Target intelligence / Profile preview

Autologous dendritic cell-multiple myeloma fusion vaccine (DC/MM fusion vaccine)

Target
DC/MM fusion vaccine
Molecular classification
Cell-based therapy, Cancer vaccine, Immunotherapy
01

Overview

The autologous dendritic cell-multiple myeloma (DC/MM) fusion vaccine is a personalized cellular immunotherapy designed to treat multiple myeloma (Avigan et al., 2004, Clinical Cancer Research). It is created by fusing a patient's own dendritic cells, which are professional antigen-presenting cells, with their own malignant plasma cells using polyethylene glycol (Rosenblatt et al., 2011, Blood). This fusion process results in a hybrid cell that displays a comprehensive array of tumor-associated antigens in the context of essential co-stimulatory molecules like MHC class I and II, CD80, and CD86 (Vasir et al., 2005, British Journal of Haematology). When administered back to the patient, typically alongside GM-CSF to enhance recruitment, the vaccine stimulates the expansion of tumor-reactive CD4+ and CD8+ T cells (NIH, ClinicalTrials.gov, NCT02728102). These T cells are then capable of identifying and destroying residual myeloma cells throughout the body. This approach is particularly focused on achieving long-term remission by targeting minimal residual disease following standard treatments like autologous stem cell transplantation.

Other names
DC-myeloma fusionDendritic cell-tumor cell fusionAutologous DC/MM fusion productDC/MM fusion
02

Mechanism of action

Induction of a broad, polyclonal T-cell response against multiple myeloma by presenting a comprehensive array of patient-specific tumor-associated antigens within the context of dendritic cell-derived co-stimulatory signals.

03

Biological functions

Antigen presentationT-cell activationImmune response inductionPolyclonal T-cell expansion
04

Disease associations

Multiple myeloma
05

Safety considerations

Injection site reactionsFlu-like symptomsManufacturing complexity and feasibilityRequirement for sufficient autologous tumor and dendritic cell collection
06

Interacting drugs

Granulocyte-macrophage colony-stimulating factor (GM-CSF)

3 more in the full profile.

07

Biomarkers

Interferon-gamma (IFN-gamma) productionM-protein levelsMinimal residual disease (MRD) statusTumor-reactive T-cell frequency

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