Evidence map›Paper›PMID 25001241›Full record

ArticleImmunity2014

Memory CD8(+) T cells use cell-intrinsic lipolysis to support the metabolic programming necessary for development.

David O'Sullivan, Gerritje J W van der Windt, Stanley Ching-Cheng Huang, Jonathan D Curtis, Chih-Hao Chang, Michael D Buck, Jing Qiu, Amber M Smith, Wing Y Lam, Lisa M DiPlato and 4 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Immunity, 2014. 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 510 papers.

0numbers the graph read from it
0cells of the map it votes in
510citing papers in PubMed
51.3field-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

510 citing papers in PubMed, 766 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Advances in Lipid Metabolism Reprogramming in Hepatocellular Carcinoma.Journal of clinical and translational hepatology · 2026
    Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. CD8Science China. Life sciences · 2026
    Review
  12. A new twist in metabolic T cell exhaustion.Immunometabolism (Cobham, Surrey) · 2026
    Article
  13. Article
  14. Review
  15. Lipid metabolism in homeostasis and disease.Signal transduction and targeted therapy · 2026
    Review
  16. FASN-mediated metabolic reprogramming drives CD4Arthritis research & therapy · 2026
    Article
  17. Review
  18. Review
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 2 institutions in 1 country.

David O'SullivanDepartment of Pathology & Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Gerritje J W van der WindtDepartment of Pathology & