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The autologous RNA-electroporated mature dendritic cell vaccine is an investigational, patient-specific cellular immunotherapy developed by Radboud University Nijmegen Medical Centre for the treatment of multiple myeloma. The manufacturing process involves isolating monocytes from the patient via apheresis, differentiating them into mature dendritic cells (DCs), and subsequently electroporating the DCs with mRNA encoding three tumor-associated antigens (TAAs): MAGE-3, Survivin, and B-cell maturation antigen (BCMA). Keyhole limpet hemocyanin (KLH) is added as an immunological adjuvant and tracer. The vaccine is designed to stimulate a T-cell mediated immune response against myeloma cells expressing these TAAs. In clinical evaluation, it has been administered to patients in minimal residual disease (MRD) following autologous stem cell transplantation to assess safety and immunogenicity.
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