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mage3 peptide-pulsed dendritic cell-derived exosomes

Development stage
Unknown
Lead developer
Anosys
Modality
Dendritic Cell Vaccines → Immune Effector Cells → Other Cell Types → Cell Therapies, Lipid-based Nanoparticles → Nanoparticles → Drug Delivery Systems, Vaccines & Immunotherapeutics
Administration
Intradermal, Subcutaneous
01

Overview

MAGE3 peptide-pulsed dendritic cell-derived exosomes (Dex) is an experimental autologous cancer vaccine and biologic. It consists of nanomeric vesicles (50–90 nm) purified from a patient's own monocyte-derived dendritic cell (DC) cultures, which are then loaded with MAGE3 tumor-associated peptide antigens (including MHC class I and MHC class II epitopes). These exosomes carry functional MHC/peptide complexes that are transferred to endogenous dendritic cells to prime MAGE3-specific CD4+ and CD8+ T cell immune responses. Additionally, the therapy promotes NK cell activation via NKG2D and IL-15Rα pathways. Developed by Institut Curie and Anosys, this immunotherapy has been investigated in Phase I clinical trials for the treatment of MAGE3-expressing metastatic melanoma and non-small cell lung cancer (NSCLC).

Other names
MAGE3-pulsed DexMAGE-3-pulsed DexMAGE 3-pulsed DexMAGE3-pulsed dendritic cell-derived exosomesMAGE-3-pulsed dendritic cell-derived exosomesMAGE 3-pulsed dendritic cell-derived exosomesautologous dendritic cell-derived exosomes pulsed with MAGE3 peptides
02

Targets

CD2 (T-cell Surface Antigen CD2)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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