Evidence map›Paper›PMID 14684582›Full record

ArticleGut2004

Systemic antibodies towards mucosal bacteria in ulcerative colitis and Crohn's disease differentially activate the innate immune response.

E Furrie, S Macfarlane, J H Cummings, G T Macfarlane

2 registry-linked trialsOpen access · bronzeAbstract read
In one paragraph

Article in Gut, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
2.6field-weighted citation impact, top 10% 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.

NCT00305409 nacompletednot on this mapstarted 2006, after this paper: background citation

Synbiotic Treatment in Crohn's Disease Patients

TypeinterventionalSponsorUniversity of DundeeRan2006 to 2008Enrolled50ConditionsCrohn's DiseaseArmsSynbiotic (Synergy I / B.longum)
NCT00803829 nacompletednot on this mapstarted 2009, after this paper: background citation

Synbiotic Treatment of Ulcerative Colitis Patients

TypeinterventionalSponsorUniversity of DundeeRan2009 to 2011Enrolled24ConditionsUlcerative ColitisArmsSynbiotic (Synergy1/B. longum)
3 · Its place in the literature

Who cites it

43 citing papers in PubMed, 86 citations in OpenAlex.

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  15. Pathogenicity of Enterococci.Microbiology spectrum · 2019
    Review
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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.

E FurrieMRC Microbiology and Gut Biology Group, University of Dundee, Ninewells Hospital and Medical School, Dundee, UK. e.furrie@dundee.ac.uk
S Macfarlane
J H Cummings
G T Macfarlane
Ninewells Hospital · GBUniversity of Dundee · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsThe mucosa in ulcerative colitis (UC) is replete with antibody producing plasma B cells and polymorphonuclear leucocytes (PMN). This combination of effector cells requires a crosslinking antigen to evoke an antibody driven PMN inflammatory response via their Fc receptors. The stimulus for activation is thought to be commensal bacteria colonising the gut mucosa. The aim of this investigation was to compare the principal culturable bacterial populations on the rectal mucosa of UC patients, and to determine whether specific antibodies towards these bacteria can activate infiltrating PMN through opsonisation. This would provide an explanation for this chronic inflammatory condition.

methodsBacteria colonising rectal tissue were characterised using chemotaxonomic techniques. Systemic antibody responses were measured against total antigens and surface antigens of these organisms in UC and Crohn's disease (CD) patients, together with healthy controls. Antibody enhancement of the respiratory burst in PMN was also investigated, against a range of mucosal isolates.

resultsDistinct differences were observed in some bacterial populations in UC biopsies, which were generally reflected in antibody responses towards these organisms. UC patients had higher IgG responses to surface antigens, primarily IgG1, whereas the response in CD was mainly IgG2. Antibodies from UC patients greatly enhanced the respiratory burst in PMN, in response to individual bacterial species.

conclusionsChanges in mucosal bacteria, and a switch from internal to surface antigen/antibody reactivity of a predominantly IgG1 type, leads to greater opsonisation of the respiratory burst in PMN, providing a mechanism for maintaining the inflammatory state in UC.

Indexed as

AgedAged, 80 and overAntibodies, BacterialAntigens, BacterialAntigens, SurfaceBacteriaColitis, UlcerativeCrohn DiseaseFemaleHumansImmunity, MucosalImmunoglobulin AImmunoglobulin GIntestinal MucosaMaleMiddle AgedAntibodies, BacterialAntigens, BacterialAntigens, SurfaceImmunoglobulin AImmunoglobulin G

Identifiers

PMID14684582
PMCPMC1773925
OpenAlexW2145291631

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.