Evidence map›Paper›PMID 26038456›Full record

ReviewEmerging microbes & infections2013

T-cell responses in hepatitis B and C virus infection: similarities and differences.

Julia Schmidt, Hubert E Blum, Robert Thimme

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in Emerging microbes & infections, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02690103 (Clinical Study of a Biological Response Modifier), which is not on this map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
3.4field-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.

NCT02690103 phase2completednot on this map

Clinical Study of a Biological Response Modifier (Arabinoxylan Rice Bran/MGN-3/Biobran) With Interferon-Alpha for the Treatment of Hepatitis C Infection

TypeinterventionalSponsorCairo UniversityRan2012 to 2015Enrolled37ConditionsHepatitis C, ChronicArmspegylated IFN, Biobran, Ribavirin
3 · Its place in the literature

Who cites it

46 citing papers in PubMed, 81 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Clinical andInfectious disorders drug targets · 2025
    Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. The Liver-Immunity Nexus and Cancer Immunotherapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. A quantitative systems pharmacology model for acute viral hepatitis B.Computational and structural biotechnology journal · 2021
    Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article
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

3 authors at 1 institution in 1 country.

Julia SchmidtDepartment of Medicine II, University Hospital Freiburg , D-79106 Freiburg, Germany.
Hubert E BlumDepartment of Medicine II, University Hospital Freiburg , D-79106 Freiburg, Germany.
Robert ThimmeDepartment of Medicine II, University Hospital Freiburg , D-79106 Freiburg, Germany.
University Medical Center Freiburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic hepatitis B virus (HBV) and hepatitis C virus (HCV) infection are global health problems affecting 600 million people worldwide. Indeed, HBV and HCV are hepatotropic viruses that can cause acute and chronic liver disease progressing to liver cirrhosis and even hepatocellular carcinoma. Furthermore, co-infections of HBV and HCV with HIV are emerging worldwide. These co-infections are even more likely to develop persistent infection and are difficult to treat. There is growing evidence that virus-specific CD4(+) and CD8(+) T-cell responses play a central role in the outcome and pathogenesis of HBV and HCV infection. While virus-specific T-cell responses are able to successfully clear the virus in a subpopulation of patients, failure of these T-cell responses is associated with the development of viral persistence. In this review article, we will discuss similarities and differences in HBV- and HCV-specific T-cell responses that are central in determining viral clearance, persistence and liver disease.

Indexed as

adaptive immunityCD4+ and CD8+ T cellshepatitis B virushepatitis C virus

Identifiers

PMID26038456
PMCPMC3630955
OpenAlexW2004597368

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.