Evidence map›Paper›PMID 28267900›Full record

ArticleJournal of viral hepatitis2017

Augmentation of hepatitis C virus-specific immunity and sustained virologic response.

S Shrivastava, E Wilson, B Poonia, L Tang, A Osinusi, A Kohli, S Kottilil

Open access · greenAbstract readControlled Clinical Trial
In one paragraph

Article in Journal of viral hepatitis, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Peripheral PD-1Frontiers in immunology · 2019
    Trial
  5. Trial
  6. Hepatitis C Eradication Improves Oncologic and Clinical Outcomes in Patients Treated With Atezolizumab Plus Bevacizumab.Liver international : official journal of the International Association for the Study of the Liver · 2025
    Article
  7. Article
  8. Article
  9. Lymphocyte Landscape after ChronicInternational journal of molecular sciences · 2020
    Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. 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

7 authors at 3 institutions in 1 country.

S ShrivastavaInstitute of Human Virology, University of Maryland School of Medicine, Baltimore, MD, USA.ORCID 0000-0001-6276-0791
E WilsonInstitute of Human Virology, University of Maryland School of Medicine, Baltimore, MD, USA.
B PooniaInstitute of Human Virology, University of Maryland School of Medicine, Baltimore, MD, USA.
L TangInstitute of Human Virology, University of Maryland School of Medicine, Baltimore, MD, USA.
A OsinusiGilead Sciences Inc., Foster City, CA, USA.
A KohliCreighton University School of Medicine, St Joseph's Hospital, Phoenix, AZ, USA.
S KottililInstitute of Human Virology, University of Maryland School of Medicine, Baltimore, MD, USA.
University of Maryland, Baltimore · USCreighton University · USGilead Sciences (United States) · US

Funding

DC Partnership for HIV/AIDS Progress (DC PFAP)ZIACL009010 · CLC · CLINICAL CENTER · PI MASUR, HENRY · 2010 to 2025
$0k
Intramural NIH HHS ZIA CL009010
6 · The paper itself

Abstract

Treatment for chronic hepatitis C virus (HCV) infection has rapidly evolved into interferon-free directly acting antiviral regimens (DAA) that result in high sustained virologic response. DAAs primarily work by suppressing HCV replication and rely less on the immune system than interferon-based therapies. However, it is unclear whether the immune system recovers with suppression of HCV replication and contributes to HCV clearance with DAA therapy. We previously demonstrated HCV clearance is associated with increased HCV-specific immunity in CHCV-GT-1-infected patients during treatment with sofosbuvir (SOF)+ribavirin (RBV). Here, we aimed to analyse changes in HCV-specific immunological responses associated with viral clearance with combination DAA therapy of SOF+ledipasvir (LDV) for 12 weeks in CHCV-GT1 (N=14) patients who relapsed without augmentation of HCV-specific immunity during treatment with SOF+RBV. Phenotypic and functional changes within the T-cell compartment of PBMCs pre- and post-treatment were analysed. Retreatment of relapsers with LDV/SOF resulted in all patients attaining SVR

Indexed as

Immunity, CellularSustained Virologic ResponseAgedAntiviral AgentsFemaleHepacivirusHepatitis C, ChronicHumansInterferon-gammaMaleMiddle AgedT-LymphocytesTreatment OutcomeAntiviral AgentsInterferon-gammaantiviral therapycellular immunityhepatitis Cimmune response

Identifiers

PMID28267900
PMCPMC10836410
OpenAlexW2593802464

What OpenQuestion holds

Textmetadata
LicenceTDM
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.