Clonal hematopoiesis (CH) in autologous transplant recipients and allogeneic transplant donors has genetic features and clinical associations that are distinct from each other and from non-cancer populations. CH in the setting of autologous transplant is enriched for mutations in DNA damage response pathway genes and is associated with adverse outcomes, including an increased risk of therapy-related myeloid neoplasm and inferior overall survival. Studies of CH in allogeneic transplant donors have yielded conflicting results but have generally shown evidence of potentiated alloimmunity in recipients, with some studies showing an association with favorable recipient outcomes.
Keyphrases
- bone marrow
- dna damage response
- stem cell transplantation
- hematopoietic stem cell
- room temperature
- kidney transplantation
- genome wide
- cell therapy
- case control
- papillary thyroid
- platelet rich plasma
- mesenchymal stem cells
- acute myeloid leukemia
- dna repair
- dendritic cells
- type diabetes
- stem cells
- gene expression
- dna methylation
- transcription factor
- ionic liquid
- skeletal muscle
- immune response
- squamous cell carcinoma
- lymph node metastasis
- free survival
- glycemic control
- genome wide identification
- insulin resistance
- childhood cancer