Clonal Dominance and Transplantation Dynamics in Hematopoietic Stem Cell Compartments
Overview
Affiliations
Hematopoietic stem cells in mammals are known to reside mostly in the bone marrow, but also transitively passage in small numbers in the blood. Experimental findings have suggested that they exist in a dynamic equilibrium, continuously migrating between these two compartments. Here we construct an individual-based mathematical model of this process, which is parametrised using existing empirical findings from mice. This approach allows us to quantify the amount of migration between the bone marrow niches and the peripheral blood. We use this model to investigate clonal hematopoiesis, which is a significant risk factor for hematologic cancers. We also analyse the engraftment of donor stem cells into non-conditioned and conditioned hosts, quantifying the impact of different treatment scenarios. The simplicity of the model permits a thorough mathematical analysis, providing deeper insights into the dynamics of both the model and of the real-world system. We predict the time taken for mutant clones to expand within a host, as well as chimerism levels that can be expected following transplantation therapy, and the probability that a preconditioned host is reconstituted by donor cells.
Stiehl T Front Immunol. 2024; 15:1321336.
PMID: 39737169 PMC: 11682905. DOI: 10.3389/fimmu.2024.1321336.
Modelling post-chemotherapy stem cell dynamics in the bone marrow niche of AML patients.
Zhu C, Stiehl T Sci Rep. 2024; 14(1):25060.
PMID: 39443599 PMC: 11500015. DOI: 10.1038/s41598-024-75429-7.
Boklund T, Snyder J, Gudmand-Hoeyer J, Larsen M, Knudsen T, Eickhardt-Dalboge C Front Immunol. 2024; 15:1384509.
PMID: 38846951 PMC: 11154009. DOI: 10.3389/fimmu.2024.1384509.
Lai X, Jiao X, Zhang H, Lei J NPJ Syst Biol Appl. 2024; 10(1):45.
PMID: 38678088 PMC: 11055880. DOI: 10.1038/s41540-024-00370-4.
Scherer M, Singh I, Braun M, Szu-Tu C, Kardorff M, Ruhle J bioRxiv. 2024; .
PMID: 38617287 PMC: 11014487. DOI: 10.1101/2024.04.01.587514.