Drug intelligence / Profile preview

IL-21-primed autologous CD8-positive T-lymphocytes

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

Overview

IL-21-primed autologous CD8-positive T-lymphocyte therapy is an investigational adoptive cell therapy developed by the M.D. Anderson Cancer Center for the treatment of recurrent or platinum-resistant ovarian cancer. The therapeutic process involves the isolation of a patient's own CD8+ T cells, which are then primed ex vivo with Interleukin-21 (IL-21) to induce a central memory phenotype and enhance their cytotoxic potential against ovarian cancer antigens. Once re-infused, these tumor-antigen-specific cytotoxic T lymphocytes (CTLs) are intended to recognize and eliminate malignant cells. In clinical trial settings (such as NCT03318900), this cell therapy is administered following lymphodepleting chemotherapy and in combination with aldesleukin (IL-2) to support T-cell expansion and utomilumab (a 4-1BB agonist) to provide necessary costimulatory signals and improve T-cell persistence.

Other names
CD8-positive T-lymphocyte-M.D. Anderson Cancer Center-ovarian cancerCD-8-positive T-lymphocyte-M.D. Anderson Cancer Center-ovarian cancerCD 8-positive T-lymphocyte-M.D. Anderson Cancer Center-ovarian cancerIL-21-primed CD8+ tumor antigen-specific T cellsAdoptive T-cell TherapyCD8-Positive T-LymphocyteCD-8-Positive T-LymphocyteCD 8-Positive T-Lymphocyte
02

Targets

New York esophageal squamous cell carcinoma 1 peptide–Human leukocyte antigen class I complex (NY-ESO-1–HLA-I complex)

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