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DAMP-Induced Allograft and Tumor Rejection: The Circle Is Closing
W G Land1,2,3, P Agostinis4, S Gasser5
1German Academy of Transplantation Medicine, Munich, Germany.
Summary
Damage-associated molecular patterns (DAMPs) released from dying cells can trigger organ transplant rejection. However, DAMPs also drive successful cancer immunotherapy, revealing a shared mechanism in inflammation and cell death.
Area of Science:
- Immunology
- Oncology
- Transplantation
Background:
- Damage-associated molecular patterns (DAMPs) are released from dying cells.
- DAMPs are implicated in allograft rejection following ischemia-reperfusion injury.
- DAMPs also play a crucial role in the success of cancer immunotherapy.
Purpose of the Study:
- To review the literature on the pathophysiological importance of DAMP release.
- To discuss the implications of DAMP release in allograft rejection and cancer immunotherapy.
- To highlight the mechanistic overlap between these two fields.
Main Methods:
- Literature review of recent studies on DAMPs.
- Analysis of DAMPs' role in cell death, inflammation, and immune responses.
- Comparative analysis of DAMPs' impact on transplantation and cancer immunotherapy.
Main Results:
- DAMP release is a key factor in allograft rejection.
- DAMPs act as potent triggers for anti-tumor immune responses.
- A significant mechanistic overlap exists between DAMPs in rejection and immunotherapy.
Conclusions:
- Regulated necrosis and inflammation provide a common mechanistic basis for allograft rejection and cancer immunotherapy.
- Understanding DAMPs' molecular characterization can benefit both transplant and oncology fields.
- Targeting DAMP-mediated pathways may offer novel therapeutic strategies.
Keywords:
basic (laboratory) research/sciencecancer/malignancy/neoplasiacell deathimmune regulationimmunobiologyorgan transplantation in generalrejectionrejection: antibody-mediated (ABMR)translational research/scienceMore Related Videos
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