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Autologous interleukin-12-expressing acute myeloid leukemia cells is an investigational cell and gene therapy designed for acute myeloid leukemia (AML). This therapy involves genetically engineering a patient's own (autologous) AML cells to express and secrete Interleukin-12 (IL-12) using a lentiviral vector. When re-infused, these modified cells act as an in situ vaccine, stimulating a potent anti-tumor immune response. The secreted IL-12 activates the patient's immune system, leading to the recognition and elimination of leukemia cells, including those not expressing IL-12. This approach aims to induce long-term immunological memory against AML and has shown preclinical promise in inhibiting angiogenesis and inducing apoptosis in AML cells. It is currently in Phase I clinical trials for patients with relapsed or high-risk AML.
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