Evidence map›Paper›PMID 15962289›Full record

ArticleHepatology (Baltimore, Md.)2005

Comprehensive analyses of CD8+ T cell responses during longitudinal study of acute human hepatitis C.

Andrea L Cox, Timothy Mosbruger, Georg M Lauer, Drew Pardoll, David L Thomas, Stuart C Ray

Open access · greenAbstract read
In one paragraph

Article in Hepatology (Baltimore, Md.), 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 121 papers.

0numbers the graph read from it
0cells of the map it votes in
121citing papers in PubMed
10.1field-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

121 citing papers in PubMed, 234 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Biomarkers in Detection of Hepatitis C Virus Infection.Pathogens (Basel, Switzerland) · 2024
    Review
  10. Article
  11. Frontiers in microbiology · 2024
    Article
  12. Article
  13. Immunological Monitoring in Hepatitis C Virus Controlled Human Infection Model.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2023
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. CD8Frontiers in immunology · 2022
    Article
  19. Review
  20. Review

61 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

6 authors at 2 institutions in 1 country.

Andrea L CoxDepartment of Medicine, Johns Hopkins Medical Institutions, Baltimore, MD 21231, USA.
Timothy Mosbruger
Georg M Lauer
Drew Pardoll
David L Thomas
Stuart C Ray
Johns Hopkins University · USMassachusetts General Hospital · US

Funding

Virus-Host Interactions in Hepatitis C Virus (HCV) InfectionsU19AI040035 · NIAID · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI LANFORD, ROBERT E · 1996 to 2009
$12.0M
HIV BEHAVIORS IN INJECTING AND NONINJECTING DRUG USERSR01DA011880 · NIDA · JOHNS HOPKINS UNIVERSITY · PI SHERMAN, SUSAN GAIL · 1998 to 2003
$1.3M
SEQUENCE SELECTION AND PERSISTENCE OF HEPATITIS CR01DK057998 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI RAY, STUART C · 1999 to 2003
$1.1M
NIAID NIH HHS N01 AI040035NIAID NIH HHS U19 AI040035NIAID NIH HHS U19 AI40035NIDA NIH HHS K08 DA11880NIDDK NIH HHS R01 DK057998NIDDK NIH HHS R01 DK57998
6 · The paper itself

Abstract

We comprehensively studied the cellular immune response during acute human hepatitis C virus (HCV) infection by monthly prospective sampling of persons at high risk of infection. In 19 of 23 subjects, interferon-gamma-secreting T cells specific for 1 or more peptides spanning the entire HCV polyprotein were detected 1 to 3 months after infection. The median time to development of interferon gamma responses to HCV peptides was 33 days (range, 29-50 days), and these responses peaked between 180 and 360 days. Nineteen subjects had sufficient follow-up to determine outcome, with 15 (79%) developing persistent viremia and 4 (21%) clearing viremia spontaneously. Of those with progression to chronic infection and detectable T cell responses, all lost recognition of one or more antigens recognized during acute infection, and the median reduction in the magnitude of responses was 85%. Most significantly, despite ongoing viremia, those who had persistent infection did not develop new epitope specificities after the first 6 months of infection. In conclusion, in most individuals, the CD8+ T cell responses generated early in HCV infection decline in peripheral blood and are not replaced with new responses. Supplementary material for this article can be found on the HEPATOLOGY website (http://www.interscience.wiley.com/jpages/0270-9139/suppmat/index.html).

Indexed as

Acute DiseaseAdolescentAdultCD8-Positive T-LymphocytesFemaleHepatitis CHumansMaleProspective Studies

Identifiers

PMID15962289
PMCPMC2759395
OpenAlexW2148099428

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.