Evidence map›Paper›PMID 28073373›Full record

ReviewCell communication and signaling : CCS2017

T cell exhaustion: from pathophysiological basics to tumor immunotherapy.

Kemal Catakovic, Eckhard Klieser, Daniel Neureiter, Roland Geisberger

Abstract readReview
In one paragraph

Review in Cell communication and signaling : CCS, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 114 papers.

0numbers the graph read from it
0cells of the map it votes in
114citing papers in PubMed
–field-weighted citation impact
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

114 citing papers in PubMed.

  1. Trial
  2. Maintenance Pembrolizumab Therapy in Patients with Metastatic HER2-negative Breast Cancer with Prior Response to Chemotherapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Trial
  3. Trial
  4. Trial
  5. Article
  6. Article
  7. T cell exhaustion inParasite epidemiology and control · 2026
    Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Characterization and effective expansion of CD4Molecular therapy. Methods & clinical development · 2025
    Article
  17. Review
  18. Review
  19. Article
  20. VISTAFrontiers in immunology · 2025
    Article

54 more citing papers are in PubMed but not listed here.

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

4 authors.

Kemal CatakovicLaboratory for Immunological and Molecular Cancer Research, Department of Internal Medicine III with Haematology, Medical Oncology, Haemostaseology, Infectiology and Rheumatology, Oncologic Center, Paracelsus Medical University, Müllner Hauptstrasse 48, Salzburg, 5020, Austria.
Eckhard KlieserSalzburg Cancer Research Institute, Salzburg, Austria.
Daniel NeureiterSalzburg Cancer Research Institute, Salzburg, Austria.
Roland GeisbergerLaboratory for Immunological and Molecular Cancer Research, Department of Internal Medicine III with Haematology, Medical Oncology, Haemostaseology, Infectiology and Rheumatology, Oncologic Center, Paracelsus Medical University, Müllner Hauptstrasse 48, Salzburg, 5020, Austria. r.geisberger@salk.at.ORCID http://orcid.org/0000-0002-0131-2191

Funding

Austrian Science Fund FWF P 28201
6 · The paper itself

Abstract

The immune system is capable of distinguishing between danger- and non-danger signals, thus inducing either an appropriate immune response against pathogens and cancer or inducing self-tolerance to avoid autoimmunity and immunopathology. One of the mechanisms that have evolved to prevent destruction by the immune system, is to functionally silence effector T cells, termed T cell exhaustion, which is also exploited by viruses and cancers for immune escape In this review, we discuss some of the phenotypic markers associated with T cell exhaustion and we summarize current strategies to reinvigorate exhausted T cells by blocking these surface marker using monoclonal antibodies.

Indexed as

ImmunotherapyAnimalsClinical Trials as TopicHumansModels, BiologicalNeoplasmsReceptors, ImmunologicT-LymphocytesReceptors, ImmunologicCancerImmunotherapyPD-1PD-L1T cell exhaustion

Identifiers

PMID28073373
PMCPMC5225559

What OpenQuestion holds

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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.