Evidence map›Paper›PMID 22267601›Full record

ArticleGut2013

Ectopic lymphoid tissue alters the chemokine gradient, increases lymphocyte retention and exacerbates murine ileitis.

Eóin N McNamee, Joanne C Masterson, Paul Jedlicka, Colm B Collins, Ifor R Williams, Jesús Rivera-Nieves

Abstract read
In one paragraph

Article in Gut, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

30 citing papers in PubMed, 56 citations in OpenAlex.

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  17. Sphingosine-1-phosphate receptor-1 (S1PMucosal immunology · 2017
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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 3 institutions in 1 country.

Eóin N McNameeMucosal Inflammation Program, School of Medicine, Aurora, Colorado, USA.
Joanne C Masterson
Paul Jedlicka
Colm B Collins
Ifor R Williams
Jesús Rivera-Nieves
University of Colorado Denver · USEmory University · USUniversity of California, San Diego · US

Funding

CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR025780 · NCRR · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2008 to 2011
$61.3M
Regulation of Organized Intestinal Lymphoid Tissues by TRANCE/RANKLR01DK064730 · NIDDK · EMORY UNIVERSITY · PI WILLIAMS, IFOR R · 2004 to 2012
$2.7M
Targeting L-Selectin in Chronic Murine IleitisR01DK080212 · NIDDK · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI RIVERA-NIEVES, JESUS · 2009 to 2013
$1.7M
NCRR NIH HHS UL1 RR025780NIDDK NIH HHS DK080212NIDDK NIH HHS R01 DK064730NIDDK NIH HHS R01 DK080212
6 · The paper itself

Abstract

backgroundThe earliest endoscopically-evident lesion in Crohn's disease is the aphthous ulcer, which develops over ectopic lymphoid tissues (ie, inducible lymphoid follicles (ILF), tertiary lymphoid tissue (TLT)) in the chronically inflamed intestine. ILF/TLT are induced within effector sites by homeostatic lymphoid chemokines, but their role in the development of intestinal ILF/TLT and in the pathogenesis of Crohn's disease is poorly understood.

designUsing a mouse model of Crohn's-like ileitis (TNFARE) which develops florid induction of ILF/TLT within its terminal ileum, the contribution of the CCR7/CCL19/CCL21 chemokine axis during the development of TLT and its role in disease pathogenesis were assessed.

resultsBoth CCL19 and CCL21 were increased within the inflamed ileum of TNFARE mice, which resulted in CCR7 internalisation and impaired T cell chemotaxis. ILF/TLT were a major source of CCL19 and CCL21 and increased local synthesis, augmented recruitment/retention of effector, naïve and central memory T cell subsets within the inflamed ileum. Immunoblockade of CCR7 resulted in further effector T cell retention and exacerbation of ileitis.

conclusionsInduction of ILF/TLT in the chronically inflamed intestine alters the homeostatic CCL19-CCL21 lymphoid-chemokine gradient and increases recruitment/retention of effector CCR7+ T cell subsets within the terminal ileum, contributing to the perpetuation of chronic inflammation. Thus, blockade of CCR7 or its ligands might result in deleterious consequences for subjects with chronic inflammatory diseases.

Indexed as

AnimalsBiomarkersChemokine CCL19Chemokine CCL21Chemotaxis, LeukocyteChoristomaCrohn DiseaseDisease Models, AnimalEnzyme-Linked Immunosorbent AssayFlow CytometryFluorescent Antibody TechniqueHumansIleitisLymphoid TissueMiceMice, Mutant StrainsBiomarkersCcl19 protein, mouseCcr7 protein, mouseChemokine CCL19Chemokine CCL21Receptors, CCR7

Identifiers

PMID22267601
PMCPMC3726216
OpenAlexW2159940376

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.