Elodie Bernhard, Hamza Sakhi, Julie Oniszczuk, Constance Guillaud, Nicolas Limal, Ines Allioua, Narindra Jouan, Stephanie Guillet, Carine Diet, Bertrand Godeau, Philippe Remy, Vincent Audard, Nizar Joher, Anissa Moktefi
{"title":"靶抗原鉴定时代膜性狼疮性肾炎的重复活检。","authors":"Elodie Bernhard, Hamza Sakhi, Julie Oniszczuk, Constance Guillaud, Nicolas Limal, Ines Allioua, Narindra Jouan, Stephanie Guillet, Carine Diet, Bertrand Godeau, Philippe Remy, Vincent Audard, Nizar Joher, Anissa Moktefi","doi":"10.1007/s00428-025-04157-8","DOIUrl":null,"url":null,"abstract":"<p><p>In membranous lupus nephritis (LN), positivity for the target antigen exostosin 1/2 (EXT) is associated with a lower chronicity index (CI) at first biopsy and a lower risk of progression to end-stage kidney disease (ESKD) compared to EXT-negative patients. Repeat kidney biopsies (RKB) in LN may reveal increasing CI and class transition with prognostic significance. In a cohort of membranous LN with RKB, we assessed the variation in EXT and neural cell adhesion molecule 1 (NCAM1) expression and their association with class III/IV + V transition and renal outcomes. Thirty patients with 78 biopsies were enrolled. Index biopsies included 60% EXT-NCAM1-, 34% EXT + NCAM1-, 3% EXT-NCAM1 + and 3% EXT + NCAM1 + cases. Target antigen switch occurred in 3 (10%) cases (2 EXT + to EXT-; 1 NCAM1- to NCAM1 +) with favorable renal outcomes. EXT-positive and EXT-negative groups had similar clinico-pathological characteristics at baseline and at the end of follow-up, with comparable numbers of RKB, median CI increase, class transition rates, and renal outcomes. After a median follow-up of 8.8 years, 9 (32%) patients developed ESKD or glomerular filtration rate decrease > 40%. These patients exhibited higher median first biopsy CI (p = 0.04) and higher median serum creatinine level (p = 0.01), higher median CI (p = 0.02), and higher thrombotic microangiopathy (TMA) rate (p = 0.03) at second biopsy. TMA on any follow-up biopsy was more frequent in the adverse outcome group (p = 0.001). Not only EXT but also NCAM1 expression may vary in RKB during membranous LN. EXT-positive and EXT-negative patients had similar presentation and course, while TMA and CI compromised renal outcomes.</p>","PeriodicalId":23514,"journal":{"name":"Virchows Archiv","volume":" ","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2025-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Repeat biopsies in membranous lupus nephritis in the era of target antigen identification.\",\"authors\":\"Elodie Bernhard, Hamza Sakhi, Julie Oniszczuk, Constance Guillaud, Nicolas Limal, Ines Allioua, Narindra Jouan, Stephanie Guillet, Carine Diet, Bertrand Godeau, Philippe Remy, Vincent Audard, Nizar Joher, Anissa Moktefi\",\"doi\":\"10.1007/s00428-025-04157-8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>In membranous lupus nephritis (LN), positivity for the target antigen exostosin 1/2 (EXT) is associated with a lower chronicity index (CI) at first biopsy and a lower risk of progression to end-stage kidney disease (ESKD) compared to EXT-negative patients. Repeat kidney biopsies (RKB) in LN may reveal increasing CI and class transition with prognostic significance. In a cohort of membranous LN with RKB, we assessed the variation in EXT and neural cell adhesion molecule 1 (NCAM1) expression and their association with class III/IV + V transition and renal outcomes. Thirty patients with 78 biopsies were enrolled. Index biopsies included 60% EXT-NCAM1-, 34% EXT + NCAM1-, 3% EXT-NCAM1 + and 3% EXT + NCAM1 + cases. Target antigen switch occurred in 3 (10%) cases (2 EXT + to EXT-; 1 NCAM1- to NCAM1 +) with favorable renal outcomes. EXT-positive and EXT-negative groups had similar clinico-pathological characteristics at baseline and at the end of follow-up, with comparable numbers of RKB, median CI increase, class transition rates, and renal outcomes. After a median follow-up of 8.8 years, 9 (32%) patients developed ESKD or glomerular filtration rate decrease > 40%. These patients exhibited higher median first biopsy CI (p = 0.04) and higher median serum creatinine level (p = 0.01), higher median CI (p = 0.02), and higher thrombotic microangiopathy (TMA) rate (p = 0.03) at second biopsy. TMA on any follow-up biopsy was more frequent in the adverse outcome group (p = 0.001). Not only EXT but also NCAM1 expression may vary in RKB during membranous LN. EXT-positive and EXT-negative patients had similar presentation and course, while TMA and CI compromised renal outcomes.</p>\",\"PeriodicalId\":23514,\"journal\":{\"name\":\"Virchows Archiv\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2025-07-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Virchows Archiv\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s00428-025-04157-8\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PATHOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Virchows Archiv","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s00428-025-04157-8","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PATHOLOGY","Score":null,"Total":0}
Repeat biopsies in membranous lupus nephritis in the era of target antigen identification.
In membranous lupus nephritis (LN), positivity for the target antigen exostosin 1/2 (EXT) is associated with a lower chronicity index (CI) at first biopsy and a lower risk of progression to end-stage kidney disease (ESKD) compared to EXT-negative patients. Repeat kidney biopsies (RKB) in LN may reveal increasing CI and class transition with prognostic significance. In a cohort of membranous LN with RKB, we assessed the variation in EXT and neural cell adhesion molecule 1 (NCAM1) expression and their association with class III/IV + V transition and renal outcomes. Thirty patients with 78 biopsies were enrolled. Index biopsies included 60% EXT-NCAM1-, 34% EXT + NCAM1-, 3% EXT-NCAM1 + and 3% EXT + NCAM1 + cases. Target antigen switch occurred in 3 (10%) cases (2 EXT + to EXT-; 1 NCAM1- to NCAM1 +) with favorable renal outcomes. EXT-positive and EXT-negative groups had similar clinico-pathological characteristics at baseline and at the end of follow-up, with comparable numbers of RKB, median CI increase, class transition rates, and renal outcomes. After a median follow-up of 8.8 years, 9 (32%) patients developed ESKD or glomerular filtration rate decrease > 40%. These patients exhibited higher median first biopsy CI (p = 0.04) and higher median serum creatinine level (p = 0.01), higher median CI (p = 0.02), and higher thrombotic microangiopathy (TMA) rate (p = 0.03) at second biopsy. TMA on any follow-up biopsy was more frequent in the adverse outcome group (p = 0.001). Not only EXT but also NCAM1 expression may vary in RKB during membranous LN. EXT-positive and EXT-negative patients had similar presentation and course, while TMA and CI compromised renal outcomes.
期刊介绍:
Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.