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PSMA-CD16A CAR-T cells are an investigational adoptive cellular therapy designed for the treatment of prostate cancer. This specific chimeric antigen receptor (CAR) construct features a humanized J591-derived single-chain variable fragment (scFv) targeting Prostate-Specific Membrane Antigen (PSMA), fused to the transmembrane and intracellular signaling domains of CD16A (FcγRIIIa). Notably, the architecture omits canonical co-stimulatory domains such as 4-1BB or CD28, relying instead on the distinct signaling profile of the innate immune receptor CD16A. This design is intended to maintain robust antitumor cytotoxicity while attenuating the secretion of pro-inflammatory cytokines (TNF-α, IFN-γ, IL-2), potentially reducing the risk of cytokine release syndrome (CRS). Preclinical studies in LNCaP xenograft models have demonstrated antigen-dependent cytotoxicity, significant tumor regression, and improved overall survival compared to control groups.
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