Key result
Fibrin deposition and fibrinolysis regulate organ damage and recovery after solid organ transplantation.
This review highlights the dual role of fibrin deposition in organ transplantation, suggesting that while early fibrin may be protective, persistent deposition and dysfunctional fibrinolysis can propagate tissue damage and worsen outcomes.
Organ transplantation represents a unique environment in which the donor organ undergoes a systemic insult worsened by procurement that is followed by ischemia-reperfusion injury on revascularization. Historically, microvascular thrombosis during sequential injury was considered a cause of organ dysfunction. However, recent data challenge the concept that fibrin deposition in organs drives pathology and instead suggest that the hemostatic system may play an important role in organ recovery. Although fibrin may be protective in the early setting of organ injury, persistent fibrin deposition augments inflammatory leukocyte recruitment that propagates tissue damage. Because the timing of fibrin deposition within the transplanted organ influences both damage and repair, the fibrinolytic system plays an essential role in organ recovery after transplantation. Dysfunctional fibrinolysis is linked to adverse outcomes in many diseases but has received less attention in organ transplantation. This review covers the physiological and pathological role of fibrin formation in liver, kidney, and lung transplantation and discusses how activation of the fibrinolytic system may ultimately modulate outcome.
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Moore et al. (2025) conducted a review in Liver, kidney, and lung transplantation. Fibrin formation and fibrinolysis was evaluated. Fibrin deposition and the fibrinolytic system play essential roles in organ recovery and damage after liver, kidney, and lung transplantation.
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