Evidence map›Paper›PMID 26070934›Full record

ReviewCytokine2015

IL-4 and IL-13 signaling in allergic airway disease.

Naina Gour, Marsha Wills-Karp

Abstract readReview
In one paragraph

Review in Cytokine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 249 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
249citing papers in PubMed, 4 pooled it
–field-weighted citation impact
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

249 citing papers in PubMed, 4 syntheses or guidelines pooled it.

  1. Real-world efficacy of treatment with benralizumab, dupilumab, mepolizumab and reslizumab for severe asthma: A systematic review and meta-analysis.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2022
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  15. Engineering Chimeric Hypoallergens for Safer and More Effective House Dust Mite Allergy Vaccines.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2026
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189 more citing papers are in PubMed but not listed here.

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

2 authors.

Naina GourDepartment of Environmental Health Sciences, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States.
Marsha Wills-KarpDepartment of Environmental Health Sciences, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States. Electronic address: mwkarp@jhu.edu.

Funding

TSLP, IL-9-producing mucosal mast cells, and allergic inflammationU19AI070235 · NIAID · CINCINNATI CHILDRENS HOSP MED CTR · PI Marc E. Rothenberg · 2006 to 2026
$31.3M
Traning Program in Environmental Health SciencesT32ES007141 · NIEHS · JOHNS HOPKINS UNIVERSITY · PI Marsha Wills-Karp · 1985 to 2026
$22.2M
Epithelial Regulation of Th2 Immune Responses in the LungR01AI083315 · NIAID · JOHNS HOPKINS UNIVERSITY · PI WILLS-KARP, MARSHA · 2009 to 2013
$1.9M
NIAID NIH HHS R01 AI083315NIAID NIH HHS R01AI083315NIAID NIH HHS U19 AI070235NIAID NIH HHS U19AI070235NIEHS NIH HHS NIEHST32ES007141NIEHS NIH HHS T32 ES007141
6 · The paper itself

Abstract

Aberrant production of the prototypical type 2 cytokines, interleukin (IL)-4 and IL-13 has long been associated with the pathogenesis of allergic disorders. Despite tremendous scientific inquiry, the similarities in their structure, and receptor usage have made it difficult to ascertain the distinct role that these two look-alike cytokines play in the onset and perpetuation of allergic inflammation. However, recent discoveries of differences in receptor distribution, utilization/assembly and affinity between IL-4 and IL-13, along with the discovery of unique innate lymphoid 2 cells (ILC2) which preferentially produce IL-13, not IL-4, are beginning to shed light on these mysteries. The purpose of this chapter is to review our current understanding of the distinct roles that IL-4 and IL-13 play in allergic inflammatory states and the utility of their modulation as potential therapeutic strategies for the treatment of allergic disorders.

Indexed as

AnimalsAsthmaClinical Trials as TopicCytokinesDisease Models, AnimalEpithelial CellsFibrosisHumansHypersensitivityImmunity, InnateInflammationInterleukin-13Interleukin-4LymphocytesMacrophagesMiceCytokinesIL13 protein, humanIL4 protein, humanInterleukin-13Interleukin-4AllergyAsthmaIL-13IL-4

Identifiers

PMID26070934
PMCPMC4532591

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.