Evidence map›Paper›PMID 25412496›Full record

ArticlePLoS neglected tropical diseases2014

Differential dermal expression of CCL17 and CCL18 in tuberculoid and lepromatous leprosy.

William R Berrington, Chhatra B Kunwar, Kapil Neupane, Susan J F van den Eeden, James C Vary, Glenna J Peterson, Richard D Wells, Annemieke Geluk, Deanna A Hagge, Thomas R Hawn

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-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

9 citing papers in PubMed, 11 citations in OpenAlex.

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  9. Coming of Age--CC Chemokine Ligand 18 in ANCA-Associated Vasculitis.Journal of the American Society of Nephrology : JASN · 2015
    Article
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

10 authors at 3 institutions in 3 countries.

William R BerringtonUniversity of Washington School of Medicine, Seattle, Washington, United States of America.
Chhatra B KunwarMycobacterial Research Laboratory, Anandaban Hospital, Kathmandu, Nepal.
Kapil NeupaneMycobacterial Research Laboratory, Anandaban Hospital, Kathmandu, Nepal.
Susan J F van den EedenDepartment of Infectious Diseases, Leiden University Medical Center, Leiden, The Netherlands.
James C VaryUniversity of Washington School of Medicine, Seattle, Washington, United States of America.
Glenna J PetersonUniversity of Washington School of Medicine, Seattle, Washington, United States of America.
Richard D WellsUniversity of Washington School of Medicine, Seattle, Washington, United States of America.
Annemieke GelukDepartment of Infectious Diseases, Leiden University Medical Center, Leiden, The Netherlands.
Deanna A HaggeMycobacterial Research Laboratory, Anandaban Hospital, Kathmandu, Nepal.
Thomas R HawnUniversity of Washington School of Medicine, Seattle, Washington, United States of America.
University of Washington · USAnandaban Hospital · NPLeiden University Medical Center · NL

Funding

Innate Immunogenetics & Human InfectionsK24AI089794 · NIAID · UNIVERSITY OF WASHINGTON · PI HAWN, THOMAS R · 2010 to 2014
$746k
The Role of Nod1 and Nod2 in the Pathogeneisis of Legionella Pneumophila PneumoniK08AI080952 · NIAID · UNIVERSITY OF WASHINGTON · PI BERRINGTON, WILLIAM RICHARD · 2009 to 2012
$623k
NIAID NIH HHS 1K24AI089794NIAID NIH HHS AI080952NIAID NIH HHS K08 AI080952NIAID NIH HHS K24 AI089794
6 · The paper itself

Abstract

backgroundLeprosy is characterized by polar clinical, histologic and immunological presentations. Previous immunologic studies of leprosy polarity were limited by the repertoire of cytokines known at the time. METHODOLOGY: We used a candidate gene approach to measure mRNA levels in skin biopsies from leprosy lesions. mRNA from 24 chemokines and cytokines, and 6 immune cell type markers were measured from 85 Nepalese leprosy subjects. Selected findings were confirmed with immunohistochemistry. PRINCIPAL

resultsExpression of three soluble mediators (CCL18, CCL17 and IL-10) and one macrophage cell type marker (CD14) was significantly elevated in lepromatous (CCL18, IL-10 and CD14) or tuberculoid (CCL17) lesions. Higher CCL18 protein expression by immunohistochemistry and a trend in increased serum CCL18 in lepromatous lesions was observed. No cytokines were associated with erythema nodosum leprosum or Type I reversal reaction following multiple comparison correction. Hierarchical clustering suggested that CCL18 was correlated with cell markers CD209 and CD14, while neither CCL17 nor CCL18 were highly correlated with classical TH1 and TH2 cytokines.

conclusionsOur findings suggest that CCL17 and CCL18 dermal expression is associated with leprosy polarity.

Indexed as

AdultBiomarkersChemokine CCL17Chemokines, CCCluster AnalysisErythema NodosumFemaleGene Expression Regulation, BacterialHumansInterleukin-10Leprosy, LepromatousLeprosy, TuberculoidMacrophagesMaleMiddle AgedSkinBiomarkersCCL17 protein, humanCCL18 protein, humanChemokine CCL17Chemokines, CCIL10 protein, humanInterleukin-10

Identifiers

PMID25412496
PMCPMC4238987
OpenAlexW2095460643

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.