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This is an investigational autologous chimeric antigen receptor T (CAR-T) cell therapy developed by Sun Yat-sen University for the treatment of advanced non-small cell lung cancer (NSCLC). The patient's own T cells are genetically modified using a lentiviral vector to express a CAR comprising a PD-L1-specific single-chain variable fragment (scFv) derived from a monoclonal antibody, linked to intracellular signaling domains including CD3 zeta and costimulatory molecules CD137 (4-1BB) and CD28. This modification allows the T cells to specifically recognize and eliminate tumor cells expressing Programmed death-ligand 1 (PD-L1). The therapy is currently being evaluated in Phase I clinical trials focusing on safety, toxicity, and preliminary efficacy in NSCLC patients who have failed standard treatments and show positive PD-L1 expression.
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