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RNA-transfected autologous dendritic cell vaccine (Duke University)

Development stage
Unknown
Lead developer
Duke University
Modality
Dendritic Cell Vaccines → Immune Effector Cells → Other Cell Types → Cell Therapies, RNA Therapeutics → Nucleic Acid Therapeutics, Vaccines & Immunotherapeutics
Administration
Intranodal
01

Overview

This experimental autologous cellular immunotherapy, developed by Duke University, is designed for the treatment of metastatic melanoma. The vaccine is produced by harvesting a patient's own monocytes via leukapheresis and differentiating them into mature dendritic cells (DCs). These DCs are then transfected via electroporation with messenger RNA (mRNA) encoding tumor-associated melanoma antigens. In specific clinical protocols, a subset of these DCs is also transfected with mRNA encoding immune-modulatory proteins, such as GITR ligand (GITR-L) and a monoclonal antibody against CTLA-4. This approach aims to deliver immune modulators locally at the site of vaccination (typically the lymph nodes) to enhance the activation and expansion of tumor-specific T cells while avoiding the systemic toxicities associated with intravenous administration of checkpoint inhibitors. The vaccine is administered via ultrasound-guided intranodal injection.

Other names
Autologous RNA-transfected dendritic cell vaccineMelanoma DC vaccine (Duke)RNA-transfected mature autologous DC vaccine
02

Targets

CD4 (T lymphocyte surface antigen)CA9 (Carbonic anhydrase IX)CD8A (CD8 alpha/beta Coreceptor)

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