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DAMP-Induced Allograft and Tumor Rejection: The Circle Is Closing

期刊

AMERICAN JOURNAL OF TRANSPLANTATION
卷 16, 期 12, 页码 3322-3337

出版社

WILEY
DOI: 10.1111/ajt.14012

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资金

  1. German Research Foundation (Cluster of Excellence) [EXC306]
  2. FWO-Vlaanderen
  3. National Research Agency's (Agence Nationale de Recherche
  4. ANR)
  5. Investment for the Future Program's (Programme des Investissements d'Avenir
  6. PIA) Laboratoire d'Excellence (LabEx) TRANSPLANTEX [ANR-11-LABX-0070_TRANSPLANTEX]
  7. INSERM [UMR_S 1109]
  8. ANR
  9. Franco-Japanese NextGen HLA laboratory
  10. Ligue contre le Cancer (equipe labelisee)
  11. Agence National de la Recherche (ANR)-Projets blancs
  12. ANR under the frame of E-Rare-2
  13. ERA-Net for Research on Rare Diseases
  14. Association pour la recherche sur le cancer (ARC)
  15. Canceropole Ile-de-France
  16. Institut National du Cancer (INCa)
  17. Institut Universitaire de France
  18. Fondation pour la Recherche Medicale (FRM)
  19. European Commission (ArtForce)
  20. European Research Council (ERC)
  21. LeDucq Foundation
  22. LabEx Immuno-Oncology
  23. SIRIC Stratified Oncology Cell DNA Repair and Tumor Immune Elimination (SOCRATE)
  24. SIRIC Cancer Research and Personalized Medicine (CARPEM)
  25. Paris Alliance of Cancer Research Institutes (PACRI)

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The pathophysiological importance of the immunogenicity of damage-associated molecular patterns (DAMPs) has been pinpointed by their identification as triggers of allograft rejection following release from dying cells, such as after ischemia-reperfusion injury. In cancers, however, this strong trigger of a specific immune response gives rise to the success of cancer immunotherapy. Here, we review the recently literature on the pathophysiological importance of DAMP release and discuss the implications of these processes for allograft rejection and cancer immunotherapy, revealing a striking mechanistic overlap. We conclude that these two fields share a common mechanistic basis of regulated necrosis and inflammation, the molecular characterization of which may be helpful for both oncologists and the transplant community.

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