Evidence map›Paper›PMID 23873879›Full record

ArticleAnnals of the rheumatic diseases2014

Global chemokine expression in systemic sclerosis (SSc): CCL19 expression correlates with vascular inflammation in SSc skin.

Allison L Mathes, Romy B Christmann, Giuseppina Stifano, Alsya J Affandi, Timothy R D J Radstake, G Alessandra Farina, Cristina Padilla, Sarah McLaughlin, Robert Lafyatis

Open access · greenAbstract read
In one paragraph

Article in Annals of the rheumatic diseases, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

35 citing papers in PubMed, 67 citations in OpenAlex.

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  7. Methylation of T and B Lymphocytes in Autoimmune Rheumatic Diseases.Clinical reviews in allergy & immunology · 2024
    Review
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  15. Review
  16. Review
  17. Review
  18. Article
  19. Review
  20. The immunopathogenesis of fibrosis in systemic sclerosis.Clinical and experimental immunology · 2019
    Review
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

9 authors at 2 institutions in 2 countries.

Allison L MathesRheumatology Section, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts, USA.
Romy B ChristmannRheumatology Section, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts, USA.
Giuseppina StifanoRheumatology Section, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts, USA.
Alsya J AffandiRheumatology Section, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts, USA Department of Rheumatology and Clinical Immunology, University Medical Center Utrecht, Utrecht, The Netherlands.
Timothy R D J RadstakeRheumatology Section, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts, USA Department of Rheumatology and Clinical Immunology, University Medical Center Utrecht, Utrecht, The Netherlands.
G Alessandra FarinaRheumatology Section, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts, USA.
Cristina PadillaRheumatology Section, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts, USA.
Sarah McLaughlinRheumatology Section, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts, USA.
Robert LafyatisRheumatology Section, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts, USA.
Boston University · USUniversity Medical Center Utrecht · NL

Funding

WORK DISABILITY-- PERSONS WITH RHEUMATOID ARTHRITISP60AR047785 · NIAMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI FELSON, DAVID TOBIN · 2001 to 2016
$18.0M
Translational studies for identifying and targeting novel pathways in systemic sclerosis pathogenesisP50AR060780 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DOMSIC, ROBYN THERESE · 2011 to 2021
$14.9M
RESEARCH TRAINING IN IMMUNOLOGYT32AI007309 · NIAID · BOSTON UNIVERSITY MEDICAL CAMPUS · PI GUMMULURU, SURYARAM · 1988 to 2024
$7.4M
Rheumatic Diseases Research Core CentersP30AR061271 · NIAMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI WHITFIELD, MICHAEL L · 2011 to 2015
$3.1M
Innate immunity in dermal fibrosis and systemic sclerosisR01AR051089 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LAFYATIS, ROBERT A. · 2005 to 2015
$2.8M
RHEUMATOLOGY TRAINING GRANTT32AR007598 · NIAMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI FELSON, DAVID TOBIN · 1997 to 2018
$2.3M
Interplay between Type I IFN and TGF-beta signaling in systemic sclerosisR03AR062721 · NIAMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI FARINA, GIUSEPPINA ALESSANDRA · 2012 to 2014
$240k
NIAID NIH HHS 5T32 AI007309NIAID NIH HHS T32 AI007309NIAMS NIH HHS 1P50AR060780NIAMS NIH HHS 2R01AR051089NIAMS NIH HHS P30 AR061271NIAMS NIH HHS P50 AR060780NIAMS NIH HHS P60 AR047785NIAMS NIH HHS R01 AR051089NIAMS NIH HHS R03 AR062721NIAMS NIH HHS T32 AR007598
6 · The paper itself

Abstract

objectiveTo characterise global chemokine expression in systemic sclerosis (SSc) skin in order to better understand the relationship between chemokine expression and vascular inflammation in this disease.

methodsWe investigated chemokine mRNA expression in the skin through quantitative PCR analysis comparing patients with diffuse cutaneous (dcSSc) or limited cutaneous (lcSSc) disease with healthy controls. We tested correlations between the most regulated chemokines and vascular inflammation and macrophage recruitment. CCL19 expression was examined in human primary immune cells treated with innate immune activators.

resultsThe chemokines, CCL18, CCL19 and CXCL13, were upregulated in dcSSc skin, and CCL18 in lcSSc skin. Expression of CCL19 in dcSSc skin correlated with markers of vascular inflammation and macrophage recruitment. Immunofluorescence data showed CCL19 colocalisation with CD163 macrophages in dcSSc skin. In vitro studies on human primary cells demonstrated that CCL19 expression was induced after toll-like receptor activation of peripheral blood mononuclear cells and separated populations of CD14 monocytes.

conclusionsCCL18, CCL19 and CXCL13-chemoattractants for macrophage and T cell recruitment-were three of six chemokines with the highest expression in dcSSc skin. Increased CCL19 expression in the skin suggests a role for CCL19 in the recruitment of immune cells to the peripheral tissue. Induction of CCL19 in macrophages but not structural cells indicates a role for skin-resident or recruited immune cells in perivascular inflammation. This study demonstrates that CCL19 is a sensitive marker for the perivascular inflammation and immune cell recruitment seen in dcSSc skin disease.

Indexed as

AdultAgedBiomarkersCase-Control StudiesCells, CulturedChemokine CCL19ChemokinesFemaleGene ExpressionGene Expression ProfilingHumansImmunity, InnateLeukocytes, MononuclearMacrophage ActivationMaleMiddle AgedBiomarkersCCL19 protein, humanChemokine CCL19ChemokinesRNA, MessengerChemokinesInflammationSystemic Sclerosis

Identifiers

PMID23873879
PMCPMC4076390
OpenAlexW2115443085

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.