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扩大微血管炎症的范围:揭示其在抗体介导排斥反应之外于T细胞介导环境中的存在。

Expanding the Scope of Microvascular Inflammation: Unveiling Its Presence Beyond Antibody-Mediated Rejection Into T-Cell Mediated Contexts.

作者信息

Varol Hilal, Wagenmakers Anne, Hoeft Konrad, Callemeyn Jasper, Bodewes Roos, Bramer Wichor, Stubbs Andrew, Kramann Rafael, Naesens Maarten, Clahsen-Van Groningen Marian C

机构信息

Department of Pathology, Erasmus Medical Center Rotterdam, Rotterdam, Netherlands.

Erasmus MC Transplant Institute, University Medical Center Rotterdam, Rotterdam, Netherlands.

出版信息

Transpl Int. 2025 Jan 6;37:13464. doi: 10.3389/ti.2024.13464. eCollection 2024.

DOI:10.3389/ti.2024.13464
PMID:39834692
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11742949/
Abstract

Microvascular inflammation (MVI) in kidney transplant biopsies is mainly associated with antibody-mediated rejection (AMR), sparking debate within the Banff Classification of Renal Allograft Pathology regarding its exclusivity. This study reviewed the literature on MVI in T cell-mediated rejection (TCMR) and analyzed MVI in our transplant population. We searched English publications in MEDLINE, Embase, Web of Science, Cochrane, and Google Scholar until June 2024, focusing on glomerulitis (g), peritubular capillaritis (ptc), or MVI in kidney transplant biopsies classified as TCMR. Additionally, we examined g, ptc, and MVI in 69 patients with AMR, TCMR, and no rejection. Our search yielded 541 citations, with 10 studies included, covering 810 TCMR and 156 AMR biopsies. The studies showed g, ptc, and MVI were present in TCMR but were less prevalent and severe than in AMR. In our cohort, AMR had significantly higher g, ptc, and MVI scores compared to aTCMR and ATN, however, aTCMR also displayed MVI. These findings confirm that MVI occurs in aTCMR and should not be exclusively linked to AMR. These findings highlight the need to further explore MVI's significance in TCMR and investigate the inflammatory composition. This could refine the Banff Classification, improving Classification accuracy of kidney transplant pathology assessments.

摘要

肾移植活检中的微血管炎症(MVI)主要与抗体介导的排斥反应(AMR)相关,这在肾移植病理的班夫分类中引发了关于其排他性的争论。本研究回顾了关于T细胞介导的排斥反应(TCMR)中MVI的文献,并分析了我们移植人群中的MVI。我们检索了截至2024年6月在MEDLINE、Embase、科学网、Cochrane和谷歌学术上的英文出版物,重点关注肾移植活检中分类为TCMR的肾小球炎(g)、肾小管周围毛细血管炎(ptc)或MVI。此外,我们检查了69例发生AMR、TCMR和无排斥反应患者的g、ptc和MVI。我们的检索产生了541条引用,纳入了10项研究,涵盖810例TCMR活检和156例AMR活检。研究表明,g、ptc和MVI在TCMR中存在,但比在AMR中更不常见且严重程度更低。在我们的队列中,与急性TCMR和急性肾小管坏死相比,AMR的g、ptc和MVI评分显著更高,然而,急性TCMR也表现出MVI。这些发现证实MVI发生在急性TCMR中,不应仅与AMR相关联。这些发现强调需要进一步探索MVI在TCMR中的意义并研究炎症成分。这可以完善班夫分类,提高肾移植病理评估的分类准确性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d5d/11742949/4178738e7582/ti-37-13464-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d5d/11742949/939ee1d1e993/ti-37-13464-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d5d/11742949/51197fef065a/ti-37-13464-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d5d/11742949/4178738e7582/ti-37-13464-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d5d/11742949/939ee1d1e993/ti-37-13464-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d5d/11742949/51197fef065a/ti-37-13464-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d5d/11742949/4178738e7582/ti-37-13464-g003.jpg

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本文引用的文献

1
The Banff 2022 Kidney Meeting Report: Reappraisal of microvascular inflammation and the role of biopsy-based transcript diagnostics.班夫 2022 年肾脏会议报告:重新评估微血管炎症和基于活检的转录诊断学的作用。
Am J Transplant. 2024 Mar;24(3):338-349. doi: 10.1016/j.ajt.2023.10.016. Epub 2023 Oct 28.
2
Transcriptional and spatial profiling of the kidney allograft unravels a central role for FcyRIII+ innate immune cells in rejection.对肾移植的转录和空间分析揭示了 FcyRIII+固有免疫细胞在排斥反应中的核心作用。
Nat Commun. 2023 Jul 19;14(1):4359. doi: 10.1038/s41467-023-39859-7.
3
The Molecular Phenotype of Kidney Transplants: Insights From the MMDx Project.
肾脏移植的分子表型:来自 MMDx 项目的见解。
Transplantation. 2024 Jan 1;108(1):45-71. doi: 10.1097/TP.0000000000004624. Epub 2023 Dec 13.
4
Feasibility and Potential of Transcriptomic Analysis Using the NanoString nCounter Technology to Aid the Classification of Rejection in Kidney Transplant Biopsies.使用 NanoString nCounter 技术进行转录组分析辅助肾移植活检排斥分类的可行性和潜力。
Transplantation. 2023 Apr 1;107(4):903-912. doi: 10.1097/TP.0000000000004372. Epub 2022 Oct 27.
5
Causes of Kidney Graft Failure in a Cohort of Recipients With a Very Long-Time Follow-Up After Transplantation.一组移植后长期随访受者肾移植失败的原因
Front Med (Lausanne). 2022 Jun 6;9:842419. doi: 10.3389/fmed.2022.842419. eCollection 2022.
6
Association of HLA Mismatches and Histology Suggestive of Antibody-Mediated Injury in the Absence of Donor-Specific Anti-HLA Antibodies.在不存在供体特异性抗 HLA 抗体的情况下,HLA 错配与组织学表现提示抗体介导的损伤相关。
Clin J Am Soc Nephrol. 2022 Aug;17(8):1204-1215. doi: 10.2215/CJN.00570122. Epub 2022 Jun 1.
7
The PRISMA 2020 statement: an updated guideline for reporting systematic reviews.《PRISMA 2020声明:系统评价报告的更新指南》
Rev Esp Cardiol (Engl Ed). 2021 Sep;74(9):790-799. doi: 10.1016/j.rec.2021.07.010.
8
The evolution of histological changes suggestive of antibody-mediated injury, in the presence and absence of donor-specific anti-HLA antibodies.在存在和不存在供体特异性抗HLA抗体的情况下,提示抗体介导损伤的组织学变化的演变。
Transpl Int. 2021 Oct;34(10):1824-1836. doi: 10.1111/tri.13964. Epub 2021 Sep 12.
9
The Banff 2019 Kidney Meeting Report (I): Updates on and clarification of criteria for T cell- and antibody-mediated rejection.《2019 年班夫肾脏会议报告(一):T 细胞和抗体介导排斥反应标准的更新和澄清》。
Am J Transplant. 2020 Sep;20(9):2318-2331. doi: 10.1111/ajt.15898. Epub 2020 May 28.
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