Allogeneic CAR T cell therapies for leukemia.
Waseem QasimPublished in: American journal of hematology (2019)
Allogeneic chimeric antigen receptor T (CAR T) cells can offer advantages over autologous T cell therapies, including the availability of "fit" cells for production, and elimination of risks associated with inadvertent transduction of leukemic blasts. However, allogeneic T cell therapies must address HLA barriers and conventionally rely on the availability of a suitable HLA-matched donor if graft-vs-host-disease and rejection effects are to be avoided. More recently, the incorporation of additional genome editing manipulations, to disrupt T cell receptor expression and address other critical pathways have been explored. Clinical trials are underway investigating non-HLA matched T cells expressing anti-CD19 CARs for the treatment of B cell acute lymphoblastic leukemia (B-ALL) and anti-CD123 CAR for acute myeloid leukemia (AML). Such approaches continue to be refined and improved to widen accessibility and reduce the cost of T cell therapies for a wider range of conditions.
Keyphrases
- acute myeloid leukemia
- bone marrow
- stem cell transplantation
- induced apoptosis
- genome editing
- acute lymphoblastic leukemia
- crispr cas
- allogeneic hematopoietic stem cell transplantation
- clinical trial
- cell cycle arrest
- hematopoietic stem cell
- high dose
- cell therapy
- endoplasmic reticulum stress
- stem cells
- cell death
- climate change
- oxidative stress
- low dose
- open label
- pi k akt
- study protocol