Hirt A, Schmid A M, Luethy A R, Gugler E, Wagner H P
Department of Pediatrics (Inselspital), University of Berne, Switzerland.
Exp Hematol. 1990 Jan;18(1):37-40.
In children with acute lymphoblastic leukemia (ALL), megakaryocytopoiesis was investigated in vitro by the semisolid agar culture technique. In untreated ALL the median number of committed megakaryocyte progenitor cells (CFU-Mk) in the bone marrow was 2 (range less than 0.1-8) per 10(5) bone marrow cells instead of 30 (range 14-93) in controls, the impairment being dependent on the degree of leukemic bone marrow infiltration. However, if the number of CFU-Mk was related to residual nonleukemic bone marrow cells only, two-thirds of the children investigated had a frequency of CFU-Mk within the normal range. After 2 weeks of induction therapy the majority of the children had a low number of CFU-Mk in the bone marrow (median 6, range 0.5-40), a fact that could no longer be explained by a dilution of CFU-Mk by leukemic cells. After 4 weeks of chemotherapy (day 29) the frequency of CFU-Mk had risen to 18 (range 3-67) per 10(5) bone marrow cells, a value still significantly (p less than 0.01) below the normal range. In contrast to the changes in the number of CFU-Mk the median cell number per megakaryocyte colony remained constant during induction of remission. After cessation of long-term chemotherapy all children investigated had a normal number of CFU-Mk, suggesting that no permanent chemotherapy-related damage to committed megakaryocyte progenitor cells was induced.
采用半固体琼脂培养技术对急性淋巴细胞白血病(ALL)患儿的巨核细胞生成进行了体外研究。在未经治疗的ALL患儿中,每10⁵个骨髓细胞中定向巨核细胞祖细胞(CFU-Mk)的中位数为2(范围小于0.1 - 8),而对照组为30(范围14 - 93),这种损害取决于白血病骨髓浸润的程度。然而,如果仅将CFU-Mk的数量与残留的非白血病骨髓细胞相关联,那么三分之二的受试儿童CFU-Mk频率在正常范围内。诱导治疗2周后,大多数患儿骨髓中的CFU-Mk数量较低(中位数为6,范围0.5 - 40),这一事实不能再用白血病细胞对CFU-Mk的稀释来解释。化疗4周后(第29天),CFU-Mk的频率升至每10⁵个骨髓细胞18(范围3 - 67),该值仍显著(p < 0.01)低于正常范围。与CFU-Mk数量的变化相反,在诱导缓解期间每个巨核细胞集落的细胞中位数保持不变。长期化疗停止后,所有受试儿童的CFU-Mk数量均正常,这表明未诱导产生与化疗相关的对定向巨核细胞祖细胞的永久性损害。