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支气管肺泡灌洗细胞因子对于诊断肺移植后并发症的价值较小。

Bronchoalveolar lavage cytokines are of minor value to diagnose complications following lung transplantation.

机构信息

Division of Pulmonology, University Hospital Zurich, Rämistrasse 100, CH-8091 Zurich, Switzerland.

Clinic of Immunology, University Hospital Zurich, Gloriastrasse 23, CH-8091 Zurich, Switzerland.

出版信息

Cytokine. 2020 Jan;125:154794. doi: 10.1016/j.cyto.2019.154794. Epub 2019 Aug 7.

DOI:10.1016/j.cyto.2019.154794
PMID:31400641
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7128992/
Abstract

Early diagnosis and treatment of acute cellular rejection (ACR) may improve long-term outcome for lung transplant recipients (LTRs). Cytokines have become valuable diagnostic tools in many medical fields. The role of bronchoalveolar lavage (BAL) cytokines is of unknown value to diagnose ACR and distinguish rejection from infection. We hypothesized that distinct cytokine patterns obtained by surveillance bronchoscopies during the first year after transplantation are associated with ACR and microbiologic findings. We retrospectively analyzed data from 319 patients undergoing lung transplantation at University Hospital Zurich from 1998 to 2016. We compared levels of IL-6, IL-8, IFN-γ and TNF-α in 747 BAL samples with transbronchial biopsies (TBB) and microbiologic results from surveillance bronchoscopies. We aimed to define reference values that would allow distinction between four specific groups "ACR", "infection", "combined ACR and infection" and "no pathologic process". No definitive pattern was identified. Given the overlap between groups, these four cytokines are not suitable diagnostic markers for ACR or infection after lung transplantation.

摘要

早期诊断和治疗急性细胞排斥(ACR)可能改善肺移植受者(LTR)的长期预后。细胞因子已成为许多医学领域有价值的诊断工具。支气管肺泡灌洗(BAL)细胞因子在诊断 ACR 以及区分排斥反应与感染方面的作用尚不清楚。我们假设,在移植后第一年的监测性支气管镜检查中获得的不同细胞因子模式与 ACR 和微生物学发现有关。我们回顾性分析了 1998 年至 2016 年在苏黎世大学医院进行肺移植的 319 例患者的数据。我们比较了 747 例 BAL 样本与经支气管活检(TBB)以及监测性支气管镜检查的微生物学结果中 IL-6、IL-8、IFN-γ 和 TNF-α的水平。我们旨在确定参考值,以便区分“ACR”、“感染”、“ACR 和感染合并”和“无病理过程”四个特定组。没有确定明确的模式。鉴于各组之间存在重叠,这四种细胞因子不适合作为肺移植后 ACR 或感染的诊断标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2af8/7128992/c08ee50b273c/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2af8/7128992/13cc2f802388/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2af8/7128992/85905cfd6bcf/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2af8/7128992/c08ee50b273c/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2af8/7128992/13cc2f802388/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2af8/7128992/85905cfd6bcf/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2af8/7128992/c08ee50b273c/gr3_lrg.jpg

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本文引用的文献

1
Role of Mast Cells and Type 2 Innate Lymphoid (ILC2) Cells in Lung Transplantation.肥大细胞和 2 型先天淋巴样(ILC2)细胞在肺移植中的作用。
J Immunol Res. 2018 Oct 30;2018:2785971. doi: 10.1155/2018/2785971. eCollection 2018.
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Recent advances in lung transplantation.肺移植的最新进展
F1000Res. 2018 Oct 23;7. doi: 10.12688/f1000research.15393.1. eCollection 2018.
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Infections after lung transplantation.肺移植后的感染
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Sequential broncho-alveolar lavages reflect distinct pulmonary compartments: clinical and research implications in lung transplantation.序贯支气管肺泡灌洗反映了不同的肺区:肺移植的临床和研究意义。
Respir Res. 2018 May 25;19(1):102. doi: 10.1186/s12931-018-0786-z.
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The Immunomodulatory Effects of Macrolides-A Systematic Review of the Underlying Mechanisms.大环内酯类的免疫调节作用——潜在机制的系统评价。
Front Immunol. 2018 Mar 13;9:302. doi: 10.3389/fimmu.2018.00302. eCollection 2018.
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Acute rejection.急性排斥反应
J Thorac Dis. 2017 Dec;9(12):5440-5457. doi: 10.21037/jtd.2017.11.83.
7
Heparin-binding protein, lysozyme, and inflammatory cytokines in bronchoalveolar lavage fluid as diagnostic tools for pulmonary infection in lung transplanted patients.肝素结合蛋白、溶菌酶和炎症细胞因子在支气管肺泡灌洗液中作为肺移植患者肺部感染的诊断工具。
Am J Transplant. 2018 Feb;18(2):444-452. doi: 10.1111/ajt.14458. Epub 2017 Sep 15.
8
The Registry of the International Society for Heart and Lung Transplantation: Thirty-fourth Adult Lung And Heart-Lung Transplantation Report-2017; Focus Theme: Allograft ischemic time.国际心肺移植学会登记处:2017年第34次成人肺移植和心肺联合移植报告;重点主题:移植物缺血时间。
J Heart Lung Transplant. 2017 Oct;36(10):1047-1059. doi: 10.1016/j.healun.2017.07.016. Epub 2017 Jul 19.
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