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肺移植中的气道上皮:移植后并发症的潜在因素?

Airway epithelium in lung transplantation: a potential actor for post-transplant complications?

机构信息

Aix-Marseille University, APHM, Department of Respiratory Medicine and Lung Transplantation, Marseille, France.

Aix-Marseille University, INSERM, INRAE, C2VN, Marseille, France.

出版信息

Eur Respir Rev. 2024 Nov 27;33(174). doi: 10.1183/16000617.0093-2024. Print 2024 Oct.

DOI:10.1183/16000617.0093-2024
PMID:39603662
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11600126/
Abstract

Lung transplantation, a critical intervention for end-stage lung diseases, is frequently challenged by post-transplant complications. Indeed, primary graft dysfunction, anastomotic complications, infections and acute and chronic rejections pose significant hurdles in lung transplantation. While evidence regarding the role of airway epithelium after lung transplantation is still emerging, its importance is becoming increasingly recognised. This review looks at the complex involvement of airway epithelium in various post-transplant complications, while emphasising the utility of airway epithelial culture as a research model. In summary, by elucidating the involvement of airway epithelium in each post-transplant complication and explaining these intricate processes, the review aims to guide specific future research efforts and therapeutic strategies aimed at improving lung transplant outcomes and enhancing patient care.

摘要

肺移植是治疗终末期肺部疾病的关键手段,但经常受到移植后并发症的挑战。实际上,原发性移植物功能障碍、吻合口并发症、感染以及急性和慢性排斥反应给肺移植带来了重大障碍。尽管关于肺移植后气道上皮作用的证据仍在不断涌现,但它的重要性正日益受到重视。本综述探讨了气道上皮在各种移植后并发症中的复杂作用,同时强调了气道上皮培养作为一种研究模型的实用性。总之,通过阐明气道上皮在每种移植后并发症中的作用,并解释这些复杂的过程,本综述旨在为提高肺移植效果和改善患者护理的具体未来研究工作和治疗策略提供指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9df/11600126/b5c69d25db4c/ERR-0093-2024.02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9df/11600126/8eb251846f20/ERR-0093-2024.01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9df/11600126/b5c69d25db4c/ERR-0093-2024.02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9df/11600126/8eb251846f20/ERR-0093-2024.01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9df/11600126/b5c69d25db4c/ERR-0093-2024.02.jpg

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1
Airway epithelium in lung transplantation: a potential actor for post-transplant complications?肺移植中的气道上皮:移植后并发症的潜在因素?
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本文引用的文献

1
Cell Culture Differentiation and Proliferation Conditions Influence the Regeneration of the Human Airway Epithelium.细胞培养分化和增殖条件影响人呼吸道上皮的再生。
Am J Respir Cell Mol Biol. 2024 Sep;71(3):267-281. doi: 10.1165/rcmb.2023-0356MA.
2
Opportunistic Infections Post-Lung Transplantation: Viral, Fungal, and Mycobacterial.肺移植术后机会性感染:病毒、真菌和分枝杆菌。
Infect Dis Clin North Am. 2024 Mar;38(1):121-147. doi: 10.1016/j.idc.2023.12.001.
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Infections in Heart and Lung Transplant Recipients.心脏和肺移植受者的感染。
Infect Dis Clin North Am. 2024 Mar;38(1):103-120. doi: 10.1016/j.idc.2023.11.003.
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Recent advances in lung organoid development and applications in disease modeling.肺类器官的最新进展及其在疾病建模中的应用。
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Modulation of innate immunity in airway epithelium for host-directed therapy.气道上皮固有免疫的调控:宿主导向治疗策略。
Front Immunol. 2023 May 12;14:1197908. doi: 10.3389/fimmu.2023.1197908. eCollection 2023.
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Pulmonary epithelial markers in phenotypes of chronic lung allograft dysfunction.慢性肺移植功能障碍表型中的肺上皮标志物。
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Lymphocytic Airway Inflammation in Lung Allografts.肺移植中的淋巴细胞性气道炎症。
Front Immunol. 2022 Jul 12;13:908693. doi: 10.3389/fimmu.2022.908693. eCollection 2022.
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Incidence and risk factors of anastomotic complications after lung transplantation.肺移植术后吻合口并发症的发生率及危险因素。
Ther Adv Respir Dis. 2022 Jan-Dec;16:17534666221110354. doi: 10.1177/17534666221110354.
9
Respiratory Syncytial Virus, Human Metapneumovirus, and Parainfluenza Virus Infections in Lung Transplant Recipients: A Systematic Review of Outcomes and Treatment Strategies.肺移植受者中呼吸道合胞病毒、人类偏肺病毒和副流感病毒感染:结局和治疗策略的系统评价。
Clin Infect Dis. 2022 Jul 6;74(12):2252-2260. doi: 10.1093/cid/ciab969.
10
Lung Allograft Epithelium DNA Methylation Age Is Associated With Graft Chronologic Age and Primary Graft Dysfunction.肺移植上皮细胞 DNA 甲基化年龄与移植物时龄和原发性移植物功能障碍相关。
Front Immunol. 2021 Oct 7;12:704172. doi: 10.3389/fimmu.2021.704172. eCollection 2021.