Hogge Donna E, Feuring-Buske Michaela, Gerhard Brigitte, Frankel Arthur E
Terry Fox Laboratory, British Columbia Cancer Agency, 601 West 10th Avenue, Vancouver, Canada V5Z 1L3.
Leuk Res. 2004 Nov;28(11):1221-6. doi: 10.1016/j.leukres.2004.03.015.
Addition of cytosine arabinoside (Ara-C) to truncated diphtheria toxin (DT388) fused to granulocyte macrophage-colony stimulating factor (GMCSF) or interleukin-3 (IL3) was studied in a NOD/SCID mouse model of human AML. Ara-C alone did not reduce the % human AML cells in mouse bone marrow (BM). DT388IL3 or DT388GMCSF alone reduced but did not eradicate engraftment for two of four and two of three samples, respectively. In contrast, Ara-C with DT388IL3 eliminated AML from mouse BM with one of four samples while DT388GMCSF with Ara-C eliminated or reduced AML cells as compared to mice receiving either agent alone with two of three samples.
在人急性髓系白血病(AML)的NOD/SCID小鼠模型中,研究了将阿糖胞苷(Ara-C)添加到与粒细胞巨噬细胞集落刺激因子(GMCSF)或白细胞介素-3(IL3)融合的截短型白喉毒素(DT388)中。单独使用Ara-C并不能降低小鼠骨髓(BM)中人类AML细胞的百分比。单独使用DT388IL3或DT388GMCSF分别使四个样本中的两个和三个样本中的两个样本的植入减少但未根除。相比之下,Ara-C与DT388IL3联合使用可使四个样本中的一个样本的小鼠BM中的AML消失,而与单独接受任何一种药物的小鼠相比,DT388GMCSF与Ara-C联合使用可使三个样本中的两个样本的AML细胞消失或减少。