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Autologous anti-CD83 CAR T-cells are an investigational genetically engineered cell therapy designed to treat relapsed or refractory acute myeloid leukemia (AML). The therapy involves harvesting a patient's own T cells and modifying them to express a chimeric antigen receptor (CAR) that targets CD83, a protein expressed on AML blasts (abnormal immature white blood cells). Beyond its role as a tumor-associated antigen in AML, CD83 is also expressed on mature dendritic cells that mediate graft-versus-host disease (GVHD). By targeting CD83, this therapy aims to achieve dual therapeutic goals: the direct cytotoxic elimination of leukemia cells and the potential prevention or mitigation of GVHD and myeloid aplasia, which are common complications in patients undergoing hematopoietic stem cell transplantation.
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