Primary Graft Dysfunction in Lung Transplantation: A Review of Mechanisms and Future Applications

Author:

Chacon-Alberty Lourdes1,Fernandez Ramiro2,Jindra Peter2,King Madelyn1,Rosas Ivan3,Hochman-Mendez Camila1,Loor Gabriel24

Affiliation:

1. Department of Regenerative Medicine Research, Texas Heart Institute, Houston, TX.

2. Division of Cardiothoracic Transplantation and Mechanical Circulatory Support, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, TX.

3. Department of Medicine, Baylor College of Medicine, Houston, TX.

4. Cardiothoracic Surgery Professional Staff, The Texas Heart Institute, Houston, TX.

Abstract

Lung allograft recipients have worse survival than all other solid organ transplant recipients, largely because of primary graft dysfunction (PGD), a major form of acute lung injury affecting a third of lung recipients within the first 72 h after transplant. PGD is the clinical manifestation of ischemia–reperfusion injury and represents the predominate cause of early morbidity and mortality. Despite PGD’s impact on lung transplant outcomes, no targeted therapies are currently available; hence, care remains supportive and largely ineffective. This review focuses on molecular and innate immune mechanisms of ischemia–reperfusion injury leading to PGD. We also discuss novel research aimed at discovering biomarkers that could better predict PGD and potential targeted interventions that may improve outcomes in lung transplantation.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Transplantation

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