Evidence map›Paper›PMID 26568315›Full record

ArticleeLife2015

Bystander hyperactivation of preimmune CD8+ T cells in chronic HCV patients.

Cécile Alanio, Francesco Nicoli, Philippe Sultanik, Tobias Flecken, Brieuc Perot, Darragh Duffy, Elisabetta Bianchi, Annick Lim, Emmanuel Clave, Marit M van Buuren and 14 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in eLife, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01534728 (Identification of HCV Specific T Cells Using Tetramer Technology - TETRA Study), which is not on this map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing 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.

NCT01534728 completednot on this map

Identification of HCV Specific T Cells Using Tetramer Technology - TETRA Study

TypeobservationalSponsorInstitut National de la Santé Et de la Recherche Médicale, FranceRan2012 to 2014Enrolled40ConditionsHepatitis C
3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 56 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Bystander activated CD8Nature communications · 2024
    Article
  6. IL-15-induced CD38Clinical & translational immunology · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Altered Basal Lipid Metabolism Underlies the Functional Impairment of Naive CD8Journal of immunology (Baltimore, Md. : 1950) · 2022
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. CXCR3 Identifies Human Naive CD8Journal of immunology (Baltimore, Md. : 1950) · 2019
    Article
  20. The activation of bystander CD8Experimental & molecular medicine · 2019
    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

24 authors at 13 institutions in 4 countries.

Cécile AlanioUnités de Recherche Internationales Mixtes Pasteur, Institut Pasteur, Paris, France.
Francesco NicoliSorbonne Universités, UPMC Univ Paris 06, DNU FAST, CR7, Centre d'Immunologie et des Maladies Infectieuses (CIMI-Paris), Paris, France.
Philippe SultanikUnités de Recherche Internationales Mixtes Pasteur, Institut Pasteur, Paris, France.
Tobias FleckenThe University Medical Center Freiburg, Department of Internal Medicine II, Albert-Ludwigs-Universität, Freiberg, Germany.
Brieuc PerotUnités de Recherche Internationales Mixtes Pasteur, Institut Pasteur, Paris, France.
Darragh DuffyUnités de Recherche Internationales Mixtes Pasteur, Institut Pasteur, Paris, France.
Elisabetta BianchiImmunoregulation Unit, Institut Pasteur, Paris, France.
Annick LimPlateforme d'Immunoscope, Institut Pasteur, Paris, France.
Emmanuel ClaveHôpital Saint-Louis, Assistance publique - hôpitaux de Paris, Paris, France.
Marit M van BuurenDepartment of Immunology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Aurélie SchnurigerLaboratoire de virologie, Hôpital Armand-Trousseau, Assistance publique - hôpitaux de Paris, Paris, France.
Kerstin JohnssonMathematics, Faculty of Engineering, Lunds University, Lund, Sweden.
Jeremy BoussierUnités de Recherche Internationales Mixtes Pasteur, Institut Pasteur, Paris, France.
Antoine Garbarg-ChenonLaboratoire de virologie, Hôpital Armand-Trousseau, Assistance publique - hôpitaux de Paris, Paris, France.
Laurence BousquetAPHP, Université Paris Descartes, Paris, France.
Estelle MottezCentre d'Immunologie Humaine, Institut Pasteur, Paris, France.
Ton N SchumacherDepartment of Immunology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Antoine ToubertHôpital Saint-Louis, Assistance publique - hôpitaux de Paris, Paris, France.
Victor AppaySorbonne Universités, UPMC Univ Paris 06, DNU FAST, CR7, Centre d'Immunologie et des Maladies Infectieuses (CIMI-Paris), Paris, France.
Farhad HeshmatiEFS, Hôpital Cochin, Paris, France.
Robert ThimmeThe University Medical Center Freiburg, Department of Internal Medicine II, Albert-Ludwigs-Universität, Freiberg, Germany.
Stanislas PolAPHP, Université Paris Descartes, Paris, France.
Vincent MalletAPHP, Université Paris Descartes, Paris, France.
Matthew L AlbertUnités de Recherche Internationales Mixtes Pasteur, Institut Pasteur, Paris, France.
Institut Pasteur · FRCentre d'Immunologie et des Maladies Infectieuses · FRHôpital Saint-Louis · FRUniversity of Freiburg · DEAssistance Publique – Hôpitaux de Paris · FRDélégation Paris 5 · FRHôpital Armand-Trousseau · FRHôpital Cochin · FRLund University · SEOncode Institute · NLSorbonne Université · FRThe Netherlands Cancer Institute · NLUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic infection perturbs immune homeostasis. While prior studies have reported dysregulation of effector and memory cells, little is known about the effects on naïve T cell populations. We performed a cross-sectional study of chronic hepatitis C (cHCV) patients using tetramer-associated magnetic enrichment to study antigen-specific inexperienced CD8(+) T cells (i.e., tumor or unrelated virus-specific populations in tumor-free and sero-negative individuals). cHCV showed normal precursor frequencies, but increased proportions of memory-phenotype inexperienced cells, as compared to healthy donors or cured HCV patients. These observations could be explained by low surface expression of CD5, a negative regulator of TCR signaling. Accordingly, we demonstrated TCR hyperactivation and generation of potent CD8(+) T cell responses from the altered T cell repertoire of cHCV patients. In sum, we provide the first evidence that naïve CD8(+) T cells are dysregulated during cHCV infection, and establish a new mechanism of immune perturbation secondary to chronic infection.

Indexed as

Lymphocyte ActivationCD5 AntigensCD8-Positive T-LymphocytesCross-Sectional StudiesHepacivirusHepatitis C, ChronicHumansReceptors, Antigen, T-CellSignal TransductionCD5 AntigensReceptors, Antigen, T-CellCD8 T cell dysfunctionchronic inflammationhumanhuman biologyimmunologymedicinePre-immune repertoireTCR signalingviral immunology

Identifiers

PMID26568315
PMCPMC4752008
OpenAlexW2245303435

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.