Sterile Pancreas Inflammation during Preservation and after Transplantation.
Delphine KervellaBenoît MesnardThomas PrudhommeSarah BruneauChristophe MassetDiego CantarovichGilles BlanchoJulien BranchereauPublished in: International journal of molecular sciences (2023)
The pancreas is very susceptible to ischemia-reperfusion injury. Early graft losses due to pancreatitis and thrombosis represent a major issue after pancreas transplantation. Sterile inflammation during organ procurement (during brain death and ischemia-reperfusion) and after transplantation affects organ outcomes. Sterile inflammation of the pancreas linked to ischemia-reperfusion injury involves the activation of innate immune cell subsets such as macrophages and neutrophils, following tissue damage and release of damage-associated molecular patterns and pro-inflammatory cytokines. Macrophages and neutrophils favor tissue invasion by other immune cells, have deleterious effects or functions, and promote tissue fibrosis. However, some innate cell subsets may promote tissue repair. This outburst of sterile inflammation promotes adaptive immunity activation via antigen exposure and activation of antigen-presenting cells. Better controlling sterile inflammation during pancreas preservation and after transplantation is of utmost interest in order to decrease early allograft loss (in particular thrombosis) and increase long-term allograft survival. In this regard, perfusion techniques that are currently being implemented represent a promising tool to decrease global inflammation and modulate the immune response.
Keyphrases
- oxidative stress
- immune response
- ischemia reperfusion injury
- induced apoptosis
- cell therapy
- pulmonary embolism
- magnetic resonance imaging
- adipose tissue
- computed tomography
- stem cells
- insulin resistance
- metabolic syndrome
- single cell
- magnetic resonance
- cell cycle arrest
- kidney transplantation
- brain injury
- inflammatory response
- cell migration
- resting state
- single molecule
- anti inflammatory