AI Article Synopsis

  • Allogeneic hematopoietic stem cell transplantation (allo-HSCT) shows promise as a cure for myelodysplastic neoplasms (MDSs) and other blood cancers.
  • A study of 21 MDS patients post-transplantation revealed 38% developed new genetic mutations, indicating clonal hematopoiesis (CH) from donor cells and a higher incidence of CH compared to healthy individuals.
  • Additionally, telomere length in these patients shortened significantly, suggesting stress and rapid cell division in the new bone marrow environment may accelerate genetic changes.

Article Abstract

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a potential cure for myelodysplastic neoplasms (MDSs) and other hematologic malignancies. This study investigates post-transplantation genetic evolution and telomere dynamics in hematopoietic cells, with a focus on clonal hematopoiesis (CH). We conducted a longitudinal analysis of 21 MDS patients who underwent allo-HSCT between September 2009 and February 2015. Genetic profiles of hematopoietic cells from both recipients and donors were compared at equivalent pre- and post-transplantation time points. Targeted sequencing identified CH-associated mutations, and real-time quantitative PCR measured telomere length. Furthermore, we compared CH incidence between recipients and age-matched controls from the GENIE cohort from routine health checkups. Post-allo-HSCT, 38% of recipients developed somatic mutations not detected before transplantation, indicating de novo CH originating from donor cells. Compared to age-matched healthy controls, recipients showed a significantly higher incidence of CH, suggesting increased susceptibility to genetic changes post-transplant. Telomere length analysis also revealed accelerated shortening in transplanted cells, highlighting the heightened stress and proliferation demands in the new microenvironment. Our findings reveal a notable incidence of donor-derived CH in allo-HSCT recipients, alongside significant telomere attrition. This suggests the potential influence of the marrow microenvironment on genetic and molecular changes in hematopoietic cells.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11477089PMC
http://dx.doi.org/10.3390/ijms251910258DOI Listing

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