Evidence map›Paper›PMID 42382225›Full record

ArticleTransplant international : official journal of the European Society for Organ Transplantation2026

Not all antibodies are created equal: total IgG glycosylation and severity of antibody-mediated rejection in kidney transplantation.

Johan Noble, Leandre M Glendenning, Celine Dard, Anne Bourdin, Marta Crespo, Umberto Maggiore, Ari R Inwood, Grace C Carlson, Brian A Cobb, Paolo Cravedi

Abstract readMulticenter Study
In one paragraph

Article in Transplant international : official journal of the European Society for Organ Transplantation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Johan Noble *Translational Transplant Research Center (TTRC), Icahn School of Medicine at Mount Sinai, Precision Immunology Institute, New York, NY, United States.
Leandre M Glendenning *Department of Pathology, Case Western Reserve University School of Medicine, Cleveland, OH, United States.
Celine DardEtablissement Français du Sang, Grenoble-Alpes, France.
Anne BourdinEtablissement Français du Sang, Grenoble-Alpes, France.
Marta CrespoDepartment of Nephrology, Hospital Ddel Mar, Nephropathies Research Group, Hospital del Mar Research Institute, Barcelona, Spain.
Umberto MaggioreNephrology Unit, Department of Medicine and Surgery, University Hospital of Parma, Parma, Italy.
Ari R InwoodDepartment of Pathology, Case Western Reserve University School of Medicine, Cleveland, OH, United States.
Grace C CarlsonDepartment of Pathology, Case Western Reserve University School of Medicine, Cleveland, OH, United States.
Brian A CobbDepartment of Pathology, Case Western Reserve University School of Medicine, Cleveland, OH, United States.
Paolo CravediTranslational Transplant Research Center (TTRC), Icahn School of Medicine at Mount Sinai, Precision Immunology Institute, New York, NY, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antibody-mediated rejection (AMR) is a leading cause of kidney transplant failure and is primarily driven by donor-specific anti-HLA antibodies (DSA), although DSA presence alone does not fully explain the heterogeneity of AMR severity. We prospectively studied 79 kidney transplant recipients from 2 European centers, including 29 with active AMR (aAMR), 29 with chronic-active AMR (caAMR), and 21 controls without rejection, to investigate the association between total Immunoglobulin-G (IgG) glycosylation profiles and AMR. IgG glycosylation was quantified using lectin-based ELISA, assessing relative levels of mannose, core fucose, α2,6-linked sialic acid, and bisecting N-acetylglucosamine (GlcNAc). Bisecting GlcNAc levels were higher in caAMR compared with controls and aAMR (both p < 0.001), while core fucosylation and mannose levels were increased in aAMR and caAMR relative to controls. Higher levels of core fucose, mannose, and α2,6-sialylation were associated with increasing glomerulitis severity. We found that bisecting GlcNAc (PHA-E/Fc) was significantly associated with both higher g- and cg-score (in ordinal models, OR = 2.1 [95% CI: 1.2-4.1; p = 0.017], and OR = 2.0 [95% CI: 1.1-4.3; p = 0.046], respectively). Mannose level (ConA/Fc) was significantly associated with higher g-score (2.1 [1.1-4.2], p = 0.017]). These findings indicate that distinct total IgG glycosylation features are independently associated with specific histological patterns of AMR severity.

Indexed as

Graft RejectionImmunoglobulin GIsoantibodiesKidney TransplantationAcetylglucosamineAdultEnzyme-Linked Immunosorbent AssayFemaleGlycosylationHLA AntigensHumansMaleMiddle AgedProspective StudiesAcetylglucosamineHLA AntigensImmunoglobulin GIsoantibodiesantibody-mediated rejectionglycosylationimmunoglobulin GN-acetylglucosaminerenal transplant

Identifiers

PMID42382225
PMCPMC13315302

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Registered trials

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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.