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iPS-T cell therapy is a form of cell therapy in which **T cells are generated from human induced pluripotent stem cells (iPSCs)**, often for adoptive immunotherapy, including cancer and autoimmune indications. iPSCs can be differentiated into T cells with defined antigen specificity through genetic engineering, such as introducing specific T cell receptors (TCRs) or chimeric antigen receptors (CARs). This approach enables the production of *off-the-shelf* T cell products with unlimited scalability and potential for standardization, hypo-immunogenicity, and rigorous safety testing. iPSC-derived T cells can have enhanced proliferative capacity and memory-like features, extending their anti-tumor efficacy relative to conventional effector T cells. The therapy addresses limitations of autologous T cell manufacturing, such as donor variability and supply constraints, by providing a consistent, renewable cell source suitable for large-scale GMP manufacturing[2][4][7][9][14]. Main mechanisms involve immune targeting of disease—typically cancer—using engineered antigen recognition. This therapy is in experimental and early clinical phases and is being developed for oncological and autoimmune diseases.
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