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与延长冷保存用于移植相比,常温离体灌注可预防肺损伤。

Normothermic ex vivo perfusion prevents lung injury compared to extended cold preservation for transplantation.

作者信息

Cypel M, Rubacha M, Yeung J, Hirayama S, Torbicki K, Madonik M, Fischer S, Hwang D, Pierre A, Waddell T K, de Perrot M, Liu M, Keshavjee S

机构信息

Toronto Lung Transplant Program, Division of Thoracic Surgery, Latner Thoracic Laboratories, University of Toronto, Toronto, ON, Canada.

出版信息

Am J Transplant. 2009 Oct;9(10):2262-9. doi: 10.1111/j.1600-6143.2009.02775.x. Epub 2009 Aug 6.


DOI:10.1111/j.1600-6143.2009.02775.x
PMID:19663886
Abstract

Treatment of injured donor lungs ex vivo to accelerate organ recovery and ameliorate reperfusion injury could have a major impact in lung transplantation. We have recently demonstrated a feasible technique for prolonged (12 h) normothermic ex vivo lung perfusion (EVLP). This study was performed to examine the impact of prolonged EVLP on ischemic injury. Pig donor lungs were cold preserved in Perfadex for 12 h and subsequently divided into two groups: cold static preservation (CSP) or EVLP at 37 degrees C with Steen solution for a further 12 h (total 24 h preservation). Lungs were then transplanted and reperfused for 4 h. EVLP preservation resulted in significantly better lung oxygenation (PaO(2) 531 +/- 43 vs. 244 +/- 49 mmHg, p < 0.01) and lower edema formation rates after transplantation. Alveolar epithelial cell tight junction integrity, evaluated by zona occludens-1 protein staining, was disrupted in the cell membranes after prolonged CSP but not after EVLP. The maintenance of integrity of barrier function during EVLP translates into significant attenuation of reperfusion injury and improved graft performance after transplantation. Integrity of functional metabolic pathways during normothermic perfusion was confirmed by effective gene transfer and GFP protein synthesis by lung alveolar cells. In conclusion, EVLP prevents ongoing injury associated with prolonged ischemia and accelerates lung recovery.

摘要

对受损供体肺进行体外处理以加速器官恢复并减轻再灌注损伤,可能会对肺移植产生重大影响。我们最近展示了一种可行的技术,用于延长(12小时)常温体外肺灌注(EVLP)。本研究旨在探讨延长EVLP对缺血性损伤的影响。猪供体肺在Perfadex中冷保存12小时,随后分为两组:冷静态保存(CSP)或在37℃下用Steen溶液进行EVLP再灌注12小时(总共保存24小时)。然后进行肺移植并再灌注4小时。EVLP保存导致肺氧合显著改善(PaO₂ 531±43 vs. 244±49 mmHg,p<0.01),移植后水肿形成率降低。通过闭合蛋白-1蛋白染色评估,延长CSP后肺泡上皮细胞紧密连接完整性在细胞膜中被破坏,但EVLP后未被破坏。EVLP期间屏障功能完整性的维持转化为再灌注损伤的显著减轻和移植后移植物性能的改善。通过肺肺泡细胞有效的基因转移和GFP蛋白合成证实了常温灌注期间功能代谢途径的完整性。总之,EVLP可预防与长时间缺血相关的持续损伤并加速肺恢复。

相似文献

[1]
Normothermic ex vivo perfusion prevents lung injury compared to extended cold preservation for transplantation.

Am J Transplant. 2009-10

[2]
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J Heart Lung Transplant. 2015-6-10

[3]
Technique for prolonged normothermic ex vivo lung perfusion.

J Heart Lung Transplant. 2008-12

[4]
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Int J Artif Organs. 2019-7

[5]
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J Thorac Cardiovasc Surg. 2017-4-12

[6]
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J Thorac Cardiovasc Surg. 2012-8-31

[7]
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Transpl Int. 2018-7-31

[8]
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Transplantation. 2015-12

[9]
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J Heart Lung Transplant. 2012-2

[10]
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J Heart Lung Transplant. 2017-2-20

引用本文的文献

[1]
Application of artificial intelligence and machine learning in lung transplantation: a comprehensive review.

Front Digit Health. 2025-5-1

[2]
A novel modified Steen solution limits inflammatory processes during ex vivo lung perfusion and improves graft function post-transplantation.

JHLT Open. 2024-4-2

[3]
Activation of Nrf2 pathway by 4-Octyl itaconate enhances donor lung function in cold preservation settings.

Respir Res. 2025-2-27

[4]
Hepatic conditioning results in better lung endothelial cell preservation under hypoxic environment in vitro.

Int J Artif Organs. 2025-2

[5]
Donor Lungs' Procurement Implementation with Ex Vivo Lung Perfusion in a Low-Volume Lung Transplant Center.

Life (Basel). 2024-12-31

[6]
Ex vivo MFG-E8 treatment improves the function of lungs procured from cardiac death donors in preclinical porcine model.

Heliyon. 2024-6-25

[7]
The role of lung-restricted autoantibodies in the development of primary and chronic graft dysfunction.

Front Transplant. 2023-11-9

[8]
Porcine lungs perfused with three different flows using the 8-h open-atrium cellular lung perfusion technique.

Front Bioeng Biotechnol. 2024-6-25

[9]
Proteome of Personalized Tissue-Engineered Veins.

ACS Omega. 2024-3-19

[10]
Male versus female inflammatory response after brain death model followed by ex vivo lung perfusion.

Biol Sex Differ. 2024-1-29

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