Grossmann A, Lenox J, Deisher T A, Ren H P, Humes J M, Kaushansky K, Sprugel K H
ZymoGenetics Inc, Seattle, WA 98102-3702, USA.
Blood. 1996 Nov 1;88(9):3363-70.
Severe suppression of the hematopoietic system is a major factor in limiting chemotherapy dose escalation. To determine whether a combination of human recombinant granulocyte colony-stimulating factor (G-CSF) and thrombopoietin (TPO) would alter recovery of platelets, red blood cells (RBCs), or neutrophils after myeloablative therapy, myelosuppressed mice were treated with sc injections of TPO (90 micrograms/kg), G-CSF (250 micrograms/kg). TPO plus G-CSF or vehicle and complete blood counts were measured. Marrow and spleen cells were obtained at various times and assayed for erythroid, myeloid, and megakaryocytic progenitors. The prolonged neutropenia in vehicle controls (14 days) was significantly shortened in mice treated with G-CSF or TPO for 14 days. The combination of TPO plus G-CSF further reduced the duration of neutropenia. TPO and TPO plus G-CSF treatments also significantly shortened thrombocytopenia compared to vehicle. Recovery of RBCs was also enhanced in mice treated with either G-CSF or TPO, or the combination. Furthermore, treatment with G-CSF and/or TPO hastened myeloid, erythroid, and megakaryocyte progenitor recovery compared to vehicle controls. These results show that the combination of TPO plus G-CSF acts synergistically to accelerate neutrophil recovery in myelosuppressed mice and does not compromise the platelet or RBC response to TPO therapy.
造血系统的严重抑制是限制化疗剂量增加的主要因素。为了确定重组人粒细胞集落刺激因子(G-CSF)和血小板生成素(TPO)联合使用是否会改变清髓治疗后血小板、红细胞(RBC)或中性粒细胞的恢复情况,对骨髓抑制小鼠皮下注射TPO(90微克/千克)、G-CSF(250微克/千克)进行治疗。测量TPO加G-CSF或赋形剂以及全血细胞计数。在不同时间获取骨髓和脾细胞,并检测红系、髓系和巨核系祖细胞。在赋形剂对照组中持续时间较长的中性粒细胞减少症(14天),在用G-CSF或TPO治疗14天的小鼠中显著缩短。TPO加G-CSF的联合使用进一步缩短了中性粒细胞减少症的持续时间。与赋形剂相比,TPO以及TPO加G-CSF治疗也显著缩短了血小板减少症的持续时间。在用G-CSF或TPO或两者联合治疗的小鼠中,RBC的恢复也得到增强。此外,与赋形剂对照组相比,用G-CSF和/或TPO治疗可加速髓系、红系和巨核系祖细胞的恢复。这些结果表明,TPO加G-CSF联合使用具有协同作用,可加速骨髓抑制小鼠中性粒细胞的恢复,且不会损害血小板或RBC对TPO治疗的反应。