Evidence map›Paper›PMID 37541771›Full record

ArticleGut2023

Enolase represents a metabolic checkpoint controlling the differential exhaustion programmes of hepatitis virus-specific CD8

Frances Winkler, Anna V Hipp, Carlos Ramirez, Bianca Martin, Matteo Villa, Emilia Neuwirt, Oliver Gorka, Jeroen Aerssens, Susanne E Johansson, Nisha Rana and 15 more

Open access · hybridAbstract read
In one paragraph

Article in Gut, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
7.2field-weighted citation impact, top 3% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  3. T cell adaptation in chronic infections and tumors.Cellular & molecular immunology · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

25 authors at 9 institutions in 4 countries.

Frances WinklerClinic for Internal Medicine II, Freiburg University Medical Center, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.
Anna V HippClinic for Internal Medicine II, Freiburg University Medical Center, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.
Carlos RamirezHealth Data Science Unit, Medical Faculty, University of Heidelberg, Heidelberg, Germany.
Bianca MartinClinic for Internal Medicine II, Freiburg University Medical Center, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.
Matteo VillaMax Planck Institute of Immunobiology and Epigenetics, Freiburg im Breisgau, Germany.
Emilia NeuwirtInstitute of Neuropathology, Freiburg University Medical Center, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.
Oliver GorkaInstitute of Neuropathology, Freiburg University Medical Center, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.
Jeroen AerssensTranslational Biomarkers, Infectious Diseases Therapeuic Area, Janssen Pharmaceutica, Beerse, Belgium.
Susanne E JohanssonTranslational Biomarkers, Infectious Diseases Therapeuic Area, Janssen Pharmaceutica, Beerse, Belgium.
Nisha RanaClinic for Internal Medicine II, Freiburg University Medical Center, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.
Sian Llewellyn-LaceyDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff University, Cardiff, UK.
David A PriceDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff University, Cardiff, UK.ORCID 0000-0001-9416-2737
Marcus PanningInstitute of Virology, Freiburg University Medical Center, Faculty of Medicine, University Hospital Freiburg, Freiburg im Breisgau, Germany.
Olaf GroßInstitute of Neuropathology, Freiburg University Medical Center, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.
Erika L PearceThe Bloomberg-Kimmel Institute for Cancer Immunotherapy, Johns Hopkins Medicine Sidney Kimmel Comprehensive Cancer Center, Baltimore, Maryland, USA.
Carl M HermannHealth Data Science Unit, Medical Faculty, University of Heidelberg, Heidelberg, Germany.
Kathrin SchumannInstitute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich (TUM), Munich, Germany.
Luciana HannibalDepartment of General Pediatrics, Laboratory of Clinical Biochemistry and Metabolism, Medical Center-University of Freiburg, Adolescent Medicine and Neonatology, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Christoph Neumann-HaefelinClinic for Internal Medicine II, Freiburg University Medical Center, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.
Tobias BoettlerClinic for Internal Medicine II, Freiburg University Medical Center, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.ORCID 0000-0002-1195-055X
Percy KnolleGerman Center for Infection Research (DZIF), Munich Partner Site, Munich, Germany.
Maike HofmannClinic for Internal Medicine II, Freiburg University Medical Center, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.ORCID 0000-0001-8410-8833
Dirk WohlleberInstitute of Molecular Immunology, Klinikum Rechts der Isar, Technical University of Munich, Munich, Germany.
Robert ThimmeClinic for Internal Medicine II, Freiburg University Medical Center, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.ORCID 0000-0003-1417-4135
Bertram BengschClinic for Internal Medicine II, Freiburg University Medical Center, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany bertram.bengsch@uniklinik-freiburg.de.ORCID 0000-0003-2552-740X
University of Freiburg · DECardiff University · GBHeidelberg University · DEJanssen (Belgium) · BETUM Klinikum · DEBloomberg (United States) · USInstitute of Medical Microbiology and Hygiene · DEMax Planck Institute of Immunobiology and Epigenetics · DEUniversity Medical Center Freiburg · DE

Funding

Wellcome TrustWellcome Trust 100326/Z/12/Z
6 · The paper itself

Abstract

objectiveExhausted T cells with limited effector function are enriched in chronic hepatitis B and C virus (HBV and HCV) infection. Metabolic regulation contributes to exhaustion, but it remains unclear how metabolism relates to different exhaustion states, is impacted by antiviral therapy, and if metabolic checkpoints regulate dysfunction.

designMetabolic state, exhaustion and transcriptome of virus-specific CD8

resultsHBV-specific (core

conclusionMetabolism of HBV-specific and HCV-specific T cells is strongly connected to their exhaustion severity. Our results highlight enolase as metabolic regulator of severely exhausted T cells. They connect differential bioenergetic fitness with distinct exhaustion subtypes and varying liver disease, with implications for therapeutic strategies.

Indexed as

Hepatitis B, ChronicHepatitis CHepatitis C, ChronicAnimalsAntiviral AgentsCD8-Positive T-LymphocytesHepatitis B virusHepatitis VirusesHumansMicePersistent InfectionAntiviral Agentsalpha beta T cellschronic viral hepatitishepatitis Bhepatitis Cimmunology in hepatology

Identifiers

PMID37541771
PMCPMC10511960
OpenAlexW4385574990

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.