Findley H W, Kennedy M S, Lui V K, Ragab A H
Exp Hematol. 1979 Nov;7(10):495-9.
Acute lymphoblastic leukemia (ALL) in children is often characterized by defective granulopoiesis during initial and relapse stages of the disease, resulting in absolute neutropenia in vivo and in low or absent production of granulocyte-macrophage colonies in vitro. The purpose of this study was to determine if leukemic lymphoblasts from untreated ALL patients could inhibit normal granulopoiesis. Several concentrations of leukemic bone marrow cells from nine patients were mixed with either normal bone marrow cells or with autologous (HLA-identical) remission bone marrow cells, incubated for 1 hour, and co-cultured by the double layer agar technique. The cells were also cultured separately as controls. No statistically significant differences occurred between observed and expected colony counts in the majority of experiments. With three patients, slight inhibition occurred at some but not all leukemic cell concentrations tested; this inhibition was not correlated with the leukemic cell concentration. These results indicate that leukemic cells from untreated ALL patients do not significantly inhibit normal in vitro granulopoiesis at the committed stem cell level or at later levels of differentiation; therefore, such inhibition does not appear to be responsible for ALL-associated neutropenia.
儿童急性淋巴细胞白血病(ALL)在疾病的初始阶段和复发阶段通常以粒细胞生成缺陷为特征,导致体内绝对中性粒细胞减少,体外粒细胞 - 巨噬细胞集落生成减少或缺乏。本研究的目的是确定未经治疗的ALL患者的白血病原始淋巴细胞是否能抑制正常的粒细胞生成。将来自9名患者的几种浓度的白血病骨髓细胞与正常骨髓细胞或自体(HLA相同)缓解期骨髓细胞混合,孵育1小时,然后通过双层琼脂技术进行共培养。细胞也分别作为对照进行培养。在大多数实验中,观察到的集落数与预期集落数之间没有统计学上的显著差异。有3名患者,在某些但不是所有测试的白血病细胞浓度下出现了轻微抑制;这种抑制与白血病细胞浓度无关。这些结果表明,未经治疗的ALL患者的白血病细胞在定向干细胞水平或后期分化水平上不会显著抑制正常的体外粒细胞生成;因此,这种抑制似乎不是ALL相关中性粒细胞减少的原因。