ArticleBMC systems biology2013
Merging concepts - coupling an agent-based model of hematopoietic stem cells with an ODE model of granulopoiesis.
Article in BMC systems biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.
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Who cites it
13 citing papers in PubMed.
- Predictive nonlinear modeling of malignant myelopoiesis and tyrosine kinase inhibitor therapy.eLife · 2023Article
- Article
- Optimal experimental design for mathematical models of haematopoiesis.Journal of the Royal Society, Interface · 2021Article
- Calibration, Selection and Identifiability Analysis of a Mathematical Model of the in vitro Erythropoiesis in Normal and Perturbed Contexts.In silico biology · 2019Article
- Transit and lifespan in neutrophil production: implications for drug intervention.Journal of pharmacokinetics and pharmacodynamics · 2018Article
- A stochastic model of myeloid cell lineages in hematopoiesis and pathway mutations in acute myeloid leukemia.PloS one · 2018Article
- Towards Quantitative Systems Pharmacology Models of Chemotherapy-Induced Neutropenia.CPT: pharmacometrics & systems pharmacology · 2017Review
- Response of an oscillatory differential delay equation to a single stimulus.Journal of mathematical biology · 2017Article
- Strategies for efficient numerical implementation of hybrid multi-scale agent-based models to describe biological systems.Cellular and molecular bioengineering · 2015Article
- Multiscale modeling of mucosal immune responses.BMC bioinformatics · 2015Article
- Modelling chemotherapy effects on granulopoiesis.BMC systems biology · 2014Article
- A combined model of human erythropoiesis and granulopoiesis under growth factor and chemotherapy treatment.Theoretical biology & medical modelling · 2014Article
- Computational modeling of heterogeneity and function of CD4+ T cells.Frontiers in cell and developmental biology · 2014Review
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4 authors.
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Abstract
backgroundHematopoiesis is a complex process involving different cell types and feedback mechanisms mediated by cytokines. This complexity stimulated various models with different scopes and applications. A combination of complementary models promises to provide their mutual confirmation and to explain a broader range of scenarios. Here we propose a combination of an ordinary differential equation (ODE) model of human granulopoiesis and an agent-based model (ABM) of hematopoietic stem cell (HSC) organization. The first describes the dynamics of bone marrow cell stages and circulating cells under various perturbations such as G-CSF treatment or chemotherapy. In contrast to the ODE model describing cell numbers, our ABM focuses on the organization of individual cells in the stem population.
resultsWe combined the two models by replacing the HSC compartment of the ODE model by a difference equation formulation of the ABM. In this hybrid model, regulatory mechanisms and parameters of the original models were kept unchanged except for a few specific improvements: (i) Effect of chemotherapy was restricted to proliferating HSC and (ii) HSC regulation in the ODE model was replaced by the intrinsic regulation of the ABM. Model simulations of bleeding, chronic irradiation and stem cell transplantation revealed that the dynamics of hybrid and ODE model differ markedly in scenarios with stem cell damage. Despite these differences in response to stem cell damage, both models explain clinical data of leukocyte dynamics under four chemotherapy regimens.
conclusionsABM and ODE model proved to be compatible and were combined without altering the structure of both models. The new hybrid model introduces model improvements by considering the proliferative state of stem cells and enabling a cell cycle-dependent effect of chemotherapy. We demonstrated that it is able to explain and predict granulopoietic dynamics for a large variety of scenarios such as irradiation, bone marrow transplantation, chemotherapy and growth factor applications. Therefore, it promises to serve as a valuable tool for studies in a broader range of clinical applications, in particular where stem cell activation and proliferation are involved.
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