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cxcr2-transduced autologous tumor-infiltrating lymphocytes

Development stage
Phase 2
Lead developer
University of Texas MD Anderson Cancer Center
Modality
Cell Therapies, Gene Therapies
Administration
Intravenous
01

Overview

CXCR2-transduced autologous tumor-infiltrating lymphocytes (TILs) is an investigational adoptive cell therapy developed by MD Anderson Cancer Center for the treatment of metastatic melanoma. The therapy involves harvesting TILs from a patient's tumor, followed by genetic modification using a retroviral vector to express the chemokine receptor CXCR2 and a truncated nerve growth factor receptor (NGFR) as a selection marker. The rationale for this modification is that melanoma cells frequently secrete chemokines such as CXCL1 and CXCL8, but endogenous TILs often lack the corresponding receptor, CXCR2. By engineering TILs to express CXCR2, the therapy aims to enhance the trafficking and infiltration of these T cells into the tumor microenvironment. Following ex vivo expansion, the modified TILs are reinfused into the patient after a lymphodepleting chemotherapy regimen, typically in combination with high-dose interleukin-2 (IL-2) to promote T-cell survival and expansion in vivo.

Other names
CXCR2-transduced TILsCXCR-2-transduced TILsCXCR 2-transduced TILsCXCR2 and NGFR transduced autologous tumor-infiltrating lymphocytesCXCR-2 and NGFR transduced autologous tumor-infiltrating lymphocytesCXCR 2 and NGFR transduced autologous tumor-infiltrating lymphocytesCXCR2-transduced Autologous Tumor Infiltrating LymphocytesCXCR-2-transduced Autologous Tumor Infiltrating LymphocytesCXCR 2-transduced Autologous Tumor Infiltrating Lymphocytes
02

Targets

IL8 (C-X-C Motif Chemokine Ligand 8)pMHC-I (Peptide–MHC class I complex)CXCR2 (C-X-C Motif Chemokine Receptor 2)

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