4.6 Review

Trial watch: dendritic cell vaccination for cancer immunotherapy

Journal

ONCOIMMUNOLOGY
Volume 8, Issue 11, Pages -

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/2162402X.2019.1638212

Keywords

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

Funding

  1. Research Foundation Flanders' (FWO) Excellence of Science (EOS) [30837538]
  2. KU Leuven via POR award funds [POR/16/040]
  3. FWO Postdoctoral Fellowship
  4. FWO fundamental research grants [G0584.12N, K202313N, GA01111N]
  5. KU Leuven [C24/18/064, C16/15/073]
  6. Kom Op Tegen Kanker (Stand up to Cancer)
  7. Flemish cancer society [2016/10728/2603]
  8. Olivia Fund [2017/LUF/00135]
  9. Ligue contre le Cancer (equipe labellisee)
  10. Agence National de la Recherche (ANR) - Projets blancs
  11. ANR
  12. ERA-Net for Research on Rare Diseases
  13. Association pour la recherche sur le cancer (ARC)
  14. Canceropole Ile-de-France
  15. Fondation pour la Recherche Medicale (FRM)
  16. Gustave Roussy Odyssea
  17. European Union
  18. Fondation Carrefour
  19. Highend Foreign Expert Program in China [GDW20171100085, GDW20181100051]
  20. Institut National du Cancer (INCa)
  21. Inserm (HTE)
  22. Institut Universitaire de France
  23. LeDucq Foundation
  24. LabEx Immuno-Oncology
  25. Seerave Foundation
  26. SIRIC Stratified Oncology Cell DNA Repair and Tumor Immune Elimination (SOCRATE)
  27. SIRIC Cancer Research and Personalized Medicine (CARPEM)
  28. US DoD
  29. Breast Cancer Research Program (BCRP) [BC180476P1]
  30. Dept. of Radiation Oncology at Weill Cornell Medicine (New York, US)
  31. Phosplatin (New York)
  32. Sotio a.s. (Prague, Czech Republic)
  33. Chancelerie des universites de Paris (Legs Poix)

Ask authors/readers for more resources

Dendritic- cells (DCs) have received considerable attention as potential targets for the development of anticancer vaccines. DC-based anticancer vaccination relies on patient-derived DCs pulsed with a source of tumor-associated antigens (TAAs) in the context of standardized maturation-cocktails, followed by their reinfusion. Extensive evidence has confirmed that DC-based vaccines can generate TAA-specific, cytotoxic T cells. Nonetheless, clinical efficacy of DC-based vaccines remains suboptimal, reflecting the widespread immunosuppression within tumors. Thus, clinical interest is being refocused on DC-based vaccines as combinatorial partners for T cell-targeting immunotherapies. Here, we summarize the most recent preclinical/clinical development of anticancer DC vaccination and discuss future perspectives for DC-based vaccines in immuno-oncology.

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