Evidence map›Paper›PMID 18667516›Full record

ArticleJournal of virology2008

Early interferon therapy for hepatitis C virus infection rescues polyfunctional, long-lived CD8+ memory T cells.

Gamal Badr, Nathalie Bédard, Mohamed S Abdel-Hakeem, Lydie Trautmann, Bernard Willems, Jean-Pierre Villeneuve, Elias K Haddad, Rafick P Sékaly, Julie Bruneau, Naglaa H Shoukry

Registry-linked trialAbstract read
In one paragraph

Article in Journal of virology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01289496 (Ribavirin Dose Optimization for the Treatment of Hepatitis C), which is not on this map. Cited by 83 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 5% 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.

NCT01289496 phase2completednot on this mapstarted 2011, after this paper: background citation

Ribavirin Dose Optimization for the Treatment of Hepatitis C: A Pilot Study

TypeinterventionalSponsorCentre hospitalier de l'Université de Montréal (CHUM)Ran2011 to 2013Enrolled13ConditionsChronic Hepatitis CArmsPeg-interferon alpha-2a, Ribavirin
3 · Its place in the literature

Who cites it

83 citing papers in PubMed, 1 synthesis or guideline pooled it, 129 citations in OpenAlex.

  1. Transcriptional insights into the CD8Journal of translational medicine · 2020
    Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Functional Antigen-Specific CD8 TEuropean journal of immunology · 2025
    Article
  6. Review
  7. Immunomodulatory Role of Interferons in Viral and Bacterial Infections.International journal of molecular sciences · 2023
    Review
  8. Article
  9. Review
  10. Review
  11. Review
  12. Expansion of Unique Hepatitis C Virus-Specific Public CD8Journal of immunology (Baltimore, Md. : 1950) · 2021
    Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. Article

23 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

10 authors at 4 institutions in 2 countries.

Gamal BadrCentre de Recherche du Centre Hospitalier de l'Université de Montréal, Hôpital St.-Luc, 264 Blvd. René-Lévesque Est, Local PEA-316, Montréal (Québec) H2X 1P1, Canada.
Nathalie Bédard
Mohamed S Abdel-Hakeem
Lydie Trautmann
Bernard Willems
Jean-Pierre Villeneuve
Elias K Haddad
Rafick P Sékaly
Julie Bruneau
Naglaa H Shoukry
Hôpital Saint-Luc · CAUniversité de Montréal · CACentre Hospitalier de l’Université de Montréal · CAAssiut University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The majority of acute hepatitis C virus (HCV) infections progress to chronicity and progressive liver damage. Alpha interferon (IFN-alpha) antiviral therapy achieves the highest rate of success when IFN-alpha is administered early during the acute phase, but the underlying mechanisms are unknown. We used a panel of major histocompatibility complex class I tetramers to monitor the phenotypic and functional signatures of HCV-specific T cells during acute HCV infection with different infection outcomes and during early IFN therapy. We demonstrate that spontaneous resolution correlates with the early development of polyfunctional (IFN-gamma- and IL-2-producing and CD107a(+)) virus-specific CD8(+) T cells. These polyfunctional T cells are distinguished by the expression of CD127 and Bcl-2 and represent a transitional memory T-cell subset that exhibits the phenotypic and functional signatures of both central and effector memory T cells. In contrast, HCV-specific CD8(+) T cells in acute infections evolving to chronicity expressed low levels of CD127 and Bcl-2, exhibited diminished proliferation and cytokine production, and eventually disappeared from the periphery. Early therapeutic intervention with pegylated IFN-alpha rescued polyfunctional memory T cells expressing high levels of CD127 and Bcl-2. These cells were detectable for up to 1 year following discontinuation of therapy. Our results suggest that the polyfunctionality of HCV-specific T cells can be predictive of the outcome of acute HCV infection and that early therapeutic intervention can reconstitute the pool of long-lived polyfunctional memory T cells.

Indexed as

Hepatitis CInterferon-alphaAdultAmino Acid SequenceCD8-Positive T-LymphocytesEpitopesFemaleHepacivirusHumansImmunologic MemoryInterleukin-7 Receptor alpha SubunitLymphocyte ActivationMaleMiddle AgedMolecular Sequence DataPhenotypeEpitopesInterferon-alphaInterleukin-7 Receptor alpha SubunitProto-Oncogene Proteins c-bcl-2

Identifiers

PMID18667516
PMCPMC2566289
OpenAlexW2119695991

What OpenQuestion holds

Textmetadata
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.