Evidence map›Paper›PMID 24084078›Full record

ReviewThe Journal of allergy and clinical immunology2014

A molecular perspective on TH2-promoting cytokine receptors in patients with allergic disease.

Martin J Romeo, Rachana Agrawal, Anna Pomés, Judith A Woodfolk

Open access · bronzeAbstract readReview
In one paragraph

Review in The Journal of allergy and clinical immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
3.0field-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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 50 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Modulation of IL-4/IL-13 cytokine signaling in the context of allergic disease.The Journal of allergy and clinical immunology · 2022
    Review
  5. Interleukin-5 receptor alpha (CD125) expression on human blood and lung neutrophils.Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology · 2022
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. TThe Journal of allergy and clinical immunology · 2018
    Article
  12. Article
  13. Pathogenic CD4The Journal of allergy and clinical immunology · 2017
    Review
  14. Review
  15. Article
  16. Reply: To PMID 24084078.The Journal of allergy and clinical immunology · 2014
    Article
  17. Article
  18. Article
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  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Martin J RomeoAsthma and Allergic Diseases Center, University of Virginia, Charlottesville, Va.
Rachana AgrawalAsthma and Allergic Diseases Center, University of Virginia, Charlottesville, Va.
Anna PomésIndoor Biotechnologies Inc, Charlottesville, Va.
Judith A WoodfolkAsthma and Allergic Diseases Center, University of Virginia, Charlottesville, Va. Electronic address: jaw4m@virginia.edu.
University of Virginia · USIndoor Biotechnologies (United States) · US

Funding

Immune Response to Cat: Regulatory and Effector T CellsR01AI052196 · NIAID · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI WOODFOLK, JUDITH A · 2004 to 2013
$2.9M
Regulation of TSLP receptor expression and function in eczema in mice and manR01AR059058 · NIAMS · UNIVERSITY OF VIRGINIA · PI WOODFOLK, JUDITH A, ZIEGLER, STEVEN F · 2011 to 2015
$2.7M
NIAID NIH HHS R01 AI-052196NIAID NIH HHS R01 AI052196NIAMS NIH HHS R01 AR-059058NIAMS NIH HHS R01 AR059058
6 · The paper itself

Abstract

The cytokines IL-4, IL-13, and thymic stromal lymphopoietin play a key role in allergic disease by virtue of their ability to initiate, maintain, and augment TH2 responses. These molecules mediate their effects through type 1 cytokine receptors, which bind cytokines with a characteristic structure. Receptors are expressed on a broad array of immune cell types and are integral to complex cytokine networks operating in health and disease. TH2-promoting cytokines bind different configurations of receptors. Receptor subunits can exist in surface-bound or soluble forms, as well as in isolation or in partnership with other subunits. Sharing of receptor subunits among different cytokine receptor complexes adds to the intricate landscape. This article describes the characteristics of receptors for IL-4, IL-13, and thymic stromal lymphopoietin and their respective ligands from a structure-function perspective. We detail the mechanisms of receptor complex assembly, the interrelated nature of these receptors, and the effect on allergic inflammation. The ability for novel and atypical types of receptors to modulate inflammatory processes is also discussed. We highlight current and emerging treatments that target TH2-promoting receptor complexes. Understanding the molecular features of these receptors provides insight into different disease phenotypes and the variable clinical outcomes arising from targeted therapies. These considerations can be used to inform future directions for research and creative strategies for treating individual patients.

Indexed as

AnimalsCytokinesHumansHypersensitivityProtein BindingProtein Interaction MapsReceptors, CytokineSignal TransductionTh2 CellsCytokinesReceptors, Cytokineallergyasthma treatmentcytokinesIL-13IL-4receptorsT(H)2Thymic stromal lymphopoietin

Identifiers

PMID24084078
PMCPMC3969406
OpenAlexW2152767905

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.