Evidence map›Paper›PMID 20018622›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2010

Differential regulation of IL-4Ralpha expression by antigen versus cytokine stimulation characterizes Th2 progression in vivo.

Georgia Perona-Wright, Katja Mohrs, Katrin D Mayer, Markus Mohrs

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

21 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Expression Efficiency of MultipleImmunoHorizons · 2020
    Article
  6. IL-4 controls activated neutrophil FcγR2b expression and migration into inflamed joints.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  7. Article
  8. Review
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  19. Influence of endogenous opioid systems on T lymphocytes as assessed by the knockout of mu, delta and kappa opioid receptors.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2011
    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

4 authors at 1 institution in 1 country.

Georgia Perona-WrightTrudeau Institute, Saranac Lake, NY 12983, USA.
Katja Mohrs
Katrin D Mayer
Markus Mohrs
Trudeau Institute · US

Funding

The interdependence between T and B cells in Th2 cell differentiationR01AI076479 · NIAID · TRUDEAU INSTITUTE, INC. · PI MOHRS, MARKUS · 2008 to 2012
$2.0M
The role of IL-4 and IL-4Ralpha in the multi-step process of Th2 developmentR01AI072296 · NIAID · TRUDEAU INSTITUTE, INC. · PI MOHRS, MARKUS · 2007 to 2011
$2.0M
NIAID NIH HHS AI072296NIAID NIH HHS AI076479NIAID NIH HHS R01 AI072296NIAID NIH HHS R01 AI076479
6 · The paper itself

Abstract

IL-4 promotes Th2 differentiation and provides immunity to helminth infections but is also associated with allergy and asthma. This suggests that precise adjustment of IL-4 responsiveness is needed to correctly balance immune responses. The IL-4Ralpha chain is an essential component of the IL-4 receptor and signals via STAT6. In this study, we show that infection with a helminth pathogen elicited broad upregulation of IL-4Ralpha on bystander CD4+ T cells in the draining lymph node, while simultaneously resulting in the loss of IL-4Ralpha expression on activated Th2 cells. IL-4Ralpha upregulation was restricted to the reactive lymph node, occurred within 4 d of infection, and was driven by an IL-4- and STAT6-dependent mechanism. Mice heterozygous for Stat6 exhibited reduced IL-4Ralpha upregulation and a correspondingly attenuated Th2 response. Indeed, the enhanced IL-4Ralpha upregulation in BALB/c mice, compared with that in C57BL6 mice, predicted their stronger Th2 response. The selective downregulation of IL-4Ralpha on highly activated Th cells was triggered by antigenic stimulation, was accompanied by loss of IL-7Ralpha, and rendered the cells unresponsive to IL-4. Together these data reveal a tightly controlled program of changing IL-4 responsiveness that characterizes the initiation, amplification, and restriction of a Th2 response in vivo.

Indexed as

AnimalsAntigensBystander EffectCell DifferentiationCytokinesGene Expression RegulationHelminthsInterleukin-4Interleukin-4 Receptor alpha SubunitLymph NodesMiceMice, Inbred BALB CMice, Inbred C57BLSTAT6 Transcription FactorTh2 CellsAntigensCytokinesInterleukin-4Interleukin-4 Receptor alpha SubunitStat6 protein, mouseSTAT6 Transcription Factor

Identifiers

PMID20018622
PMCPMC3066071
OpenAlexW1894404946

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.