MTS分析评估,人类培养的树突状细胞对化疗药物的敏感性不同

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Assessment of the chemosensitivity of dendritic cells (DC) may allow more rational development of combined chemotherapy and immunotherapy protocols. Human monocyte-derived DC generated reproducible results in the MTS (Owen’s reagent) assay, which was then used to study DC survival after treatment with four different chemotherapy agents. DC preparations from three different donors were used per drug. DC were sensitive to doxorubicin (concentration range 0.1–50 μM) with variation in sensitivity between donors (IC50 244–1100 nM). The most extreme variation was seen for vinblastine (concentration range 250–0.025 μM with IC50 0.15–17.25 μM). In contrast, there was relative resistance to etoposide (concentration range 0.2–200 μM) and 5-fluorouracil (concentration range 0.7–7700 μM) with no toxicity seen until 50 μM and 770 μM respectively. The function of DC in allogeneic mixed leucocyte reactions closely paralleled results from the MTS assays. The differential sensitivity to chemotherapy agents did not appear to be due to expression of P-glycoprotein. These results suggest that etoposide or 5-fluorouracil is less likely to reduce the immunotherapeutic potential of DC and may be valuable in the design of prodrug activation therapy.
机译:评估树突状细胞(DC)的化学敏感性可以使化学疗法和免疫疗法相结合的方案更加合理。人类单核细胞来源的DC在MTS(欧文试剂)测定中产生可重复的结果,然后用于研究四种不同化疗药物治疗后DC的存活情况。每个药物使用来自三个不同供体的DC制剂。 DC对阿霉素(浓度范围0.1–50μM)敏感,且供体之间的敏感性有所不同(IC50 244–1100 nM)。长春碱的变化最为明显(浓度范围为250–0.025μM,IC50为0.15–17.25μM)。相比之下,对依托泊苷(浓度范围为0.2–200μM)和5-氟尿嘧啶(浓度范围为0.7–7700μM)具有相对抗性,直到50μM和770μM时才观察到毒性。 DC在同种异体混合白细胞反应中的功能与MTS分析的结果非常相似。对化疗药物的敏感性差异似乎不是由于P-糖蛋白的表达所致。这些结果表明依托泊苷或5-氟尿嘧啶不太可能降低DC的免疫治疗潜力,并且在前药活化疗法的设计中可能有价值。

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