Evidence map›Paper›PMID 27910764›Full record

ReviewCritical reviews in immunology2016

Metabolic Regulation of Natural Killer Cell IFN-γ Production.

Annelise Y Mah, Megan A Cooper

Abstract readReview
In one paragraph

Review in Critical reviews in immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 101 papers.

0numbers the graph read from it
0cells of the map it votes in
101citing 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

101 citing papers in PubMed.

  1. Trial
  2. Review
  3. Review
  4. Interleukin-18 armours antitumour immune effectors.Nature reviews. Immunology · 2026
    Review
  5. Article
  6. Review
  7. Article
  8. Article
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  11. Article
  12. Review
  13. Article
  14. Article
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  16. Article
  17. Review
  18. Article
  19. Immunoenhancing Effects of JejuPharmaceuticals (Basel, Switzerland) · 2025
    Article
  20. Article

41 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.

Annelise Y MahDepartment of Pediatrics, Division of Rheumatology, Washington University School of Medicine, St. Louis, MO.
Megan A CooperDepartment of Pediatrics, Division of Rheumatology, Washington University School of Medicine, St. Louis, MO.

Funding

NATIONAL RESEARCH SERVICE AWARD-MEDICAL SCIENTISTT32GM007200 · NIGMS · WASHINGTON UNIVERSITY · PI YOKOYAMA, WAYNE M. · 1985 to 2024
$59.8M
Mechanisms of Innate Immune MemoryK08AI085030 · NIAID · WASHINGTON UNIVERSITY · PI COOPER, MEGAN ANNE · 2010 to 2014
$600k
NIAID NIH HHS K08 AI085030NIGMS NIH HHS T32 GM007200
6 · The paper itself

Abstract

Metabolism is critical for a host of cellular functions and provides a source of intracellular energy. It has been recognized recently that metabolism also regulates differentiation and effector functions of immune cells. Although initial work in this field has focused largely on T lymphocytes, recent studies have demonstrated metabolic control of innate immune cells, including natural killer (NK) cells. Here, we review what is known regarding the metabolic requirements for NK cell activation, focusing on NK cell production of interferon-gamma (IFN-γ). NK cells are innate immune lymphocytes that are poised for rapid activation during the early immune response. Although their basal metabolic rates do not change with short-term activation, they exhibit specific metabolic requirements for activation depending upon the stimulus received. These metabolic requirements for NK cell activation are altered by culturing NK cells with interleukin-15, which increases NK cell metabolic rates at baseline and shifts them toward aerobic glycolysis. We discuss the metabolic pathways important for NK cell production of IFN-γ protein and potential mechanisms whereby metabolism regulates NK cell function.

Indexed as

AnimalsHumansInterferon-gammaKiller Cells, NaturalLymphocytesInterferon-gamma

Identifiers

PMID27910764
PMCPMC5335907

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Registered trials

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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.