Antigenic Targets for the Immunotherapy of Acute Myeloid Leukaemia.
Ghazala Naz KhanKim OrchardBarbara-Ann GuinnPublished in: Journal of clinical medicine (2019)
One of the most promising approaches to preventing relapse is the stimulation of the body's own immune system to kill residual cancer cells after conventional therapy has destroyed the bulk of the tumour. In acute myeloid leukaemia (AML), the high frequency with which patients achieve first remission, and the diffuse nature of the disease throughout the periphery, makes immunotherapy particularly appealing following induction and consolidation therapy, using chemotherapy, and where possible stem cell transplantation. Immunotherapy could be used to remove residual disease, including leukaemic stem cells from the farthest recesses of the body, reducing, if not eliminating, the prospect of relapse. The identification of novel antigens that exist at disease presentation and can act as targets for immunotherapy have also proved useful in helping us to gain a better understand of the biology that belies AML. It appears that there is an additional function of leukaemia associated antigens as biomarkers of disease state and survival. Here, we discuss these findings.
Keyphrases
- high frequency
- stem cell transplantation
- acute myeloid leukemia
- dendritic cells
- liver failure
- end stage renal disease
- transcranial magnetic stimulation
- respiratory failure
- high dose
- free survival
- bone marrow
- newly diagnosed
- chronic kidney disease
- stem cells
- peritoneal dialysis
- immune response
- hepatitis b virus
- allogeneic hematopoietic stem cell transplantation
- intensive care unit
- patient reported outcomes
- extracorporeal membrane oxygenation
- patient reported