4.6 Review

Trial watch: Dendritic cell-based anticancer immunotherapy

Journal

ONCOIMMUNOLOGY
Volume 6, Issue 7, Pages -

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/2162402X.2017.1328341

Keywords

Antigen cross-presentation; DAMPs; immune-checkpoint blockers; plasmacytoid dendritic cells; TLR signaling; tumor-infiltrating lymphocytes

Funding

  1. FWO-Vlaanderen, Belgium
  2. FWO [G060713N, G076617N]
  3. KU Leuven [C16/15/073]
  4. Belgian State [IAP7/32]
  5. Ligue contre le Cancer (equipe labelisee)
  6. Agence National de la Recherche (ANR)
  7. Association pour la recherche sur le cancer (ARC)
  8. Canceropole Ile-de-France
  9. AXA Chair for Longevity Research
  10. Institut National du Cancer (INCa)
  11. Fondation Bettencourt-Schueller
  12. Fondation de France
  13. Fondation pour la Recherche Medicale (FRM)
  14. European Commission (ArtForce)
  15. European Research Council (ERC)
  16. LabEx Immuno-Oncology
  17. SIRIC Stratified Oncology Cell DNA Repair and Tumor Immune Elimination (SOCRATE)
  18. SIRIC Cancer Research and Personalized Medicine (CARPEM)
  19. Paris Alliance of Cancer Research Institutes (PACRI)
  20. WCMC
  21. Sotio a.c. (Prague, Czech Republic)

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Dendritic cell (DC)-based vaccines against cancer have been extensively developed over the past two decades. Typically DC-based cancer immunotherapy entails loading patient-derived DCs with an appropriate source of tumor-associated antigens (TAAs) and efficient DC stimulation through a so-called maturation cocktail (typically a combination of pro-inflammatory cytokines and Toll-like receptor agonists), followed by DC reintroduction into patients. DC vaccines have been documented to (re) activate tumor-specific T cells in both preclinical and clinical settings. There is considerable clinical interest in combining DC-based anticancer vaccines with T cell-targeting immunotherapies. This reflects the established capacity of DC-based vaccines to generate a pool of TAA-specific effector T cells and facilitate their infiltration into the tumor bed. In this Trial Watch, we survey the latest trends in the preclinical and clinical development of DC-based anticancer therapeutics. We also highlight how the emergence of immune checkpoint blockers and adoptive T-cell transfer-based approaches has modified the clinical niche for DC-based vaccines within the wide cancer immunotherapy landscape.

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