Your browser doesn't support javascript.
loading
Clonal hematopoiesis of indeterminate potential and its impact on patient trajectories after stem cell transplantation.
Park, Derek S; Akuffo, Afua A; Muench, David E; Grimes, H Leighton; Epling-Burnette, Pearlie K; Maini, Philip K; Anderson, Alexander R A; Bonsall, Michael B.
Afiliação
  • Park DS; Mathematical Ecology Research Group, Department of Zoology, University of Oxford, Oxford, United Kingdom.
  • Akuffo AA; Department of Integrated Mathematical Oncology, H. Lee Moffitt Cancer Center, Tampa, Florida, USA.
  • Muench DE; Department of Immunology, H. Lee Moffitt Cancer Center, Tampa, Florida, USA.
  • Grimes HL; Division of Immunobiology and Center for Systems Immunology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
  • Epling-Burnette PK; Division of Immunobiology and Center for Systems Immunology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
  • Maini PK; Department of Immunology, H. Lee Moffitt Cancer Center, Tampa, Florida, USA.
  • Anderson ARA; Wolfson Centre for Mathematical Biology, Mathematical Institute, University of Oxford, Oxford, United Kingdom.
  • Bonsall MB; Department of Integrated Mathematical Oncology, H. Lee Moffitt Cancer Center, Tampa, Florida, USA.
PLoS Comput Biol ; 15(4): e1006913, 2019 04.
Article em En | MEDLINE | ID: mdl-31026273
ABSTRACT
Clonal hematopoiesis of indeterminate potential (CHIP) is a recently identified process where older patients accumulate distinct subclones defined by recurring somatic mutations in hematopoietic stem cells. CHIP's implications for stem cell transplantation have been harder to identify due to the high degree of mutational heterogeneity that is present within the genetically distinct subclones. In order to gain a better understanding of CHIP and the impact of clonal dynamics on transplantation outcomes, we created a mathematical model of clonal competition dynamics. Our analyses highlight the importance of understanding competition intensity between healthy and mutant clones. Importantly, we highlight the risk that CHIP poses in leading to dominance of precancerous mutant clones and the risk of donor derived leukemia. Furthermore, we estimate the degree of competition intensity and bone marrow niche decline in mice during aging by using our modeling framework. Together, our work highlights the importance of better characterizing the ecological and clonal composition in hematopoietic donor populations at the time of stem cell transplantation.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Células-Tronco Hematopoéticas / Transplante de Células-Tronco / Hematopoese / Modelos Biológicos Limite: Animals / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Células-Tronco Hematopoéticas / Transplante de Células-Tronco / Hematopoese / Modelos Biológicos Limite: Animals / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article