Evidence map›Paper›PMID 20548953›Full record

ArticlePLoS pathogens2010

Coexpression of PD-1, 2B4, CD160 and KLRG1 on exhausted HCV-specific CD8+ T cells is linked to antigen recognition and T cell differentiation.

Bertram Bengsch, Bianca Seigel, Marianne Ruhl, Jörg Timm, Martin Kuntz, Hubert E Blum, Hanspeter Pircher, Robert Thimme

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 233 papers.

0numbers the graph read from it
0cells of the map it votes in
233citing papers in PubMed
11.5field-weighted citation impact, top 1% 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

233 citing papers in PubMed, 367 citations in OpenAlex.

  1. Epigenetic scars of CD8Nature immunology · 2021
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  9. Review
  10. T cell adaptation in chronic infections and tumors.Cellular & molecular immunology · 2026
    Review
  11. Review
  12. Article
  13. Article
  14. Tissue-specific T cell profiles inFrontiers in tuberculosis · 2025
    Article
  15. Article
  16. The role of KLRG1: a novel biomarker and new therapeutic target.Cell communication and signaling : CCS · 2024
    Review
  17. Review
  18. PD-1Oncology research · 2024
    Article
  19. Article
  20. Article

173 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

Bertram BengschDepartment of Medicine II, University of Freiburg, Freiburg, Germany.
Bianca Seigel
Marianne Ruhl
Jörg Timm
Martin Kuntz
Hubert E Blum
Hanspeter Pircher
Robert Thimme
University of Freiburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Exhausted CD8+ T cell responses during chronic viral infections are defined by a complex expression pattern of inhibitory receptors. However, very little information is currently available about the coexpression patterns of these receptors on human virus-specific CD8+ T cells and their correlation with antiviral functions, T cell differentiation and antigen recognition. We addressed these important aspects in a cohort of 38 chronically HCV infected patients and found a coexpression of inhibitory receptors such as 2B4, CD160 and KLRG1 in association with PD-1 in about half of the HCV-specific CD8+ T cell responses. Importantly, this exhaustive phenotype was associated with low and intermediate levels of CD127 expression, an impaired proliferative capacity, an intermediate T cell differentiation stage and absence of sequence variations within the corresponding epitopes, indicating ongoing antigen triggering. In contrast, a low expression of inhibitory receptors by the remaining HCV-specific CD8+ T cells occurred in concert with a CD127hi phenotype, an early T cell differentiation stage and presence of viral sequence variations within the corresponding epitopes. In sum, these results suggest that T cell exhaustion contributes to the failure of about half of HCV-specific CD8+ T cell responses and that it is determined by a complex interplay of immunological (e.g. T cell differentiation) and virological (e.g. ongoing antigen triggering) factors.

Indexed as

Cell DifferentiationAntigens, CDApoptosis Regulatory ProteinsCD8-Positive T-LymphocytesCell ProliferationFlow CytometryGPI-Linked ProteinsHepacivirusHepatitis CHumansLectins, C-TypeLymphocyte ActivationProgrammed Cell Death 1 ReceptorReceptors, ImmunologicSignaling Lymphocytic Activation Molecule FamilyT-LymphocytesAntigens, CDApoptosis Regulatory ProteinsCD160 protein, humanCD244 protein, humanGPI-Linked ProteinsKLRG1 protein, humanLectins, C-TypePDCD1 protein, humanProgrammed Cell Death 1 ReceptorReceptors, ImmunologicSignaling Lymphocytic Activation Molecule FamilyTrans-Activators

Identifiers

PMID20548953
PMCPMC2883597
OpenAlexW1975753196

What OpenQuestion holds

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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.