Talpaz M, Spitzer G, Hittelman W, Kantarjian H, Gutterman J
Exp Hematol. 1986 Aug;14(7):668-71.
Myeloid cytoreduction leading to hematologic remissions is frequently seen among patients with chronic phase Philadelphia-positive chronic myelogenous leukemia (CML Ph') treated with leukocyte interferon (IFN-alpha). In order extend our understanding of the events associated with interferon-induced myeloid cytoreductions, we have examined the changes in granulocyte-monocyte colony-forming cells (GM-CFC) in such CML Ph' patients. A total of 28 CML Ph' patients in hematologic remissions following IFN-alpha treatment had a median GM-CFC of 12 (range, 0-182)/1 X 10(5) bone marrow cells. This was significantly lower than the median GM-CFC of 104 (range, 44-815; p less than 0.01) in 22 untreated or minimally treated CML Ph' patients and the median of 72 (range, 30-204; p less than 0.05) in 18 normal controls. A gradual decline in the GM-CFC numbers from a median of 105 to a median of 1.8 was seen in six responding patients who were studied serially over a median period of 7.5 months. In these patients, we also observed a profound decline in the number of aspirated bone marrow nucleated cells and a decline in the bone marrow cellularity. The effect of treatment interruption for a median of 13 days was studied in five patients. In three of the patients who had received IFN-alpha for less than or equal to 6 months, treatment interruption resulted in rapid increase in the GM-CFC, while the GM-CFC did not change in the remaining two patients, who received IFN-alpha for one and two years. We conclude that treatment of CML patients with IFN-alpha resulted in a progressive decline of the bone marrow GM-CFC. The initially expanded pool of committed myeloid stem cells declines gradually, and at the time of hematologic remission the number of GM-CFC/10(5) nucleated bone marrow cells is lower than that of normal controls. In the early phases of IFN-alpha treatment, this inhibitory effect is rapidly reversible, but it seems to persist when the treatment is extended over more than one year.
在接受白细胞干扰素(IFN-α)治疗的慢性期费城染色体阳性慢性髓性白血病(CML Ph')患者中,常可见到导致血液学缓解的髓系细胞减少。为了进一步了解与干扰素诱导的髓系细胞减少相关的事件,我们研究了此类CML Ph'患者中粒细胞 - 单核细胞集落形成细胞(GM-CFC)的变化。总共28例接受IFN-α治疗后处于血液学缓解期的CML Ph'患者,其GM-CFC的中位数为12(范围0 - 182)/1×10⁵骨髓细胞。这显著低于22例未治疗或仅接受少量治疗的CML Ph'患者的GM-CFC中位数104(范围44 - 815;p < 0.01)以及18例正常对照的中位数72(范围30 - 204;p < 0.05)。在中位时间为7.5个月内对6例有反应的患者进行连续研究,发现GM-CFC数量从中位数105逐渐下降至中位数1.8。在这些患者中,我们还观察到抽取的骨髓有核细胞数量显著减少以及骨髓细胞密度降低。对5例患者进行了中位时间为13天的治疗中断效果研究。在3例接受IFN-α治疗时间小于或等于6个月的患者中,治疗中断导致GM-CFC迅速增加,而在另外2例分别接受IFN-α治疗1年和2年的患者中,GM-CFC没有变化。我们得出结论,IFN-α治疗CML患者会导致骨髓GM-CFC逐渐减少。最初扩增的定向髓系干细胞池逐渐下降,在血液学缓解时,GM-CFC/10⁵有核骨髓细胞数量低于正常对照。在IFN-α治疗的早期阶段,这种抑制作用可迅速逆转,但当治疗延长超过一年时,这种抑制作用似乎会持续存在。