Department of Regenerative Medicine Research, Texas Heart Institute, Houston, TX.
Division of Cardiothoracic Transplantation and Mechanical Circulatory Support, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, TX.
Transplantation. 2023 Aug 1;107(8):1687-1697. doi: 10.1097/TP.0000000000004503. Epub 2023 Jul 20.
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.
肺移植受者的存活率比其他所有实体器官移植受者都要差,这主要是因为原发性移植物功能障碍(PGD),这是一种主要的急性肺损伤形式,影响了三分之一的肺移植受者在移植后 72 小时内。PGD 是缺血再灌注损伤的临床表现,也是导致早期发病率和死亡率的主要原因。尽管 PGD 对肺移植结果有影响,但目前尚无靶向治疗方法;因此,治疗仍然是支持性的,而且效果不大。本综述重点介绍了导致 PGD 的缺血再灌注损伤的分子和先天免疫机制。我们还讨论了旨在发现更好地预测 PGD 的生物标志物和可能改善肺移植结果的潜在靶向干预措施的新研究。