Evidence map›Paper›PMID 19193669›Full record

ArticleGut2009

Impaired plasmacytoid dendritic cell maturation and differential chemotaxis in chronic hepatitis C virus: associations with antiviral treatment outcomes.

J A Mengshol, L Golden-Mason, N Castelblanco, K A Im, S M Dillon, C C Wilson, H R Rosen, Virahep-C Study Group

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in Gut, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

25 citing papers in PubMed, 45 citations in OpenAlex.

  1. Trial
  2. Article
  3. Mononuclear phagocyte system in hepatitis C virus infection.World journal of gastroenterology · 2018
    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

8 authors at 3 institutions in 1 country.

J A MengsholDivision of Gastroenterology and Hepatology, Department of Medicine, University of Colorado Denver, Colorado, USA.
L Golden-Mason
N Castelblanco
K A Im
S M Dillon
C C Wilson
H R Rosen
Virahep-C Study Group
University of Colorado Denver · USHepatitis B Foundation · USUniversity of Pittsburgh · US

Funding

Study of Viral Resistance to Antiviral Therapy of Chron*U01DK060329 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BELLE, STEVEN H. · 2001 to 2005
$8.0M
GASTROINTESTINAL DISEASE TRAINING GRANTT32DK007038 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI COLGAN, SEAN P · 1986 to 2020
$3.5M
Response of HCV to Therapy in African AmericansU01DK060345 · NIDDK · SAINT LOUIS UNIVERSITY · PI TAVIS, JOHN E · 2001 to 2005
$1.4M
HCV TREATMENT IN AFRICAN AMERICANS VS NON HISPANIC WHIT*U01DK060352 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI JEFFERS, LENNOX J · 2001 to 2005
$1.4M
Innate Immune Responses During Therapy for Chronic HCVR01DK071560 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI ROSEN, HUGO RAMON · 2005 to 2009
$1.4M
Hepatitis C: host determinants of progression and respo*U01DK060341 · NIDDK · CEDARS-SINAI MEDICAL CENTER · PI YANG, HUIYING · 2001 to 2005
$1.4M
VIRAHEP-C Clinical CenterU01DK060344 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LOK, ANNA SF · 2001 to 2005
$1.3M
Baltimore VIRAHEP-C Clinical CenterU01DK060335 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI HOWELL, CHARLES D · 2001 to 2005
$1.3M
Hepatitis C Antiviral Resistance in African AmericansU01DK060327 · NIDDK · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI FRIED, MICHAEL W · 2001 to 2005
$1.2M
Antiviral Therapy in African Americans with HCVU01DK060340 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI AFDHAL, NEZAM HASSAN · 2001 to 2005
$1.2M
Differential cytokine responses in Hep C patients.U01DK060309 · NIDDK · INDIANA UNIVERSITY BLOOMINGTON · PI TAYLOR, MILTON W · 2001 to 2005
$1.2M
Race &Viral Resistance in Chronic Hepatitis C (VIRAHEP*U01DK060324 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI BROWN, ROBERT S · 2001 to 2005
$1.2M
Intramural NIH HHSNIDDK NIH HHS R01 DK071560NIDDK NIH HHS T32 DK007038NIDDK NIH HHS T32 DK7038-32NIDDK NIH HHS U01 DK060309NIDDK NIH HHS U01 DK060324NIDDK NIH HHS U01 DK060327NIDDK NIH HHS U01 DK060329NIDDK NIH HHS U01 DK060335NIDDK NIH HHS U01 DK060340NIDDK NIH HHS U01 DK060341NIDDK NIH HHS U01 DK060342NIDDK NIH HHS U01 DK060344NIDDK NIH HHS U01 DK060345NIDDK NIH HHS U01 DK060346NIDDK NIH HHS U01 DK060349NIDDK NIH HHS U01 DK060352NIDDK NIH HHS U01 DK60309NIDDK NIH HHS U01 DK60324NIDDK NIH HHS U01 DK60327NIDDK NIH HHS U01 DK60329NIDDK NIH HHS U01 DK60335NIDDK NIH HHS U01 DK60340NIDDK NIH HHS U01 DK60341NIDDK NIH HHS U01 DK60342NIDDK NIH HHS U01 DK60344NIDDK NIH HHS U01 DK60345NIDDK NIH HHS U01 DK60346NIDDK NIH HHS U01 DK60349NIDDK NIH HHS U01 DK60352
6 · The paper itself

Abstract

backgroundDendritic cell (DC) defects may contribute to chronicity in hepatitis C virus (HCV) infection and determine response to PEG-interferon and ribavirin therapy via poor T cell stimulation. Studies to date have produced inconsistent results regarding DC maturation and function: no large study has examined DCs before and after therapy.

aimsWe examined if DC defects in maturation and chemotaxis are present by comparing therapeutic responders to non-responders.

methodsWe analysed peripheral DCs of 64 HCV genotype 1-infected patients from the Virahep-C study 2 weeks before and 24 weeks after therapy. We used flow cytometry to enumerate plasmacytoid DC (pDC) and myeloid DCs (mDC) and quantify expression of chemokine receptors and maturation markers. Chemotaxis was measured with an in vitro assay.

resultsPre-treatment frequencies of pDCs and mDCs were significantly lower in HCV patients than controls and successful therapy normalised pDCs. Levels of CXCR3 and CXCR4 on pDCs were higher at baseline compared to normal controls and decreased with therapy. Pre-therapy levels of co-stimulatory marker CD40 and the maturation marker CD83 were higher in pDCs of patients chronically infected with HCV compared to normal patients, and levels of both markers dropped significantly with therapy in the SVR+ group only. Other maturation markers (CD86 and CCR7) were not elevated suggesting a partially activated phenotype. Baseline chemotaxis of pDCs to CXCL12 and CXCL10 predicted failure of antiviral response and correlated with the histological activity index inflammation score.

conclusionsPlasmacytoid DC defects exist in chronic HCV and successful antiviral therapy normalises many phenotypic and functional abnormalities.

Indexed as

AdultAntiviral AgentsChemotaxisDendritic CellsFemaleFlow CytometryGenotypeHepatitis C, ChronicHumansMaleMiddle AgedReceptors, ChemokineT-LymphocytesTreatment OutcomeAntiviral AgentsReceptors, Chemokine

Identifiers

PMID19193669
PMCPMC2689392
OpenAlexW2135556328

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.