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Anti-CD84 CAR-T cells are chimeric antigen receptor T-cell therapies genetically engineered to recognize and kill cancer cells expressing the CD84 antigen. CD84, a member of the SLAM family (SLAMF5), is overexpressed on leukemic blasts in acute myeloid leukemia (AML) and T-cell acute lymphoblastic leukemia (T-ALL), with minimal expression on healthy hematopoietic stem progenitor cells (HSPC) and low presence in normal tissues. This therapy uses autologous or allogeneic T-cells modified with second-generation CAR constructs comprising anti-CD84 single-chain variable fragments (scFv) and 4-1BB co-stimulatory domains. Preclinical data show potent cytotoxicity against AML and T-ALL in vitro and in vivo, with low off-tumor toxicity to HSPC, supporting clinical trial development for relapsed/refractory AML and T-ALL as a potential bridge to transplant. The developer is Gyala Therapeutics, with ongoing clinical development in Spain[1][3][5].
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