Evidence map›Paper›PMID 17653276›Full record

ArticlePloS one2007

Tracking virus-specific CD4+ T cells during and after acute hepatitis C virus infection.

Michaela Lucas, Axel Ulsenheimer, Katja Pfafferot, Malte H J Heeg, Silvana Gaudieri, Norbert Grüner, Andri Rauch, J Tilman Gerlach, Maria-Christina Jung, Reinhart Zachoval and 16 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.6field-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

34 citing papers in PubMed, 70 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Trial
  5. Article
  6. Article
  7. Characterizing Hepatitis C Virus-Specific CD4Hepatology (Baltimore, Md.) · 2020
    Observational
  8. Adaptive Immune Response against Hepatitis C Virus.International journal of molecular sciences · 2020
    Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Evidence of CD4Scientific reports · 2018
    Article
  15. CD4Trends in molecular medicine · 2017
    Review
  16. Adaptive immunity in the liver.Cellular & molecular immunology · 2016
    Review
  17. Review
  18. Review
  19. Article
  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

26 authors at 10 institutions in 6 countries.

Michaela LucasPeter Medawar Building for Pathogen Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom; Centre for Clinical Immunology and Biomedical Statistics, Royal Perth Hospital and Murdoch University, Perth, Australia.
Axel Ulsenheimer
Katja Pfafferot
Malte H J Heeg
Silvana Gaudieri
Norbert Grüner
Andri Rauch
J Tilman Gerlach
Maria-Christina Jung
Reinhart Zachoval
Gerd R Pape
Winfried Schraut
Teresa Santantonio
Hans Nitschko
Martin Obermeier
Rodney Phillips
Thomas J Scriba
Nasser Semmo
Cheryl Day
Jonathan N Weber
Sarah Fidler
Robert Thimme
Anita Haberstroh
Thomas F Baumert
Paul Klenerman
Helmut M Diepolder
Ludwig-Maximilians-Universität München · DEMedawar Building for Pathogen Research · GBSt Mary's Hospital · GBUniversity of Freiburg · DEUniversity of Oxford · GBInserm · FRMurdoch University · AURoyal Perth Hospital · AUUniversity Hospital of Bern · CHUniversity of Bari Aldo Moro · IT

Funding

Wellcome Trust
6 · The paper itself

Abstract

backgroundCD4+ T cell help is critical in maintaining antiviral immune responses and such help has been shown to be sustained in acute resolving hepatitis C. In contrast, in evolving chronic hepatitis C CD4+ T cell helper responses appear to be absent or short-lived, using functional assays. METHODOLOGY/PRINCIPAL

findingsHere we used a novel HLA-DR1 tetramer containing a highly targeted CD4+ T cell epitope from the hepatitis C virus non-structural protein 4 to track number and phenotype of hepatitis C virus specific CD4+ T cells in a cohort of seven HLA-DR1 positive patients with acute hepatitis C in comparison to patients with chronic or resolved hepatitis C. We observed peptide-specific T cells in all seven patients with acute hepatitis C regardless of outcome at frequencies up to 0.65% of CD4+ T cells. Among patients who transiently controlled virus replication we observed loss of function, and/or physical deletion of tetramer+ CD4+ T cells before viral recrudescence. In some patients with chronic hepatitis C very low numbers of tetramer+ cells were detectable in peripheral blood, compared to robust responses detected in spontaneous resolvers. Importantly we did not observe escape mutations in this key CD4+ T cell epitope in patients with evolving chronic hepatitis C. CONCLUSIONS/SIGNIFICANCE: During acute hepatitis C a CD4+ T cell response against this epitope is readily induced in most, if not all, HLA-DR1+ patients. This antiviral T cell population becomes functionally impaired or is deleted early in the course of disease in those where viremia persists.

Indexed as

Acute DiseaseAmino Acid SequenceBase SequenceCD4-Positive T-LymphocytesDNA PrimersEpitopes, T-LymphocyteFemaleGenotypeHepacivirusHepatitis CHLA-DR1 AntigenHumansImmunity, CellularLiverMalePeptide FragmentsDNA PrimersEpitopes, T-LymphocyteHLA-DR1 AntigenPeptide FragmentsViral Proteins

Identifiers

PMID17653276
PMCPMC1920556
OpenAlexW2034116082

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.