Katelynn S. Madill-Thomsen , Luis G. Hidalgo , Zachary P. Demko , Philippe M. Gauthier , Adam Prewett , Dave Lowe , Jessica J. Chang , Martina Mackova , Klemens Budde , Jonathan S. Bromberg , Philip F. Halloran
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Halloran","doi":"10.1016/j.ekir.2025.06.017","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><div>Effective therapies for kidney transplant antibody-mediated rejection (ABMR) will require accurate diagnoses plus assessment of ABMR activity, and the new tests that were used to show treatment effects in the clinical trial such as donor-derived cell-free DNA (dd-cfDNA) and molecular biopsy analysis (the Molecular Microscope Diagnostic System) could be useful.</div></div><div><h3>Methods</h3><div>Trifecta-Kidney (<span><span>ClinicalTrials.gov</span><svg><path></path></svg></span> #NCT04239703) studied 717 indication biopsies to define the relationships among the following 4 tests used for ABMR: (i) standard-of-care (SOC) local histologic biopsy ABMR diagnosis, (ii) MMDx ABMR diagnosis, (iii) dd-cfDNA, and (iv) donor-specific antibody (DSA).</div></div><div><h3>Results</h3><div>All 4 tests were correlated in a partial correlation network, with a hierarchy of intertest correlations: MMDx ABMR > dd-cfDNA > histology ABMR > DSA. Surprisingly, DSA correlated at least as strongly with MMDx ABMR as with histologic ABMR, even though DSA is not used in MMDx. When expressed in the same 6 rejection classes, MMDx diagnosed ABMR more frequently than histology. When histology disagreed with MMDx ABMR, dd-cfDNA and DSA correlated more strongly with MMDx assessment. However, histology also detected ABMR lesions in some cases that MMDx called No Rejection, correlating with subthreshold molecular ABMR activity, dd-cfDNA and DSA (AJT 25:72-87, 2024). Molecular rejection predicted graft outcomes better than histologic rejection in Trifecta-Kidney, and this finding was confirmed in the earlier INTERCOMEX study cohort.</div></div><div><h3>Discussion</h3><div>The 4-way intertest correlations extend below current thresholds for diagnosing ABMR. These results map a network of 4 ABMR-related tests that can add precision to ABMR assessment in trials and clinical management, and highlight the need to establish the clinical significance of subthreshold ABMR activity.</div></div>","PeriodicalId":17761,"journal":{"name":"Kidney International Reports","volume":"10 9","pages":"Pages 3225-3238"},"PeriodicalIF":5.7000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Defining Relationships Among Tests for Kidney Transplant Antibody-Mediated Rejection\",\"authors\":\"Katelynn S. Madill-Thomsen , Luis G. Hidalgo , Zachary P. Demko , Philippe M. Gauthier , Adam Prewett , Dave Lowe , Jessica J. Chang , Martina Mackova , Klemens Budde , Jonathan S. Bromberg , Philip F. Halloran\",\"doi\":\"10.1016/j.ekir.2025.06.017\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction</h3><div>Effective therapies for kidney transplant antibody-mediated rejection (ABMR) will require accurate diagnoses plus assessment of ABMR activity, and the new tests that were used to show treatment effects in the clinical trial such as donor-derived cell-free DNA (dd-cfDNA) and molecular biopsy analysis (the Molecular Microscope Diagnostic System) could be useful.</div></div><div><h3>Methods</h3><div>Trifecta-Kidney (<span><span>ClinicalTrials.gov</span><svg><path></path></svg></span> #NCT04239703) studied 717 indication biopsies to define the relationships among the following 4 tests used for ABMR: (i) standard-of-care (SOC) local histologic biopsy ABMR diagnosis, (ii) MMDx ABMR diagnosis, (iii) dd-cfDNA, and (iv) donor-specific antibody (DSA).</div></div><div><h3>Results</h3><div>All 4 tests were correlated in a partial correlation network, with a hierarchy of intertest correlations: MMDx ABMR > dd-cfDNA > histology ABMR > DSA. Surprisingly, DSA correlated at least as strongly with MMDx ABMR as with histologic ABMR, even though DSA is not used in MMDx. When expressed in the same 6 rejection classes, MMDx diagnosed ABMR more frequently than histology. When histology disagreed with MMDx ABMR, dd-cfDNA and DSA correlated more strongly with MMDx assessment. However, histology also detected ABMR lesions in some cases that MMDx called No Rejection, correlating with subthreshold molecular ABMR activity, dd-cfDNA and DSA (AJT 25:72-87, 2024). Molecular rejection predicted graft outcomes better than histologic rejection in Trifecta-Kidney, and this finding was confirmed in the earlier INTERCOMEX study cohort.