Haworth C, O'Reilly S M, Chu E, Rustin G J, Feldmann M
Charing Cross Sunley Research Centre, London, UK.
Br J Cancer. 1993 Jun;67(6):1346-50. doi: 10.1038/bjc.1993.249.
Twelve patients undergoing IL-2 and flavone acetic acid (FAA) combination immunotherapy for advanced melanoma were studied throughout treatment for the induction of measurable levels of bioactive TNF, GM-CSF and IL-6 in their serum. This was to assess the extent of secondary cytokine induction in these patients and the possible role of such cytokines in both the toxic and therapeutic responses. The nature of the treatment schedule enabled these cytokines to be measured in response to FAA alone, FAA/IL-2 and FAA alone following IL-2/FAA activation of target cells. A small rise in the serum levels of these cytokines was seen on the initial course of FAA/IL-2 but this was minor compared to the marked elevation in levels 2-8 h following the initiation of the third course of FAA given with or without IL-2 and at a time point which coincided with maximum toxicity in those patients who experienced it. These results show that FAA alone can induce cytokine release from primed target cells. This may be associated with the therapeutic effect and/or toxicity of the agent.
对12例接受白细胞介素-2(IL-2)和黄酮醋酸(FAA)联合免疫疗法治疗晚期黑色素瘤的患者在整个治疗过程中进行了研究,以诱导其血清中可测量水平的生物活性肿瘤坏死因子(TNF)、粒细胞-巨噬细胞集落刺激因子(GM-CSF)和白细胞介素-6(IL-6)。这是为了评估这些患者中继发性细胞因子诱导的程度以及此类细胞因子在毒性反应和治疗反应中可能发挥的作用。治疗方案的性质使得能够在单独使用FAA、FAA/IL-2以及在IL-2/FAA激活靶细胞后单独使用FAA的情况下测量这些细胞因子。在FAA/IL-2的初始疗程中,这些细胞因子的血清水平出现了小幅上升,但与在给予或未给予IL-2的情况下开始第三疗程FAA后2 - 8小时水平的显著升高相比,这一上升幅度较小,且该时间点与出现毒性反应的患者的最大毒性时间点一致。这些结果表明,单独使用FAA可诱导致敏靶细胞释放细胞因子。这可能与该药物的治疗效果和/或毒性有关。