Evidence map›Paper›PMID 25010390›Full record

ArticleCytokine2014

Aberrant production of IL-13 by T cells promotes exocrinopathy in Id3 knockout mice.

Ian Belle, Josh Mahlios, Andrew McKenzie, Yuan Zhuang

Open access · greenAbstract read
In one paragraph

Article in Cytokine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

6 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Review
  3. Id3 Restricts γδ NKT Cell Expansion by Controlling Egr2 and c-Myc Activity.Journal of immunology (Baltimore, Md. : 1950) · 2018
    Article
  4. Article
  5. Article
  6. Id2 Collaborates with Id3 To Suppress Invariant NKT and Innate-like Tumors.Journal of immunology (Baltimore, Md. : 1950) · 2017
    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

4 authors at 3 institutions in 2 countries.

Ian BelleDepartment of Immunology, Duke University Medical Center, Durham, NC 27710, USA.
Josh MahliosDepartment of Immunology, Duke University Medical Center, Durham, NC 27710, USA.
Andrew McKenzieMRC Laboratory of Molecular Biology, Cambridge CB2 0QH, UK.
Yuan ZhuangDepartment of Immunology, Duke University Medical Center, Durham, NC 27710, USA. Electronic address: yzhuang@duke.edu.
Duke Medical Center · USDuke University · USMRC Laboratory of Molecular Biology · GB

Funding

HEB MEDIATED PATHWAYS AND FUNCTION IN T CELL DEVELOPMENTR01GM059638 · NIGMS · DUKE UNIVERSITY · PI CHAN, FRANCIS KAMING · 1999 to 2021
$6.9M
Basic Immunology Training ProgramT32AI052077 · NIAID · DUKE UNIVERSITY · PI KRANGEL, MICHAEL S · 2002 to 2024
$4.2M
Medical Research Council MC_U105178805NIAID NIH HHS T32 AI052077NIGMS NIH HHS GM059638NIGMS NIH HHS R01 GM059638
6 · The paper itself

Abstract

Elevated levels of the cytokine IL-13 has been found to be associated with autoimmune diseases, including Sjögren's Syndrome. However, whether IL-13 plays a causative role in disease development is not known and cannot be easily studied in humans. Our previous work has shown that levels of IL-13 are elevated in Id3 knockout mice, which has been established as a model for primary Sjögren's Syndrome. Here, we utilized an IL-13 reporter to determine the source of the elevated IL-13 levels observed in Id3 knockout mice and assess its contribution to SS pathology. Our results indicate that T cells, notably CD4 and γδ T cells, in Id3 knockout mice acquire IL-13 competency at an elevated rate well before disease symptoms become apparent. We also show that T cells developing early in life are more predisposed to produce IL-13. Finally, analysis of Id3 and IL-13 double deficient mice demonstrated that IL-13 plays an essential role in the deterioration of gland function. Our study provides crucial genetic evidence that enhanced IL-13 production by T cells can play a causative role in the exocrinopathy observed in Id3 knockout mice.

Indexed as

AgingAnimalsAnimals, NewbornExocrine GlandsInhibitor of Differentiation ProteinsInterleukin-13Mice, KnockoutReceptors, Antigen, T-Cell, gamma-deltaSalivary GlandsThymocytesT-LymphocytesIdb3 protein, mouseInhibitor of Differentiation ProteinsInterleukin-13Receptors, Antigen, T-Cell, gamma-deltaCD4 T cellsId3IL-13Sjögren’s Syndromeγδ T cells

Identifiers

PMID25010390
PMCPMC4127355
OpenAlexW2093218571

What OpenQuestion holds

Textmetadata
LicenceTDM
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.