Evidence map›Paper›PMID 27002844›Full record

ArticleNature immunology2016

Emerging concepts of T cell metabolism as a target of immunotherapy.

Chih-Hao Chang, Erika L Pearce

Abstract read
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. Cited by 212 papers.

0numbers the graph read from it
0cells of the map it votes in
212citing papers in PubMed
20.7field-weighted citation impact, top 1% 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

212 citing papers in PubMed, 326 citations in OpenAlex.

  1. Review
  2. Review
  3. Coixenolide Enhances Antitumor Immunity of Cytotoxic CD8Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  4. Article
  5. Review
  6. Pharmacologic DPP-4 inhibition promotes CD8bioRxiv : the preprint server for biology · 2026
    Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Neoantigen mRNA vaccines and AHuman vaccines & immunotherapeutics · 2025
    Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. Review

152 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

2 authors at 2 institutions in 2 countries.

Chih-Hao ChangDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.ORCID http://orcid.org/0000-0002-0139-7439
Erika L PearceDepartment of Immunometabolism, Max Planck Institute of Immunobiology and Epigenetics, Freiburg, Germany.
Max Planck Institute of Immunobiology and Epigenetics · DEWashington University in St. Louis · US

Funding

Metabolic Regulation of CD8 T Cell Memory DevelopmentR01AI091965 · NIAID · WASHINGTON UNIVERSITY · PI PEARCE, ERIKA L · 2011 to 2015
$1.9M
TUMOR-IMPOSED GLUCOSE RESTRICTIONS ON T CELLS DAMPEN IMMUNITYR01CA181125 · NCI · WASHINGTON UNIVERSITY · PI PEARCE, ERIKA L · 2014 to 2017
$989k
NCI NIH HHS R01 CA181125NCI NIH HHS R01CA181125NIAID NIH HHS R01 AI091965
6 · The paper itself

Abstract

T cells have a pivotal protective role in defense against infection and cancer but also are instrumental in the development of many autoimmune diseases. The regulation of nutrient uptake and utilization in T cells is critically important for the control of their differentiation, and manipulating metabolic pathways in these cells can alter their function and longevity. While the importance of T cell metabolic remodeling in different physiological settings is not fully understood, there is a growing realization that inappropriate metabolic remodeling underlies many aberrant immune responses and that manipulating cellular metabolism can beneficially enhance or temper immunity. Here we comment on the basic metabolic pathways in T cells, followed by a discussion on up-to-date findings about the relationship between metabolism and T cell function and longevity. Furthermore, we expand on potential approaches and applications in which T cells might be manipulated by the reprogramming of metabolic pathways for therapeutic purposes.

Indexed as

Immunotherapy, AdoptiveAMP-Activated Protein KinasesAnimalsAutoimmune DiseasesCell DifferentiationGlycolysisHumansImmunotherapyMetabolic Networks and PathwaysNeoplasmsOxidative PhosphorylationSignal TransductionT-LymphocytesTOR Serine-Threonine KinasesTumor MicroenvironmentAMP-Activated Protein KinasesTOR Serine-Threonine Kinases

Identifiers

PMID27002844
PMCPMC4990080
OpenAlexW2302941161

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.