Evidence map›Paper›PMID 26950238›Full record

ArticleNature immunology2016

Tumor-necrosis factor impairs CD4(+) T cell-mediated immunological control in chronic viral infection.

Marc Beyer, Zeinab Abdullah, Jens M Chemnitz, Daniela Maisel, Jil Sander, Clara Lehmann, Yasser Thabet, Prashant V Shinde, Lisa Schmidleithner, Maren Köhne and 14 more

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Nature immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

50 citing papers in PubMed, 84 citations in OpenAlex.

  1. Upregulation of TNFR2 Precedes TOX Expression by Exhausted T cells and Restricts Antitumor and Antiviral Immunity.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
  2. Review
  3. A promising advance using oncolytic adenovirus to locally block tumorigenic TNF signaling.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  4. Article
  5. Article
  6. Prostaglandin ENature communications · 2024
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Identification of the novel FOXP3-dependent TFrontiers in immunology · 2023
    Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. CD4 T-Cell Exhaustion: Does It Exist and What Are Its Roles in Cancer?Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Review
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 10 institutions in 2 countries.

Marc BeyerLife and Medical Sciences Bonn, Genomics &Immunoregulation, University of Bonn, Bonn, Germany.ORCID http://orcid.org/0000-0001-9704-148X
Zeinab AbdullahInstitute of Experimental Immunology, University Hospital Bonn, Bonn, Germany.
Jens M ChemnitzDepartment of Internal Medicine I, University Hospital Cologne, Cologne, Germany.
Daniela MaiselDepartment of Internal Medicine I, University Hospital Cologne, Cologne, Germany.
Jil SanderLife and Medical Sciences Bonn, Genomics &Immunoregulation, University of Bonn, Bonn, Germany.
Clara LehmannDepartment of Internal Medicine I, University Hospital Cologne, Cologne, Germany.
Yasser ThabetLife and Medical Sciences Bonn, Genomics &Immunoregulation, University of Bonn, Bonn, Germany.
Prashant V ShindeDepartment of Gastroenterology, Hepatology and Infectious Diseases, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.
Lisa SchmidleithnerLife and Medical Sciences Bonn, Genomics &Immunoregulation, University of Bonn, Bonn, Germany.
Maren KöhneLife and Medical Sciences Bonn, Genomics &Immunoregulation, University of Bonn, Bonn, Germany.
Jonel TrebickaDepartment of Internal Medicine I, University Hospital Bonn, Bonn, Germany.
Robert SchierwagenDepartment of Internal Medicine I, University Hospital Bonn, Bonn, Germany.ORCID http://orcid.org/0000-0002-2195-3666
Andrea HofmannLife and Medical Sciences Bonn, Genomics &Immunoregulation, University of Bonn, Bonn, Germany.
Alexey PopovLife and Medical Sciences Bonn, Genomics &Immunoregulation, University of Bonn, Bonn, Germany.
Karl S LangInstitute of Immunology, Faculty of Medicine, University of Duisburg-Essen, Essen, Germany.
Annette OxeniusInstitute of Microbiology, Swiss Federal Institute of Technology Zürich, Zürich, Switzerland.
Thorsten BuchInstitute of Laboratory Animal Science, University of Zürich, Schlieren, Switzerland.ORCID http://orcid.org/0000-0002-2236-9074
Christian KurtsInstitute of Experimental Immunology, University Hospital Bonn, Bonn, Germany.ORCID http://orcid.org/0000-0002-6620-2401
Mathias HeikenwalderInstitute of Virology, Technische Universität/Helmholtz Zentrum München, München, Germany.
Gerd FätkenheuerDepartment of Internal Medicine I, University Hospital Cologne, Cologne, Germany.
Philipp A LangDepartment of Gastroenterology, Hepatology and Infectious Diseases, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.
Pia HartmannDepartment of Internal Medicine I, University Hospital Cologne, Cologne, Germany.
Percy A KnolleInstitute of Experimental Immunology, University Hospital Bonn, Bonn, Germany.ORCID http://orcid.org/0000-0003-2983-0414
Joachim L SchultzeLife and Medical Sciences Bonn, Genomics &Immunoregulation, University of Bonn, Bonn, Germany.
University of Bonn · DEUniversity Hospital Bonn · DEGerman Center for Infection Research · DEHeinrich Heine University Düsseldorf · DEUniversity Hospital Cologne · DEÉcole Polytechnique Fédérale de Lausanne · CHGerman Cancer Research Center · DEUniversity of Cologne · DEUniversity of Duisburg-Essen · DEUniversity of Zurich · CH

Funding

PHS HHS HHSN272201300006C
6 · The paper itself

Abstract

Persistent viral infections are characterized by the simultaneous presence of chronic inflammation and T cell dysfunction. In prototypic models of chronicity--infection with human immunodeficiency virus (HIV) or lymphocytic choriomeningitis virus (LCMV)--we used transcriptome-based modeling to reveal that CD4(+) T cells were co-exposed not only to multiple inhibitory signals but also to tumor-necrosis factor (TNF). Blockade of TNF during chronic infection with LCMV abrogated the inhibitory gene-expression signature in CD4(+) T cells, including reduced expression of the inhibitory receptor PD-1, and reconstituted virus-specific immunity, which led to control of infection. Preventing signaling via the TNF receptor selectively in T cells sufficed to induce these effects. Targeted immunological interventions to disrupt the TNF-mediated link between chronic inflammation and T cell dysfunction might therefore lead to therapies to overcome persistent viral infection.

Indexed as

AdolescentAdultAgedAnimalsCD4-Positive T-LymphocytesFlow CytometryHEK293 CellsHIVHIV InfectionsHost-Pathogen InteractionsHumansImmunoblottingLymphocytic ChoriomeningitisLymphocytic choriomeningitis virusMice, Inbred C57BLMice, KnockoutProgrammed Cell Death 1 ReceptorReceptors, Tumor Necrosis FactorTumor Necrosis Factor-alpha

Identifiers

PMID26950238
OpenAlexW2296666948

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.