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CD8αH&TM-41BBζ CAR-T cells are an experimental chimeric antigen receptor (CAR) T-cell therapy designed to target CD70, a protein frequently expressed in acute myeloid leukemia (AML) and other malignancies. This specific construct utilizes the natural ligand CD27 as the antigen-binding domain, fused to a CD8α hinge and transmembrane domain, a 4-1BB (CD137) costimulatory domain, and a CD3ζ signaling endodomain. Developed by researchers at the University of Lausanne and CHUV, this CAR-T variant was evaluated alongside other CD27-based designs to optimize anti-leukemic potency and circumvent the natural cleavage of CD27. In preclinical studies, while this construct showed activity, it was compared against a redesigned CD8αH-CD27ζ CAR which demonstrated superior efficacy in sequential killing assays and in vivo mouse models.
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