Evidence map›Paper›PMID 15730387›Full record

ArticleClinical and experimental immunology2005

Increased lymphocyte trafficking to colonic microvessels is dependent on MAdCAM-1 and C-C chemokine mLARC/CCL20 in DSS-induced mice colitis.

K Teramoto, S Miura, Y Tsuzuki, R Hokari, C Watanabe, T Inamura, T Ogawa, N Hosoe, H Nagata, H Ishii and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical and experimental immunology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

19 citing papers in PubMed, 60 citations in OpenAlex.

  1. Trial
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  5. Article
  6. β7 Integrin Inhibition Can Increase Intestinal Inflammation by Impairing Homing of CD25Cellular and molecular gastroenterology and hepatology · 2020
    Article
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  9. Article
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  13. Interleukin-21 triggers effector cell responses in the gut.World journal of gastroenterology · 2010
    Review
  14. Article
  15. Review
  16. Article
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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 2 institutions in 1 country.

K TeramotoDepartment of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.
S Miura
Y Tsuzuki
R Hokari
C Watanabe
T Inamura
T Ogawa
N Hosoe
H Nagata
H Ishii
T Hibi
Keio University · JPNational Defense Medical College · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although enhanced lymphocyte trafficking is associated with colitis formation, little information about its regulation is available. The aim of this study was to examine how the murine liver and activation-regulated chemokine (mLARC/CCL20) contributes to lymphocyte recruitment in concert with vascular adhesion molecules in murine chronic experimental colitis. T and B lymphocytes isolated from the spleen were fluorescence-labelled and administered to recipient mice. Lymphocyte adhesion to microvessels of the colonic mucosa and submucosa was observed with an intravital microscope. To induce colitis, the mice received two cycles of treatment with 2% dextran sodium sulphate (DSS). In some of the experiments antibodies against the adhesion molecules or anti-mLARC/CCL20 were administered, or CC chemokine receptor 6 (CCR6) of the lymphocytes was desensitized with excess amounts of mLARC/CCL20. Significant increases in T and B cell adhesion to the microvessels of the DSS-treated mucosa and submucosa were observed. In chronic colitis, the accumulation of lymphocytes was significantly inhibited by anti-mucosal addressin cell adhesion molecule (MAdCAM)-1 mAb, but not by anti-vascular cell adhesion molecule-1. In DSS-treated colonic tissue, the expression of mLARC/CCL20 was significantly increased, the blocking of mLARC/CCL20 by monoclonal antibody or the desensitization of CCR6 with mLARC/CCL20 significantly attenuated the DSS-induced T and B cell accumulation. However, the combination of blocking CCR6 with MAdCAM-1 did not further inhibit these accumulations. These results suggest that in chronic DSS-induced colitis, both MAdCAM-1 and mLARC/CCL20 may play important roles in T and B lymphocyte adhesion in the inflamed colon under flow conditions.

Indexed as

AnimalsAntibodies, MonoclonalB-LymphocytesCell AdhesionCell Adhesion MoleculesCell MovementChemokine CCL20Chemokines, CCChronic DiseaseColitisColonDextran SulfateImmunoglobulinsImmunohistochemistryIntestinal MucosaLymphocyte ActivationAntibodies, MonoclonalCCL20 protein, mouseCCR6 protein, mouseCell Adhesion MoleculesChemokine CCL20Chemokines, CCDextran SulfateImmunoglobulinsMacrophage Inflammatory ProteinsMadcam1 protein, mouseMucoproteinsReceptors, CCR6Receptors, Chemokine

Identifiers

PMID15730387
PMCPMC1809314
OpenAlexW2001473914

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.