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MAGE-3 peptide-pulsed autologous peripheral blood mononuclear cells + Melan-A peptide-pulsed autologous peripheral blood mononuclear cells

Development stage
Phase 2
Lead developer
National Cancer Institute
Modality
Cell Therapies, Vaccines & Immunotherapeutics
Administration
Intravenous, Intradermal
01

Overview

This therapeutic agent is an autologous cellular immunotherapy designed to treat malignancies expressing specific tumor-associated antigens, primarily metastatic melanoma. The process involves harvesting peripheral blood mononuclear cells (PBMCs) from a patient via leukapheresis. These cells are then pulsed ex vivo with synthetic peptides derived from the melanoma-associated antigen 3 (MAGE-3) and the melanoma antigen recognized by T-cells 1 (Melan-A, also known as MART-1). Upon re-infusion into the patient, the antigen-presenting cells (APCs) within the PBMC population present these epitopes to the endogenous immune system. This presentation is intended to prime and expand a population of cytotoxic T-lymphocytes (CTLs) that specifically recognize and eliminate tumor cells expressing MAGE-3 and Melan-A. This approach aims to bypass immune tolerance and generate a targeted, durable anti-tumor immune response.

Other names
MAGE-3 and Melan-A peptide-pulsed autologous peripheral blood mononuclear cellsMAGE3 and Melan-A peptide-pulsed autologous peripheral blood mononuclear cellsMAGE 3 and Melan-A peptide-pulsed autologous peripheral blood mononuclear cellsMAGE-3/Melan-A peptide-pulsed PBMC vaccineautologous MAGE-3/Melan-A peptide-pulsed PBMC vaccine
02

Targets

MART-1/HLA-A*02:01 (Melanoma-associated antigen (Melanoma antigen recognized by T cells 1, Melanocyte protein PMEL, Tyrosinase) peptide-HLA-A*02:01 complex)HLA-A*01 (Human leukocyte antigen A*01:01)

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