Evidence map›Paper›PMID 25071157›Full record

ArticleMolecular & cellular proteomics : MCP2014

Identification of distinct glycoforms of IgA1 in plasma from patients with immunoglobulin A (IgA) nephropathy and healthy individuals.

Sylvain Lehoux, Rongjuan Mi, Rajindra P Aryal, Yingchun Wang, Katrine T-B G Schjoldager, Henrik Clausen, Irma van Die, Yoosun Han, Arlene B Chapman, Richard D Cummings and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.2field-weighted citation impact, top 22% of its field
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

23 citing papers in PubMed, 32 citations in OpenAlex.

  1. Trial
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  3. Review
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  5. Article
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  8. GermlineProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  9. Article
  10. Article
  11. Science advances · 2021
    Article
  12. Article
  13. History of IgA Nephropathy Mouse Models.Journal of clinical medicine · 2021
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. N-glycopeptide Signatures of IgAMolecular & cellular proteomics : MCP · 2019
    Article
  19. Article
  20. 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

11 authors at 3 institutions in 3 countries.

Sylvain LehouxFrom the Departments of ‡Biochemistry and.
Rongjuan MiFrom the Departments of ‡Biochemistry and.
Rajindra P AryalFrom the Departments of ‡Biochemistry and.
Yingchun WangFrom the Departments of ‡Biochemistry and.
Katrine T-B G Schjoldager§Department of Cellular and Molecular Medicine, Copenhagen Center for Glycomics, Copenhagen, Denmark;
Henrik Clausen§Department of Cellular and Molecular Medicine, Copenhagen Center for Glycomics, Copenhagen, Denmark;
Irma van Die¶Department of Molecular Cell Biology & Immunology, VU University Medical Center, Amsterdam, The Netherlands.
Yoosun Han‖Medicine, Emory University School of Medicine, Atlanta, GA 30322;
Arlene B Chapman‖Medicine, Emory University School of Medicine, Atlanta, GA 30322;
Richard D CummingsFrom the Departments of ‡Biochemistry and.
Tongzhong JuFrom the Departments of ‡Biochemistry and tju@emory.edu.
Emory University · USUniversity of Copenhagen · DKAmsterdam UMC Location VUmc · NL

Funding

Genetic Basis of Non-Familial IgA NephropathyR01DK080876 · NIDDK · EMORY UNIVERSITY · PI JU, TONGZHONG · 2008 to 2012
$1.5M
NIDDK NIH HHS R01 DK080876NIDDK NIH HHS R01DK80876
6 · The paper itself

Abstract

Immunoglobulin A nephropathy (IgAN) is the most common form of glomerulonephritis worldwide and is histologically characterized by the deposition of IgA1 and consequent inflammation in the glomerular mesangium. Prior studies suggested that serum IgA1 from IgAN patients contains aberrant, undergalactosylated O-glycans, for example, Tn antigen and its sialylated version, SialylTn (STn), but the mechanisms underlying aberrant O-glycosylation are not well understood. Here we have used serial lectin separation technologies, Western blot, enzymatic modifications, and mass spectrometry to explore whether there are different glycoforms of IgA1 in plasma from patients with IgAN and healthy individuals. Although total plasma IgA in IgAN patients was elevated ∼ 1.6-fold compared with that in healthy donors, IgA1 in all samples was unexpectedly separable into two distinct glycoforms: one with core 1 based O-glycans, and the other exclusively containing Tn/STn structures. Importantly, Tn antigen present on IgA1 from IgAN patients and controls was convertible into the core 1 structure in vitro by recombinant T-synthase. Our results demonstrate that undergalactosylation of O-glycans in IgA1 is not restricted to IgAN and suggest that in vivo inefficiency of T-synthase toward IgA1 in a subpopulation of B or plasma cells, as well as overall elevation of IgA, may contribute to IgAN pathogenesis.

Indexed as

AdultAntigens, Tumor-Associated, CarbohydrateB-LymphocytesFemaleGalactoseGalactosyltransferasesGlomerular MesangiumGlomerulonephritis, IGAGlycosylationHumansImmunoglobulin AInflammationLectinsMalePeanut AgglutininPolysaccharidesAntigens, Tumor-Associated, CarbohydrateC1GALT1 protein, humanGalactosegalactosyl-1-3-N-acetylgalactosaminyl-specific 2,6-sialyltransferaseGalactosyltransferasesHelix lectinImmunoglobulin ALectinsPeanut AgglutininPolysaccharidesSialyltransferasesTn antigen

Identifiers

PMID25071157
PMCPMC4223494
OpenAlexW2087471889

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.