</div></div><div><h3>Discussion</h3><div>The 4-way intertest correlations extend below current thresholds for diagnosing ABMR. These results map a network of 4 ABMR-related tests that can add precision to ABMR assessment in trials and clinical management, and highlight the need to establish the clinical significance of subthreshold ABMR activity.</div></div>\",\"PeriodicalId\":17761,\"journal\":{\"name\":\"Kidney International Reports\",\"volume\":\"10 9\",\"pages\":\"Pages 3225-3238\"},\"PeriodicalIF\":5.7000,\"publicationDate\":\"2025-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Kidney International Reports\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2468024925003870\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"UROLOGY & NEPHROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Kidney International Reports","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2468024925003870","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"UROLOGY & NEPHROLOGY","Score":null,"Total":0}
Defining Relationships Among Tests for Kidney Transplant Antibody-Mediated Rejection
Introduction
Effective therapies for kidney transplant antibody-mediated rejection (ABMR) will require accurate diagnoses plus assessment of ABMR activity, and the new tests that were used to show treatment effects in the clinical trial such as donor-derived cell-free DNA (dd-cfDNA) and molecular biopsy analysis (the Molecular Microscope Diagnostic System) could be useful.
Methods
Trifecta-Kidney (ClinicalTrials.gov #NCT04239703) studied 717 indication biopsies to define the relationships among the following 4 tests used for ABMR: (i) standard-of-care (SOC) local histologic biopsy ABMR diagnosis, (ii) MMDx ABMR diagnosis, (iii) dd-cfDNA, and (iv) donor-specific antibody (DSA).
Results
All 4 tests were correlated in a partial correlation network, with a hierarchy of intertest correlations: MMDx ABMR > dd-cfDNA > histology ABMR > DSA. Surprisingly, DSA correlated at least as strongly with MMDx ABMR as with histologic ABMR, even though DSA is not used in MMDx. When expressed in the same 6 rejection classes, MMDx diagnosed ABMR more frequently than histology. When histology disagreed with MMDx ABMR, dd-cfDNA and DSA correlated more strongly with MMDx assessment. However, histology also detected ABMR lesions in some cases that MMDx called No Rejection, correlating with subthreshold molecular ABMR activity, dd-cfDNA and DSA (AJT 25:72-87, 2024). Molecular rejection predicted graft outcomes better than histologic rejection in Trifecta-Kidney, and this finding was confirmed in the earlier INTERCOMEX study cohort.
Discussion
The 4-way intertest correlations extend below current thresholds for diagnosing ABMR. These results map a network of 4 ABMR-related tests that can add precision to ABMR assessment in trials and clinical management, and highlight the need to establish the clinical significance of subthreshold ABMR activity.
期刊介绍:
Kidney International Reports, an official journal of the International Society of Nephrology, is a peer-reviewed, open access journal devoted to the publication of leading research and developments related to kidney disease. With the primary aim of contributing to improved care of patients with kidney disease, the journal will publish original clinical and select translational articles and educational content related to the pathogenesis, evaluation and management of acute and chronic kidney disease, end stage renal disease (including transplantation), acid-base, fluid and electrolyte disturbances and hypertension. Of particular interest are submissions related to clinical trials, epidemiology, systematic reviews (including meta-analyses) and outcomes research. The journal will also provide a platform for wider dissemination of national and regional guidelines as well as consensus meeting reports.