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tumor antigen-pulsed dendritic cell vaccine (NCI)

Development stage
Phase 2
Lead developer
National Cancer Institute
Modality
Dendritic Cell Vaccines → Immune Effector Cells → Other Cell Types → Cell Therapies, Vaccines & Immunotherapeutics
Administration
Intradermal, Subcutaneous
01

Overview

This personalized autologous dendritic cell vaccine was developed by the National Cancer Institute (NCI) for the treatment of pediatric solid tumors, specifically metastatic Ewing sarcoma and alveolar rhabdomyosarcoma. The therapy involves harvesting a patient's own dendritic cells and loading them ex vivo with synthetic peptides that represent the unique chromosomal translocation breakpoints characteristic of these tumors. For Ewing sarcoma, the vaccine typically targets the EWS-FLI1 or EWS-ERG fusion proteins, while for alveolar rhabdomyosarcoma, it targets PAX3-FOXO1 (PAX3-FKHR) or PAX7-FOXO1 (PAX7-FKHR). These pulsed dendritic cells are re-infused into the patient to act as professional antigen-presenting cells, priming and expanding tumor-specific cytotoxic T-lymphocytes. In clinical trial contexts, this vaccine has been evaluated following autologous T-cell transplantation and in combination with the protease inhibitor indinavir to enhance the anti-tumor immune response.

Other names
peptide-pulsed dendritic cell vaccineautologous dendritic cell vaccine (NCI)tumor antigen-pulsed dendritic cell vaccine-National Cancer Institute (NCI)-Ewing sarcoma-alveolar rhabdomyosarcoma
02

Targets

PAX7-FOXO1 (PAX7-FOXO1 fusion protein)PAX3-FOXO1 fusion protein-derived peptide-MHC complexEWS-ERG-MHC (Ewing sarcoma breakpoint region 1-ETS transcription factor ERG fusion protein-derived peptides presented on Major Histocompatibility Complex)Ewing sarcoma breakpoint region 1-Friend leukemia integration 1 transcription factor fusion protein-derived peptides presented on Major Histocompatibility Complex

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