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
- dna repair
- mesenchymal stem cells
- dendritic cells
- acute myeloid leukemia
- high dose
- low grade
- type diabetes
- stem cells
- squamous cell
- adipose tissue
- skeletal muscle
- dna methylation
- gene expression
- metabolic syndrome
- immune response
- ionic liquid
- squamous cell carcinoma
- young adults
- bioinformatics analysis
- glycemic control