Evidence map›Paper›PMID 23169140›Full record

ArticleEuropean journal of immunology2013

IL-21 promotes the production of anti-DNA IgG but is dispensable for kidney damage in lyn-/- mice.

Toni Gutierrez, Jessica M Mayeux, Sterling B Ortega, Nitin J Karandikar, Quan-Zhen Li, Dinesh Rakheja, Xin J Zhou, Anne B Satterthwaite

Open access · bronzeAbstract read
In one paragraph

Article in European journal of immunology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. The Heterogeneity of Breast Cancer Metabolism.Advances in experimental medicine and biology · 2021
    Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Breast Cancer Metabolism.Advances in experimental medicine and biology
    Review
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

8 authors at 2 institutions in 1 country.

Toni GutierrezDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390-8884, USA.
Jessica M Mayeux
Sterling B Ortega
Nitin J Karandikar
Quan-Zhen Li
Dinesh Rakheja
Xin J Zhou
Anne B Satterthwaite
The University of Texas Southwestern Medical Center · USBaylor University Medical Center · US

Funding

Sle triggered disease pathwaysP01AI039824 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI WAKELAND, EDWARD K. · 1996 to 2011
$13.0M
SLAM Genes-from Mouse to ManP50AR055503 · NIAMS · UT SOUTHWESTERN MEDICAL CENTER · PI KARP, DAVID R · 2007 to 2011
$8.3M
DISSECTING THE IMMUNE BASIS OF DISEASE AND THERAPYK24AI079272 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI KARANDIKAR, NITIN J · 2009 to 2013
$1.1M
Role of Hyperresponsive Myeloid Cells in Murine LupusF31GM076982 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI GUTIERREZ, MARIA A · 2006 to 2010
$148k
NIAID NIH HHS K24 AI079272NIAID NIH HHS K24AI079272NIAID NIH HHS P01 AI039824NIAMS NIH HHS NIH P50 AR055503NIAMS NIH HHS P50 AR055503NIGMS NIH HHS 1 F31 GM076982NIGMS NIH HHS F31 GM076982
6 · The paper itself

Abstract

The autoimmune disease systemic lupus erythematosus is characterized by loss of tolerance to nuclear Ags and a heightened inflammatory environment, which together result in end organ damage. Lyn-deficient mice, a model of systemic lupus erythematosus, lack an inhibitor of B-cell and myeloid cell activation. This results in B-cell hyper-responsiveness, plasma cell accumulation, autoantibodies, and glomerulonephritis (GN). IL-21 is associated with autoimmunity in mice and humans and promotes B-cell differentiation and class switching. Here, we explore the role of IL-21 in the autoimmune phenotypes of lyn(-/-) mice. We find that IL-21 mRNA is reduced in the spleens of lyn(-/-) IL-6(-/-) and lyn(-/-) Btk(lo) mice, neither of which produce pathogenic autoantibodies or develop significant GN. While IL-21 is dispensable for plasma cell accumulation and IgM autoantibodies in lyn(-/-) mice, it is required for anti-DNA IgG antibodies and some aspects of T-cell activation. Surprisingly, GN still develops in lyn(-/-) IL-21(-/-) mice. This likely results from the presence of IgG autoantibodies against a limited set of non-DNA Ags. These studies identify a specific role for IL-21 in the class switching of anti-DNA B cells and demonstrate that neither IL-21 nor anti-DNA IgG is required for kidney damage in lyn(-/-) mice.

Indexed as

Agammaglobulinaemia Tyrosine KinaseAnimalsAntibodies, AntinuclearAutoantibodiesAutoimmune DiseasesB-LymphocytesDNAGlomerulonephritisImmunoglobulin GInterleukin-21Interleukin-6InterleukinsKidneyLupus Erythematosus, SystemicLymphocyte ActivationMiceAgammaglobulinaemia Tyrosine KinaseAntibodies, AntinuclearAutoantibodiesBTK protein, humanDNAImmunoglobulin GInterleukin-21Interleukin-6Interleukinslyn protein-tyrosine kinaseProtein-Tyrosine Kinasessrc-Family Kinases

Identifiers

PMID23169140
PMCPMC3768150
OpenAlexW1906753042

What OpenQuestion holds

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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.