Chachoua A, Oratz R, Hoogmoed R, Caron D, Peace D, Liebes L, Blum R H, Vilcek J
Kaplan Cancer Center, Division of Medical Oncology, New York University Medical Center, New York 10016.
J Immunother Emphasis Tumor Immunol. 1994 Apr;15(3):217-24. doi: 10.1097/00002371-199404000-00008.
Twenty-four patients with solid malignancies were treated with granulocyte-macrophage colony-stimulating factor (GM-CSF) on a Phase 1b trial. The objective of the study was to evaluate the effects of GM-CSF on peripheral blood monocyte activation. GM-CSF was administered by subcutaneous injection daily for 14 days. Immune parameters measured were monocyte cytotoxicity against the human colon carcinoma (HT29) cell line, serum tumor necrosis factor (TNF)-alpha, interleukin (IL)-1 beta, and in vitro TNF-alpha and IL-1 beta induction. All patients were evaluable for toxicity. Fifteen patients were evaluable for immunologic response. Treatment with GM-CSF led to a statistically significant enhancement in direct monocyte cytotoxicity against HT29 cells. There was no increase in serum TNF-alpha or IL-1 beta and no consistent in vitro induction of TNF-alpha or IL-1 beta from monocytes posttreatment. Treatment was well tolerated overall. We conclude that treatment with GM-CSF can lead to enhanced monocyte cytotoxicity. Further studies are in progress to evaluate the effect of GM-CSF on other parameters of monocyte functions.
24例实体恶性肿瘤患者在1b期试验中接受了粒细胞巨噬细胞集落刺激因子(GM-CSF)治疗。该研究的目的是评估GM-CSF对外周血单核细胞活化的影响。GM-CSF通过皮下注射每日给药,持续14天。检测的免疫参数包括单核细胞对人结肠癌细胞系(HT29)的细胞毒性、血清肿瘤坏死因子(TNF)-α、白细胞介素(IL)-1β以及体外TNF-α和IL-1β诱导情况。所有患者均可评估毒性。15例患者可评估免疫反应。GM-CSF治疗导致对HT29细胞的直接单核细胞细胞毒性有统计学意义的增强。血清TNF-α或IL-1β没有增加,治疗后单核细胞体外也没有一致的TNF-α或IL-1β诱导。总体而言,治疗耐受性良好。我们得出结论,GM-CSF治疗可导致单核细胞细胞毒性增强。正在进行进一步研究以评估GM-CSF对单核细胞功能其他参数的影响。