Drug intelligence / Profile preview

autologous T-antigen-presenting cells

Development stage
Phase 1
Lead developer
Fred Hutchinson Cancer Center
Modality
Cell Therapies, Vaccines & Immunotherapeutics
Administration
Intravenous
01

Overview

Autologous T-antigen-presenting cells (T-APC) is an experimental cell-based immunotherapy developed by the Fred Hutchinson Cancer Center for the treatment of metastatic melanoma. This approach involves the use of a patient's own T cells that have been modified to function as antigen-presenting cells. In clinical protocols, these T-APCs are typically administered as a vaccine following the adoptive transfer of therapeutic autologous CD8+ antigen-specific T-cell clones (CTLs). The T-APCs are designed to present melanoma-associated antigens directly to the transferred CTLs *in vivo*, providing the necessary costimulatory signals to promote the expansion, survival, and long-term persistence of the anti-tumor T cells. This regimen is often combined with lymphodepleting chemotherapy (such as cyclophosphamide) and systemic cytokine support (such as aldesleukin) to optimize the immune environment for tumor eradication.

Other names
autologous T-antigen-presenting cells vaccineT-APC vaccineautologous T-APC
02

Targets

MAGE-A3 TCR (T cell receptor / peptide–MHC complex derived from MAGE-A3/A6)CD28 (Cluster of Differentiation 28)LFA-1 (Integrin αLβ2)

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