Evidence map›Paper›PMID 42048157›Full record

Observational studyThe Journal of clinical investigation2026

Anti-nephrin antibodies are not enriched in patients with primary and posttransplant recurrent podocytopathies.

Francesco Pecoraro, Luca Perico, Federica Casiraghi, Paola Rizzo, Matias Trillini, Andrea Angeletti, Manuel Alfredo Podestà, Xhuliana Kajana, Agnese Spennacchio, Marta Todeschini and 4 more

Registry-linked trialAbstract readObservational Study
In one paragraph

Observational study in The Journal of clinical investigation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06334692 (Autoantibodies Against-nephrin in Idiopathic Nephrotic Syndrome), which is not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT06334692 recruitingnot on this map

Autoantibodies Against-nephrin in Idiopathic Nephrotic Syndrome

TypeobservationalSponsorMario Negri Institute for Pharmacological ResearchRan2024 to 2028Enrolled100ConditionsNephrotic SyndromeArmsIn-house ELISA, and ELISA kits from "DBA Italy" (Abbexa).
3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Nephrin autoimmunity: signal, noise, and a path to clarity.The Journal of clinical investigation · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Francesco PecoraroDepartment of Molecular Medicine and.
Luca PericoDepartment of Molecular Medicine and.
Federica CasiraghiDepartment of Molecular Medicine and.
Paola RizzoDepartment of Molecular Medicine and.
Matias TrilliniClinical Research Center for Rare Diseases "Aldo e Cele Daccò," Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Bergamo, Italy.
Andrea AngelettiDivision of Nephrology, Dialysis, and Transplantation, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Manuel Alfredo PodestàRenal Research Laboratory, Unit of Nephrology, Dialysis, and Renal Transplantation, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Xhuliana KajanaDivision of Nephrology, Dialysis, and Transplantation, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Agnese SpennacchioDivision of Nephrology, Dialysis, and Transplantation, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Marta TodeschiniDepartment of Molecular Medicine and.
Marilena MisterDepartment of Molecular Medicine and.
Giuseppe CastellanoRenal Research Laboratory, Unit of Nephrology, Dialysis, and Renal Transplantation, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Ariela BenigniDepartment of Molecular Medicine and.
Giuseppe RemuzziDepartment of Molecular Medicine and.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUNDAnti-nephrin autoantibodies have emerged as a putative pathogenic driver in a subset of patients with podocytopathies, including those with posttransplant disease recurrence.METHODSWe measured anti-nephrin autoantibodies in a cohort of 65 patients with podocytopathy associated with steroid-sensitive nephrotic syndrome (n = 39) and steroid-resistant nephrotic syndrome (n = 26) and in 34 patients with posttransplant podocytopathy recurrence. Fourteen patients with membranous nephropathy and 20 healthy volunteers served as controls. ELISA and immunoprecipitation assays were performed to detect anti-nephrin IgG using 2 different recombinant human nephrin proteins. Immunofluorescence analysis was performed to assess gG deposition and its colocalization with nephrin in renal biopsies.RESULTSWhen using an ELISA based on murine cell-derived human antigen, the highest positivity was found in healthy volunteers (55%), correlating with levels of circulating natural anti-α-galactose-α-1,3-galactose antibodies. This cross-reactivity was abrogated with recombinant human nephrin expressed in human cells. In this setting, very low prevalence (<5%) of anti-nephrin antibody-positive patients was found in steroid-sensitive and -resistant nephrotic syndrome cohorts and in patients with posttransplant disease recurrence. These frequencies were comparable to healthy volunteers. Using confocal and super-resolution microscopy, only trace amounts of IgM, but no IgG, were found in the glomeruli of analyzed biopsies, which did not colocalize with nephrin.CONCLUSIONWith the methodology presented here, anti-nephrin reactivity was extremely rare and occurred at comparably low frequencies in healthy controls, native-kidney podocytopathies, and posttransplant disease recurrence. This suggests that these autoantibodies are not inherently disease specific and may not serve as a broad biomarker across podocytopathies.TRIAL REGISTRATIONClinicalTrials.gov NCT06334692.FUNDINGThe Medici di Marignano family.

Indexed as

AutoantibodiesKidney TransplantationMembrane ProteinsNephrotic SyndromePodocytesAdultAnimalsCase-Control StudiesFemaleGlomerulonephritis, MembranousHumansMaleMiddle AgedRecurrenceAutoantibodiesMembrane ProteinsnephrinAutoimmunityImmunoglobulinsNephrology

Identifiers

PMID42048157
PMCPMC13318109

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.