Evidence map›Paper›PMID 26825533›Full record

ArticleJournal of the American Society of Nephrology : JASN2016

IgA Structure Variations Associate with Immune Stimulations and IgA Mesangial Deposition.

Zeliha Oruc, Christelle Oblet, Ahmed Boumediene, Anne Druilhe, Virginie Pascal, Elisabeth Le Rumeur, Armelle Cuvillier, Chahrazed El Hamel, Sandrine Lecardeur, Tomas Leanderson and 4 more

Abstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Are there animal models of IgA nephropathy?Seminars in immunopathology · 2021
    Review
  8. Review
  9. History of IgA Nephropathy Mouse Models.Journal of clinical medicine · 2021
    Review
  10. Article
  11. Aberrant mucosal immunoreaction to tonsillar microbiota in immunoglobulin A nephropathy.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2021
    Article
  12. Article
  13. Article
  14. Article
  15. 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 at 4 institutions in 3 countries.

Zeliha OrucLimoges University Hospital Dupuytren, Centre National de la Recherche Scientifique, Limoges University, Limoges, France;
Christelle ObletLimoges University Hospital Dupuytren, Centre National de la Recherche Scientifique, Limoges University, Limoges, France;
Ahmed BoumedieneLimoges University Hospital Dupuytren, Centre National de la Recherche Scientifique, Limoges University, Limoges, France;
Anne DruilheLimoges University Hospital Dupuytren, Centre National de la Recherche Scientifique, Limoges University, Limoges, France;
Virginie PascalLimoges University Hospital Dupuytren, Centre National de la Recherche Scientifique, Limoges University, Limoges, France;
Elisabeth Le RumeurGenetics and Development Instittute, Rennes University, Centre National de la Recherche Scientifique, Rennes, France;
Armelle CuvillierB Cell Design, Limoges, France;
Chahrazed El HamelLimoges University Hospital Dupuytren, Centre National de la Recherche Scientifique, Limoges University, Limoges, France;
Sandrine LecardeurLimoges University Hospital Dupuytren, Centre National de la Recherche Scientifique, Limoges University, Limoges, France;
Tomas LeandersonImmunology Group, Lund University, Lund, Sweden;
Willy MorelleCentre National de la Recherche Scientifique, Laboratory of Structural and Functional Glycobiology, University of Lille 1, France; and.
Jocelyne DemengeotInstituto Gulbenkian de Ciência, Oeiras, Portugal.
Jean-Claude AldigierLimoges University Hospital Dupuytren, Centre National de la Recherche Scientifique, Limoges University, Limoges, France;
Michel CognéLimoges University Hospital Dupuytren, Centre National de la Recherche Scientifique, Limoges University, Limoges, France; cogne@unilim.fr.
Institut de génétique et de développement de Rennes · FRInstituto Gulbenkian de Ciência · PTLund University · SEUniversité de Lille · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IgA1 mesangial deposition is the hallmark of IgA nephropathy and Henoch-Schönlein purpura, the onset of which often follows infections. Deposited IgA has been reported as polymeric, J chain associated, and often, hypogalactosylated but with no information concerning the influence of the IgA repertoire or the link between immune stimuli and IgA structure. We explored these issues in the α1KI mouse model, which produces polyclonal human IgA1 prone to mesangial deposition. Compared with mice challenged by a conventional environment, mice in a specific pathogen-free environment had less IgA deposition. However, serum IgA of specific pathogen-free mice showed more galactosylation and much lower polymerization. Notably, wild-type, α1KI, and even J chain-deficient mice showed increased polymeric serum IgA on exposure to pathogens. Strict germfree conditions delayed but did not completely prevent deposition; mice housed in these conditions had very low serum IgA levels and produced essentially monomeric IgA. Finally, comparing monoclonal IgA1 that had different variable regions and mesangial deposition patterns indicated that, independently of glycosylation and polymerization, deposition might also depend on IgA carrying specific variable domains. Together with IgA quantities and constant region post-translational modifications, repertoire changes during immune responses might, thus, modulate IgA propensity to deposition. These IgA features are not associated with circulating immune complexes and C3 deposition and are more pertinent to an initial IgA deposition step preceding overt clinical symptoms in patients.

Indexed as

AnimalsAntibody FormationFemaleGlomerular MesangiumImmunoglobulin AMaleMiceProtein ConformationImmunoglobulin AIgAIgA depositionIgA nephropathyImmunology and pathologytransgenic mouse

Identifiers

PMID26825533
PMCPMC5004660
OpenAlexW2255525318

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.