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Updated: Jan 2, 2026

18:48
In Vitro and In Vivo Assessment of T, B and Myeloid Cells Suppressive Activity and Humoral Responses from Transplant Recipients
Published on: August 12, 2017
14.8K
Clonal evolution and immune evasion in posttransplantation relapses.
Luca Vago1,2
1Unit of Immunogenetics, Leukemia Genomics and Immunobiology, and.
Hematology. American Society of Hematology. Education Program
|December 7, 2019
Summary
Disease relapse after allogeneic hematopoietic cell transplantation (allo-HCT) is common. Understanding evolutionary mechanisms like clonal selection and immune evasion is key to developing personalized therapies for hematological malignancies.
Area of Science:
- Hematology
- Immunology
- Evolutionary Biology
Background:
- Allogeneic hematopoietic cell transplantation (allo-HCT) has improved for hematological malignancies.
- Disease relapse remains a significant challenge with limited salvage options.
Observation:
- Relapses often result from evolutionary processes selecting for resistant disease variants.
- Changes in clonal structure and immunogenicity are observed at relapse.
Findings:
- Mechanisms include clonal evolution, immune checkpoint enforcement, and HLA alterations.
- Disease tropism for privileged sites can facilitate relapse.
- These mechanisms interact in complex patterns.
Implications:
- Understanding relapse mechanisms is crucial for personalized therapeutic strategies.
- Targeting evolutionary dynamics may improve allo-HCT outcomes.
- Further research into combined mechanisms can guide future treatments.
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