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C7R-EBVSTs is an investigational autologous cell therapy consisting of Epstein-Barr virus-specific T-cells (EBVSTs) genetically modified to express a chimeric antigen receptor (CAR) targeting CD70 and a constitutively active interleukin-7 receptor (C7R). The CAR component is derived from the extracellular domain of human CD27, the natural binding partner for CD70, which allows the engineered T-cells to recognize and eliminate CD70-expressing malignant cells. The inclusion of the C7R modification provides continuous IL-7 cytokine signaling, which is designed to enhance the persistence, expansion, and anti-tumor activity of the T-cells within the immunosuppressive tumor microenvironment. Developed by Baylor College of Medicine, this therapy is being evaluated in Phase 1 clinical trials (such as the CASEY and SEVENTY studies) for patients with relapsed or refractory hematologic malignancies, including acute myeloid leukemia (AML), B-cell leukemia, and T-cell leukemia.
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