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This is an investigational bispecific CAR-T cell therapy developed by the Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College. The therapy is designed to treat relapsed or refractory B-cell acute lymphoblastic leukemia (B-ALL) by engineering autologous T-cells to express a chimeric antigen receptor (CAR) that simultaneously targets both CD19 and CD22 antigens. The CAR construct utilizes scFvs derived from hybridoma clones HIB22 and HI19a, linked with a CD8α signal peptide and transmembrane domain, a 4-1BB costimulatory domain, and a CD3ζ cytoplasmic signaling region. This dual-targeting strategy is intended to overcome antigen escape and reduce relapse rates associated with single-target CD19 CAR-T therapies.
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