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AAV9-CCL4 is an adeno-associated virus serotype 9 (AAV9) gene therapy vector designed to express the chemokine (C-C motif) ligand 4 (CCL4). Developed by researchers at the University of California, San Francisco (UCSF), it is administered via convection-enhanced delivery (CED) directly into the brain to treat glioblastoma. The therapeutic strategy involves using CCL4 to reprogram the immunosuppressive glioblastoma microenvironment by recruiting and activating anti-tumor immune cells, such as macrophages and CD8+ T cells. Preclinical studies have demonstrated that AAV9-CCL4 can suppress pro-tumor cytokines like IL-6 and LIF, potentially sensitizing "cold" tumors to immune checkpoint inhibition.
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