Evidence map›Paper›PMID 23839064›Full record

ArticleMucosal immunology2014

IKKβ in intestinal epithelial cells regulates allergen-specific IgA and allergic inflammation at distant mucosal sites.

A Bonnegarde-Bernard, J Jee, M J Fial, F Aeffner, E Cormet-Boyaka, I C Davis, M Lin, D Tomé, M Karin, Y Sun and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Mucosal immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Inhibition of elastase enhances the adjuvanticity of alum and promotes anti-SARS-CoV-2 systemic and mucosal immunity.Proceedings of the National Academy of Sciences of the United States of America · 2021
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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

11 authors at 4 institutions in 2 countries.

A Bonnegarde-Bernard1] Department of Veterinary Biosciences, The Ohio State University, Columbus, Ohio, USA [2] Laboratory of Human Nutrition, Agro Paris Tech, Paris, France.
J JeeDepartment of Veterinary Biosciences, The Ohio State University, Columbus, Ohio, USA.
M J FialDepartment of Veterinary Biosciences, The Ohio State University, Columbus, Ohio, USA.
F AeffnerDepartment of Veterinary Biosciences, The Ohio State University, Columbus, Ohio, USA.
E Cormet-BoyakaDepartment of Internal Medicine, The Ohio State University, Columbus, Ohio, USA.
I C DavisDepartment of Veterinary Biosciences, The Ohio State University, Columbus, Ohio, USA.
M LinDepartment of Veterinary Biosciences, The Ohio State University, Columbus, Ohio, USA.
D ToméLaboratory of Human Nutrition, Agro Paris Tech, Paris, France.
M KarinDepartment of Pharmacology, University of California, La Jolla, California, USA.
Y SunResearch and Testing Laboratory, Lubbock, Texas, USA.
P N Boyaka1] Department of Veterinary Biosciences, The Ohio State University, Columbus, Ohio, USA [2] Department of Internal Medicine, The Ohio State University, Columbus, Ohio, USA.
The Ohio State University · USArkansas Agricultural Experiment Station · USParisTech · FRUniversity of California, San Diego · US

Funding

MOLECULAR ADJUVANTS FOR NALT-BASED IMMUNITY TO ANTHRAXR01AI043197 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BOYAKA, PROSPER N · 1998 to 2013
$4.6M
NIAID NIH HHS R01 AI043197
6 · The paper itself

Abstract

Regulation of allergic responses by intestinal epithelial cells (IECs) remains poorly understood. Using a model of oral allergen sensitization in the presence of cholera toxin as adjuvant and mice with cell-specific deletion of inhibitor-κB kinase (IKKβ) in IECs (IKKβ(ΔIEC)), we addressed the contribution of IECs to allergic sensitization to ingested antigens and allergic manifestations at distant mucosal site of the airways. Cholera toxin induced higher pro-inflammatory responses and altered the profile of the gut microbiota in IKKβ(ΔIEC) mice. Antigen-specific immunoglobulin E (IgE) responses were unaltered in IKKβ(ΔIEC) mice, but their IgA antibodies (Abs), T helper type 1 (Th1) and Th17 responses were enhanced. Upon nasal antigen challenge, these mice developed lower levels of allergic lung inflammation, which correlated with higher levels of IgA Abs in the airways. The IKKβ(ΔIEC) mice also recruited a higher number of gut-sensitized T cells in the airways after nasal antigen challenge and developed airway hyper-responsiveness, which were suppressed by treatment with anti-interleukin-17A. Fecal microbiota transplant during allergic sensitization reduced Th17 responses in IKKβ(ΔIEC) mice, but did not affect IgA Ab responses. In summary, we show that IKKβ in IECs shapes the gut microbiota and immune responses to ingested antigens and influences allergic responses in the airways via regulation of IgA Ab responses.

Indexed as

Adjuvants, ImmunologicAllergensAnimalsAntibody SpecificityCD4-Positive T-LymphocytesCholera ToxinDysbiosisGene DeletionI-kappa B KinaseImmunity, InnateImmunizationImmunoglobulin AInflammationInterleukin-17Intestinal MucosaMiceAdjuvants, ImmunologicAllergensCholera ToxinI-kappa B KinaseImmunoglobulin AInterleukin-17

Identifiers

PMID23839064
PMCPMC4053573
OpenAlexW2010220237

What OpenQuestion holds

Textmetadata
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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.