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诊断抗体介导排斥反应的挑战:侵袭性和非侵袭性生物标志物的作用。

Challenges of Diagnosing Antibody-Mediated Rejection: The Role of Invasive and Non-Invasive Biomarkers.

机构信息

Division of Nephrology, The University of Chicago Medical Center, Chicago, IL 60637, USA.

出版信息

Medicina (Kaunas). 2021 May 3;57(5):439. doi: 10.3390/medicina57050439.

DOI:10.3390/medicina57050439
PMID:34063583
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8147623/
Abstract

Kidney transplantation is the best treatment modality for end-stage kidney disease, leading to improvement in a patient's quality and quantity of life. With significant improvements in short-term outcomes, prolonging long-term allograft and patient survival remain ongoing challenges. The ability to monitor allograft function, immune tolerance and predict rejection accurately would enable personalization and better prognostication during post-transplant care. Though kidney biopsy remains the backbone of transplant diagnostics, emerging biomarkers can help detecting kidney allograft injury early enough to prevent permanent damage and detect injury before it is clinically apparent. In this review, we summarize the recent biomarkers that have shown promise in the prediction of acute rejection with a focus on antibody-mediated rejection in kidney transplantation.

摘要

肾移植是治疗终末期肾病的最佳方法,可改善患者的生活质量和数量。随着短期结果的显著改善,延长长期移植物和患者的生存仍然是持续存在的挑战。能够准确监测移植物功能、免疫耐受和预测排斥反应将使移植后护理期间的个性化和更好的预后成为可能。虽然肾活检仍然是移植诊断的基础,但新兴的生物标志物可以帮助早期发现肾移植损伤,以防止永久性损伤,并在临床上出现之前检测到损伤。在这篇综述中,我们总结了最近在预测急性排斥反应方面显示出前景的生物标志物,重点是肾移植中的抗体介导的排斥反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d19/8147623/49ccee2b1b0d/medicina-57-00439-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d19/8147623/49ccee2b1b0d/medicina-57-00439-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d19/8147623/49ccee2b1b0d/medicina-57-00439-g001.jpg

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本文引用的文献

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Discovery and Validation of a Urinary Exosome mRNA Signature for the Diagnosis of Human Kidney Transplant Rejection.用于诊断人类肾移植排斥反应的尿液外泌体mRNA特征的发现与验证
J Am Soc Nephrol. 2021 Apr;32(4):994-1004. doi: 10.1681/ASN.2020060850. Epub 2021 Mar 3.
2
Long-term kidney transplant graft survival-Making progress when most needed.长期肾移植移植物存活率——最需要时取得进展。
Am J Transplant. 2021 Aug;21(8):2824-2832. doi: 10.1111/ajt.16463. Epub 2021 Feb 8.
3
C1q-binding DSA and allograft outcomes in pediatric kidney transplant recipients.
细胞外囊泡:肺移植受者抗体介导排斥反应中一个潜在的新因素。
Front Transplant. 2023 Sep 4;2:1248987. doi: 10.3389/frtra.2023.1248987. eCollection 2023.
4
An Antibody-Aptamer-Hybrid Lateral Flow Assay for Detection of CXCL9 in Antibody-Mediated Rejection after Kidney Transplantation.一种用于检测肾移植后抗体介导排斥反应中CXCL9的抗体-适配体杂交侧流分析方法。
Diagnostics (Basel). 2022 Jan 25;12(2):308. doi: 10.3390/diagnostics12020308.
C1q 结合型 dsDNA 与儿童肾移植受者的移植物结局。
Pediatr Transplant. 2021 Mar;25(2):e13885. doi: 10.1111/petr.13885. Epub 2020 Nov 1.
4
The role of non-HLA antibodies in solid organ transplantation: a complex deliberation.非 HLA 抗体在实体器官移植中的作用:一个复杂的考量。
Curr Opin Organ Transplant. 2020 Dec;25(6):536-542. doi: 10.1097/MOT.0000000000000811.
5
Diagnostic performance of kSORT, a blood-based mRNA assay for noninvasive detection of rejection after kidney transplantation: A retrospective multicenter cohort study.基于血液的 kSORT mRNA 检测在肾移植后非侵入性排斥反应诊断中的性能:一项回顾性多中心队列研究。
Am J Transplant. 2021 Feb;21(2):740-750. doi: 10.1111/ajt.16179. Epub 2020 Aug 4.
6
Angiotensin II Type 1 Receptor Expression in Renal Transplant Biopsies and Anti-AT1R Antibodies in Serum Indicates the Risk of Transplant Loss.肾移植活检中血管紧张素II 1型受体表达及血清中抗AT1R抗体提示移植肾丢失风险。
Transplant Proc. 2020 Oct;52(8):2299-2304. doi: 10.1016/j.transproceed.2020.01.126. Epub 2020 May 21.
7
High levels of dd-cfDNA identify patients with TCMR 1A and borderline allograft rejection at elevated risk of graft injury.高水平的 dd-cfDNA 可识别 1A 型 TCMR 和边缘供体排斥反应患者,这些患者有发生移植物损伤的高风险。
Am J Transplant. 2020 Sep;20(9):2491-2498. doi: 10.1111/ajt.15822. Epub 2020 Mar 10.
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EBioMedicine. 2019 Aug;46:463-472. doi: 10.1016/j.ebiom.2019.07.028. Epub 2019 Aug 1.
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Long-Term Outcomes after Acute Rejection in Kidney Transplant Recipients: An ANZDATA Analysis.肾移植受者急性排斥反应后的长期结局:ANZDATA 分析。
J Am Soc Nephrol. 2019 Sep;30(9):1697-1707. doi: 10.1681/ASN.2018111101. Epub 2019 Jul 15.