Evidence map›Paper›PMID 26131743›Full record

ArticleKidney international2015

IL-3 contributes to development of lupus nephritis in MRL/lpr mice.

Kerstin Renner, Fabian Johannes Hermann, Kathrin Schmidbauer, Yvonne Talke, Manuel Rodriguez Gomez, Gabriela Schiechl, Jens Schlossmann, Hilke Brühl, Hans-Joachim Anders, Matthias Mack

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Kidney international, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.2field-weighted citation impact, top 9% 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

29 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
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  6. Article
  7. Roles of Cytokines in Alzheimer's Disease.International journal of molecular sciences · 2024
    Review
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  10. IL-3: key orchestrator of inflammation.Frontiers in immunology · 2024
    Review
  11. mSphere · 2023
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Generation of IL-3-Secreting CD4ImmunoHorizons · 2019
    Article
  19. Innate Immune Modulation by GM-CSF and IL-3 in Health and Disease.International journal of molecular sciences · 2019
    Review
  20. Self-reactive CD4The Journal of experimental medicine · 2019
    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

10 authors at 3 institutions in 1 country.

Kerstin RennerDepartment of Internal Medicine II, University Hospital Regensburg, Regensburg, Germany.
Fabian Johannes HermannDepartment of Internal Medicine II, University Hospital Regensburg, Regensburg, Germany.
Kathrin SchmidbauerDepartment of Internal Medicine II, University Hospital Regensburg, Regensburg, Germany.
Yvonne TalkeDepartment of Internal Medicine II, University Hospital Regensburg, Regensburg, Germany.
Manuel Rodriguez GomezDepartment of Internal Medicine II, University Hospital Regensburg, Regensburg, Germany.
Gabriela SchiechlDepartment of Internal Medicine II, University Hospital Regensburg, Regensburg, Germany.
Jens SchlossmannDepartment of Pharmacology and Toxicology, University Regensburg, Regensburg, Germany.
Hilke BrühlDepartment of Internal Medicine I, University Hospital Regensburg, Regensburg, Germany.
Hans-Joachim AndersMedizinische Klinik and Poliklinik IV, Klinikum der LMU München, München, Germany.
Matthias MackDepartment of Internal Medicine II, University Hospital Regensburg, Regensburg, Germany.
University Hospital Regensburg · DELMU Klinikum · DEUniversity of Regensburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MRL/lpr mice develop a spontaneous autoimmune disease that closely resembles human systemic lupus erythematosus (SLE) with DNA autoantibodies, hypergammaglobulinemia, immune complex glomerulonephritis, and systemic vasculitis. Little is known about the role of IL-3 in SLE. In order to study this we analyzed the expression of IL-3 in murine lupus and determined whether blockade of IL-3 with a monoclonal antibody or injection of recombinant IL-3 affects lupus nephritis in MRL/lpr mice. During disease progression IL-3 levels were increased in the plasma and in the supernatant of cultured splenocytes from MRL/lpr mice. Administration of IL-3 aggravated the disease with significantly higher renal activity scores, more renal fibrosis, and more glomerular leukocyte infiltration and IgG deposition. Blockade of IL-3 significantly improved acute and chronic kidney damage, reduced the glomerular infiltration of leukocytes and the glomerular deposition of IgG, and decreased the development of renal fibrosis. Furthermore, DNA autoantibody production, proteinuria, and serum creatinine levels were significantly lower in the anti-IL-3 group. Thus, IL-3 plays an important role in the pathogenesis of SLE and the progression of lupus nephritis. Hence, blockade of IL-3 may represent a new strategy for treatment of lupus nephritis.

Indexed as

AnimalsAntibodiesAntibodies, AntinuclearCells, CulturedCreatinineDisease ProgressionFibrosisImmunoglobulin GInterleukin-3Kidney GlomerulusLupus NephritisLymphocyte CountMiceProteinuriaSeverity of Illness IndexSpleenAntibodiesAntibodies, AntinuclearCreatinineImmunoglobulin GInterleukin-3

Identifiers

PMID26131743
OpenAlexW1595393546

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.