Evidence map›Paper›PMID 34905514›Full record

ArticleJCI insight2022

Peripheral blood iNKT cell activation correlates with liver damage during acute hepatitis C.

Tina Senff, Christopher Menne, Christine Cosmovici, Lia Laura Lewis-Ximenez, Jasneet Aneja, Ruth Broering, Arthur Y Kim, Astrid M Westendorf, Ulf Dittmer, Norbert Scherbaum and 2 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Innate immunity and early liver inflammation.Frontiers in immunology · 2023
    Review
  8. 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

12 authors at 5 institutions in 3 countries.

Tina SenffInstitute of Virology, University Hospital Düsseldorf, Heinrich Heine University Düsseldorf, Medical Faculty, Düsseldorf, Germany.
Christopher MenneInstitute of Virology, University Hospital Düsseldorf, Heinrich Heine University Düsseldorf, Medical Faculty, Düsseldorf, Germany.
Christine CosmoviciInstitute of Virology, University Hospital Düsseldorf, Heinrich Heine University Düsseldorf, Medical Faculty, Düsseldorf, Germany.
Lia Laura Lewis-XimenezLaboratory of Viral Hepatitis, Oswaldo Cruz Institute, FIOCRUZ, Rio de Janeiro, Brazil.
Jasneet AnejaGastrointestinal Unit, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Ruth BroeringDepartment of Gastroenterology and Hepatology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
Arthur Y KimDivision of Infectious Diseases, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Astrid M WestendorfInstitute of Medical Microbiology and.
Ulf DittmerInstitute for Virology, University Hospital Essen, University of Duisburg-Essen, Germany.
Norbert ScherbaumLVR-Hospital Essen, Department of Addictive Behaviour and Addiction Medicine, Medical Faculty, University of Duisburg-Essen, Essen, Germany.
Georg M LauerGastrointestinal Unit, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Jörg TimmInstitute of Virology, University Hospital Düsseldorf, Heinrich Heine University Düsseldorf, Medical Faculty, Düsseldorf, Germany.
Düsseldorf University Hospital · DEUniversity of Duisburg-Essen · DEHarvard University · USFundação Oswaldo Cruz · BRMassachusetts General Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Invariant NK T (iNKT) cells are implicated in viral clearance; however, their role in hepatitis C virus (HCV) infection remains controversial. Here, iNKT cells were studied during different stages of HCV infection. iNKT cells from patients with acute HCV infection and people who inject drugs (PWID) with chronic or spontaneously resolved HCV infection were characterized by flow cytometry. In a longitudinal analysis during acute HCV infection, frequencies of activated CD38+ iNKT cells reproducibly declined in spontaneously resolving patients, whereas they were persistently elevated in patients progressing to chronic infection. During the first year of infection, the frequency of activated CD38+ or CD69+ iNKT cells strongly correlated with alanine transaminase levels with particularly pronounced correlations in spontaneously resolving patients. Increased frequencies of activated iNKT cells in chronic HCV infection were confirmed in cross-sectional analyses of PWID with chronic or spontaneously resolved HCV infection; however, no apparent functional differences were observed with various stimulation protocols. Our data suggest that iNKT cells are activated during acute hepatitis C and that activation is sustained in chronic infection. The correlation between the frequency of activated iNKT cells and alanine transaminase may point toward a role of iNKT cells in liver damage.

Indexed as

HepacivirusHepatitis CNatural Killer T-CellsAcute DiseaseADP-ribosyl Cyclase 1Alanine TransaminaseAntigens, CDAntigens, Differentiation, T-LymphocyteCD69 AntigensCross-Sectional StudiesHumansLectins, C-TypeLymphocyte ActivationPersistent InfectionRemission, SpontaneousViral LoadADP-ribosyl Cyclase 1Alanine TransaminaseAntigens, CDAntigens, Differentiation, T-LymphocyteCD69 AntigensLectins, C-TypeHepatitisImmunologyVirology

Identifiers

PMID34905514
PMCPMC8855829
OpenAlexW4200343384

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.