Evidence map›Paper›PMID 24740503›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2014

Protection from intestinal inflammation by bacterial exopolysaccharides.

Sara E Jones, Mallory L Paynich, Daniel B Kearns, Katherine L Knight

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

47 citing papers in PubMed, 107 citations in OpenAlex.

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  15. Defining Early Steps inbioRxiv : the preprint server for biology · 2023
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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

4 authors at 2 institutions in 1 country.

Sara E JonesDepartment of Microbiology and Immunology, Loyola University Chicago, Maywood, IL 60153.
Mallory L Paynich
Daniel B Kearns
Katherine L Knight
Loyola University Chicago · USIndiana University Bloomington · US

Funding

Somatic Diversification of Immunoglobulin Genes in GALTR01AI050260 · NIAID · LOYOLA UNIVERSITY CHICAGO · PI KNIGHT, KATHERINE L. · 2001 to 2015
$5.1M
Experimental Immunology Training GrantT32AI007508 · NIAID · LOYOLA UNIVERSITY CHICAGO · PI KNIGHT, KATHERINE L. · 1997 to 2022
$4.0M
Protection from enteric pathogens by beneficial microbesR21AI098187 · NIAID · LOYOLA UNIVERSITY CHICAGO · PI KNIGHT, KATHERINE L. · 2012 to 2013
$401k
B. subtilis Reduces Intestinal Inflammation via TLR Signaling and B1 LymphocytesF32DK092054 · NIDDK · LOYOLA UNIVERSITY CHICAGO · PI JONES, SARA ELIZABETH · 2011 to 2012
$105k
NIAID NIH HHS R01 AI050260NIAID NIH HHS R21 AI 098187NIAID NIH HHS R21 AI098187NIAID NIH HHS T32 AI007508NIDDK NIH HHS F32 DK092054NIDDK NIH HHS F32 DK 92054
6 · The paper itself

Abstract

Host inflammatory responses against pathogenic organisms can be abrogated by commensals; however, the molecular mechanisms by which pathogenesis is prevented are still poorly understood. Previous studies demonstrated that administration of a single dose of Bacillus subtilis prevented disease and inflammation by the enteric mouse pathogen Citrobacter rodentium, which causes disease similar to the human pathogen enteropathogenic Escherichia coli. No protection was observed when an exopolysaccharide (EPS)-deficient mutant of B. subtilis was used, suggesting that EPS are the protective factor. In this study, we isolated and characterized EPS and showed that they also prevent C. rodentium-associated intestinal disease after a single injection. Protection is TLR4 dependent because EPS-treated TLR4 knockout mice developed disease. Furthermore, protection could be conveyed to wild-type mice by adoptive transfer of macrophage-rich peritoneal cells from EPS-treated mice. We found that EPS specifically bind peritoneal macrophages, and because mice lacking MyD88 signaling in myeloid cells were not protected by EPS, we conclude that bacterial EPS prevent colitis in a TLR4-dependent manner that requires myeloid cells. These studies provide a simple means of preventing intestinal inflammation caused by enteric pathogens.

Indexed as

AnimalsBacteriaHumansInflammationIntestinesMacrophages, PeritonealMiceMice, KnockoutMyeloid Differentiation Factor 88Polysaccharides, BacterialToll-Like Receptor 4Myd88 protein, mouseMyeloid Differentiation Factor 88Polysaccharides, BacterialTlr4 protein, mouseToll-Like Receptor 4

Identifiers

PMID24740503
PMCPMC4018721
OpenAlexW1505421911

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.