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Autologous human-derived anti-CD19 CAR-T cells (specifically developed under the code YK-hCD19BB-002) represent an investigational chimeric antigen receptor (CAR) T-cell therapy designed to target CD19-positive B-cell malignancies, including relapsed or refractory acute lymphoblastic leukemia (r/r B-ALL). Unlike conventional CAR-T therapies that utilize murine-derived single-chain variable fragments (scFvs) which can trigger immunogenic clearance and limit persistence, this therapy employs a fully human or human-derived scFv. The CAR construct typically incorporates a 4-1BB costimulatory domain and a CD3ζ signaling domain. By utilizing patient-derived T cells engineered to express this humanized CAR, the therapy aims to minimize immunogenicity, enhance in vivo persistence, and improve clinical outcomes in patients who have relapsed after or are resistant to prior murine-derived CD19 CAR-T therapies.
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