Evidence map›Paper›PMID 27245920›Full record

ArticleBMC immunology2016

Eosinophils may play regionally disparate roles in influencing IgA(+) plasma cell numbers during large and small intestinal inflammation.

Ruth Forman, Michael Bramhall, Larisa Logunova, Marcus Svensson-Frej, Sheena M Cruickshank, Kathryn J Else

Open access · goldAbstract read
In one paragraph

Article in BMC immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

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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

6 authors at 2 institutions in 2 countries.

Ruth FormanDepartment of Immunology, University of Manchester, Manchester, UK. ruth.forman@manchester.ac.uk.
Michael BramhallDepartment of Immunology, University of Manchester, Manchester, UK.
Larisa LogunovaDepartment of Immunology, University of Manchester, Manchester, UK.
Marcus Svensson-FrejImmunology section, Lund University, BMC D14, Lund, SE-22184, Sweden.
Sheena M CruickshankDepartment of Immunology, University of Manchester, Manchester, UK.
Kathryn J ElseDepartment of Immunology, University of Manchester, Manchester, UK.
University of Manchester · GBLund University · SE

Funding

Biotechnology and Biological Sciences Research CouncilWellcome TrustWellcome Trust 092323
6 · The paper itself

Abstract

backgroundEosinophils are innate immune cells present in the intestine during steady state conditions. An intestinal eosinophilia is a hallmark of many infections and an accumulation of eosinophils is also observed in the intestine during inflammatory disorders. Classically the function of eosinophils has been associated with tissue destruction, due to the release of cytotoxic granule contents. However, recent evidence has demonstrated that the eosinophil plays a more diverse role in the immune system than previously acknowledged, including shaping adaptive immune responses and providing plasma cell survival factors during the steady state. Importantly, it is known that there are regional differences in the underlying immunology of the small and large intestine, but whether there are differences in context of the intestinal eosinophil in the steady state or inflammation is not known.

resultsOur data demonstrates that there are fewer IgA(+) plasma cells in the small intestine of eosinophil-deficient ΔdblGATA-1 mice compared to eosinophil-sufficient wild-type mice, with the difference becoming significant post-infection with Toxoplasma gondii. Remarkably, and in complete contrast, the absence of eosinophils in the inflamed large intestine does not impact on IgA(+) cell numbers during steady state, and is associated with a significant increase in IgA(+) cells post-infection with Trichuris muris compared to wild-type mice. Thus, the intestinal eosinophil appears to be less important in sustaining the IgA(+) cell pool in the large intestine compared to the small intestine, and in fact, our data suggests eosinophils play an inhibitory role. The dichotomy in the influence of the eosinophil over small and large intestinal IgA(+) cells did not depend on differences in plasma cell growth factors, recruitment potential or proliferation within the different regions of the gastrointestinal tract (GIT).

conclusionsWe demonstrate for the first time that there are regional differences in the requirement of eosinophils for maintaining IgA+ cells between the large and small intestine, which are more pronounced during inflammation. This is an important step towards further delineation of the enigmatic functions of gut-resident eosinophils.

Indexed as

AnimalsCells, CulturedCellular MicroenvironmentEosinophilsGATA1 Transcription FactorImmunoglobulin AInflammationIntestine, LargeIntestine, SmallMaleMiceMice, Inbred BALB CMice, KnockoutPlasma CellsToxoplasmaToxoplasmosis, AnimalGata1 protein, mouseGATA1 Transcription FactorImmunoglobulin AB cellEosinophilInflammationIntestinalPlasma cellRegionToxoplasmaTrichuris

Identifiers

PMID27245920
PMCPMC4886441
OpenAlexW2412785742

What OpenQuestion holds

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LicenceCC BY
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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.