Evidence map›Paper›PMID 17239662›Full record

ArticleClinical immunology (Orlando, Fla.)2007

Differential dysfunction in dendritic cell subsets during chronic HCV infection.

Lynn Averill, William M Lee, Nitin J Karandikar

Abstract read
In one paragraph

Article in Clinical immunology (Orlando, Fla.), 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

43 citing papers in PubMed, 79 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Mononuclear phagocyte system in hepatitis C virus infection.World journal of gastroenterology · 2018
    Review
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  6. Article
  7. Article
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  9. Article
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  11. Review
  12. Review
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  14. O death where is thy sting? Immunologic tolerance to apoptotic self.Cellular and molecular life sciences : CMLS · 2013
    Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. 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

3 authors at 1 institution in 1 country.

Lynn AverillDepartment of Pathology, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
William M Lee
Nitin J Karandikar
The University of Texas Southwestern Medical Center · US

Funding

MEMORY AND EFFECTOR CTL RESPONSES TO VIRUS INFECTIONSR01AI047603 · NIAID · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI KARANDIKAR, NITIN J · 1999 to 2002
$667k
NIAID NIH HHS R01 AI047603NIAID NIH HHS R01AI047603
6 · The paper itself

Abstract

Hepatitis C virus (HCV) infection is a leading cause of chronic liver disease with over 200 million individuals infected worldwide. The vast majority of acutely infected humans develop chronic infection, which is characterized by attenuated antiviral T-cell responses. The mechanisms leading to such attenuation/suppression are poorly understood. It has been proposed that dysfunction of antigen-presenting cells (APC) may underlie the downregulation of antiviral immune responses. However, studies using bulk or in vitro-derived APC populations have resulted in conflicting reports. In this study, we evaluated the functional and immunophenotypic features of ex vivo-purified dendritic cell (DC) subsets during chronic HCV infection. We found that plasmacytoid DC (PDC) from HCV-infected patients (HCV-PDC) showed a striking deficit in IFN-alpha production in response to CpG stimulation. In addition, we found that myeloid DC (MDC) from these patients showed a diminished capacity to induce a mixed lymphocyte response (MLR), correlating with lower levels of HLA-DR and CD86 expression and higher IL-10 production in response to poly-IC stimulation. In contrast, HCV-PDC showed increased ability to stimulate an MLR. Of note, within the HCV-PDC preparation, we noted a distinctly expanded DC subset that expressed some markers of MDC, but showed significantly lower HLA-DR and CD86 expression, suggesting an expansion of DC at an immature/intermediate stage of differentiation. Our studies demonstrate distinct and contrasting dysfunctional features in DC subsets and underscore the importance of evaluating APC subpopulations separately.

Indexed as

AdultAntigen PresentationB7-2 AntigenDendritic CellsEnzyme-Linked Immunosorbent AssayFemaleFlow CytometryHepatitis C, ChronicHLA-DR AntigensHumansInterferon-alphaInterleukin-10Interleukin-12Lymphocyte Culture Test, MixedMaleMiddle AgedB7-2 AntigenHLA-DR AntigensInterferon-alphaInterleukin-10Interleukin-12

Identifiers

PMID17239662
PMCPMC1865520
OpenAlexW2098964597

What OpenQuestion holds

Textmetadata
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.