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首页> 外文期刊>Journal of Mathematical Biology >A mathematical model for reconstitution of granulopoiesis after high dose chemotherapy with autologous stem cell transplantation
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A mathematical model for reconstitution of granulopoiesis after high dose chemotherapy with autologous stem cell transplantation

机译:自体干细胞移植大剂量化疗后重建粒细胞生成的数学模型

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摘要

High dose chemotherapy supported with hematopoietic progenitor cells gives a characteristic neutropenic period (blood neutrophils <0.5.10(9) c/l) ranging from 10 to 16 days. The question of a correlation between the CFU-GM content of the transplanted CD34+ cells and time to neutrophil recovery by patients having been given high-dose chemotherapy (HD-CT) with stem cell support was addressed by means of a mathematical model of granulopoiesis. The model utilizes a convection-reaction partial differential equation (PDE) with feedback from a cytokine compartment on proliferation, maturation, and mobilization of granulocytes from bone marrow to blood. The observed number of CFU-GM cells in the transplanted CD34+ cell autograft was used as input to the model. Using this approach, the observed gross relationship between CFU-GM content in the reinfused blood product and engraftment time could be reproduced. At the same time, the effects of assumed physiological mechanisms, especially some of the effects of G-CSF on proliferation rate, maturation rate, mobilization, and cell death, could be investigated and discussed relative to observed engraftment. The model makes it possible to explain how cytokines interfere with progenitor cell mobilization from bone marrow to blood, and it points out the implications of a regulating mechanism for the granulocyte maturation rate. [References: 76]
机译:造血祖细胞支持的高剂量化学疗法具有特征性的中性粒细胞减少期(血中性粒细胞<0.5.10(9)c / l),范围为10至16天。已通过粒细胞生成的数学模型解决了移植的CD34 +细胞的CFU-GM含量与接受干细胞支持的大剂量化疗(HD-CT)患者中性粒细胞恢复时间之间的相关性问题。该模型利用对流反应偏微分方程(PDE),并从细胞因子区室反馈粒细胞从骨髓到血液的增殖,成熟和动员。将移植的CD34 +细胞自体移植物中观察到的CFU-GM细胞数量用作模型的输入。使用这种方法,可以重现所观察到的再输注血液制品中CFU-GM含量与植入时间之间的总体关系。同时,可以相对于观察到的移植物研究和讨论假定的生理机制的影响,特别是G-CSF对增殖率,成熟率,动员和细胞死亡的影响。该模型可以解释细胞因子如何干扰祖细胞从骨髓到血液的动员,并指出调节机制对粒细胞成熟率的影响。 [参考:76]

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