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Autologous humanized anti-CD22 chimeric antigen receptor (CAR) T cells represent a cell-based gene therapy designed to treat B-cell malignancies. This therapy involves collecting T cells from a patient (autologous), genetically modifying them to express a CAR that specifically targets the CD22 protein found on the surface of malignant B cells, and then reinfusing these modified T cells back into the patient. The humanized component aims to reduce immunogenicity. Upon reinfusion, these CAR-T cells recognize and bind to CD22-expressing cancer cells, leading to their destruction. The therapy is being investigated for conditions such as refractory or relapsed B acute lymphoblastic leukemia (B-ALL).
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