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multiepitope nucleic acid fusion vaccine

Development stage
Preclinical
Lead developer
Thomas Jefferson University
Modality
DNA Vaccines → Plasmid DNA → DNA Therapeutics → Nucleic Acid Therapeutics, Prophylactic Vaccines → Vaccines & Immunotherapeutics
Administration
Intramuscular
01

Overview

The multiepitope nucleic acid fusion vaccine is an experimental DNA plasmid-based immunotherapy designed for the prevention and treatment of metastatic uveal melanoma (UM). Developed by researchers at Thomas Jefferson University, the vaccine utilizes a plasmid backbone encoding a suite of immunogenic UM-associated epitopes, including the GNAQ/GNA11 Q209L driver mutation and antigens such as PMEL17, TYRP1, PRAME, and SLC45A2. To enhance T-cell activation and antigen presentation, the construct incorporates helper sequences like VP22, PADRE, and Tetanus toxoid P2, along with an MHC class I trafficking domain. Additionally, it features the CCL21 chemokine, transcriptionally linked via a P2A ribosomal skipping peptide, to serve as an intrinsic molecular adjuvant. Preclinical studies in transgenic mice have demonstrated the vaccine's ability to generate cytolytic T cells capable of recognizing and targeting UM cells.

Other names
T cell activating nucleic acid fusion vaccinemultiepitope vaccine
02

Targets

TYR (Tyrosinase)PMEL (Melanocyte Protein PMEL)PRAME (Preferentially expressed antigen in melanoma)GNAQ (G protein subunit alpha q)GNA11 (Guanine nucleotide-binding protein subunit alpha-11)MHC I (MHC class I})MC1R (Melanocortin Type 1 Receptor)TYRP1 (Tyrosinase-related protein 1)SLC45A2 (Membrane-associated transporter protein)CCL21 (Chemokine (C-C motif) ligand 21)

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