Evidence map›Paper›PMID 22711645›Full record

ArticleHepatology (Baltimore, Md.)2012

Hepatic enrichment and activation of myeloid dendritic cells during chronic hepatitis C virus infection.

Victoria M Velazquez, Huiming Hon, Chris Ibegbu, Stuart J Knechtle, Allan D Kirk, Arash Grakoui

Open access · bronzeAbstract read
In one paragraph

Article in Hepatology (Baltimore, Md.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

23 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Myeloid Cells and Chronic Liver Disease: a Comprehensive Review.Clinical reviews in allergy & immunology · 2018
    Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Presentation of hepatocellular antigens.Cellular & molecular immunology · 2016
    Review
  13. Natural killer cells in hepatitis C: Current progress.World journal of gastroenterology · 2016
    Review
  14. Immunopathogenesis of Hepatitis C Virus Infection.Gastroenterology clinics of North America · 2015
    Review
  15. Human dendritic cell subsets and function in health and disease.Cellular and molecular life sciences : CMLS · 2015
    Review
  16. Review
  17. Article
  18. Human pDCs preferentially sense enveloped hepatitis A virions.The Journal of clinical investigation · 2015
    Article
  19. Review
  20. Immune tolerance in liver disease.Hepatology (Baltimore, Md.) · 2014
    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

6 authors at 1 institution in 1 country.

Victoria M VelazquezEmory Vaccine Center, Emory University School of Medicine, Atlanta, GA 30329, USA.
Huiming Hon
Chris Ibegbu
Stuart J Knechtle
Allan D Kirk
Arash Grakoui
Emory University · US

Funding

YNPRC NHP CLINICAL MEDICINE RESIDENCY PROGRAM - SUPPLEMENTP51RR000165 · NCRR · EMORY UNIVERSITY · PI ALTMAN, JOHN DAVID · 1985 to 2011
$114.0M
Virology and Molecular Biomarkers CoreP30AI050409 · NIAID · EMORY UNIVERSITY · PI Carlos del Rio · 2002 to 2026
$74.0M
TRAINING IN IMMUNOLOGY AND MOLECULAR PATHOGENESIST32AI007610 · NIAID · EMORY UNIVERSITY · PI EVAVOLD, BRIAN D · 2000 to 2014
$4.4M
Mechanisms of hepatitis C virus persistenceR01AI070101 · NIAID · EMORY UNIVERSITY · PI GRAKOUI, ARASH · 2006 to 2016
$3.9M
MOLECULAR MECHANISMS OF MICROBIAL PATHOGENESIST32AI007470 · NIAID · EMORY UNIVERSITY · PI SPECK, SAMUEL H · 1995 to 2010
$3.2M
Defining the intrahepatic immune response to hepatitis C virusR01DK083356 · NIDDK · EMORY UNIVERSITY · PI GRAKOUI, ARASH · 2010 to 2013
$1.5M
Mechanisms of hepatitis C virus persistenceR56AI070101 · NIAID · EMORY UNIVERSITY · PI GRAKOUI, ARASH · 2011 to 2011
$437k
NCRR NIH HHS P51 RR000165NCRR NIH HHS RR-00165NIAID NIH HHS AI070101NIAID NIH HHS P30 AI050409NIAID NIH HHS R01 AI070101NIAID NIH HHS R56 AI070101NIAID NIH HHS T32 AI007470NIAID NIH HHS T32 AI007610NIDDK NIH HHS DK083356NIDDK NIH HHS R01 DK083356
6 · The paper itself

Abstract

unlabelledChronic hepatitis C virus (HCV) infection is a serious disease that can result in numerous long-term complications leading to liver failure or death. Approximately 80% of people fail to clear their infection, largely as the result of weak, narrowly targeting or waning antiviral T-cell responses. Although professional antigen presenting cells (APCs) like dendritic cells (DCs) might serve as targets for modulation of T-cell immunity, the particular role of DCs in immunity to HCV is not known. Moreover the identity, phenotype, and functional characteristics of such populations in the liver, the site of HCV replication, have proven difficult to elucidate. Using a multicolor flow-based approach, we identified six distinct populations of professional APCs among liver interstitial leukocytes isolated from uninfected and HCV-infected patients. Although a generalized enrichment of DCs in the liver compared to blood was observed for all patients, HCV infection was characterized by a significant increase in the frequency of intrahepatic myeloid DCs (both CD1c+ and CD141+). Phenotypic analyses of liver plasmacytoid (pDC) and myeloid DCs (mDC) further revealed the HCV-induced expression of maturation molecules CD80, CD83, CD40, and programmed death ligand-1. Importantly, pDC and mDCs from HCV-infected liver were capable of secreting effector cytokines, interferon-alpha and interleukin-12, respectively, in response to Toll-like receptor stimulation in vitro.

conclusionChronic HCV infection facilitates the "customized" recruitment of liver DC subsets with established functional roles in antigen presentation. These DCs are characterized by a mature, activated phenotype and are functionally responsive to antigenic stimulation in vitro. Such findings highlight an important paradox surrounding liver DC recruitment during HCV infection, where despite their activation these cells do not provide adequate protection from the virus.

Indexed as

PhenotypeAntigens, CDAntigens, CD1B7-1 AntigenCD40 AntigensCD83 AntigenCell CountDendritic CellsFlow CytometryGlycoproteinsHepatitis C, ChronicHumansImmunoglobulinsInterferon-alphaInterleukin-12Leukocytes, Mononuclear1-(2-methylpropyl)-1H-imidazo(4,5-c)quinolin 4-amineAntigens, CDAntigens, CD1B7-1 AntigenCD1C protein, humanCD40 AntigensCD83 AntigenGlycoproteinsImmunoglobulinsInterferon-alphaInterleukin-12LipopolysaccharidesMembrane GlycoproteinsPDCD1 protein, humanProgrammed Cell Death 1 ReceptorQuinolinesThrombomodulin

Identifiers

PMID22711645
PMCPMC3747821
OpenAlexW2086087148

What OpenQuestion holds

Textmetadata
LicenceTDM
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.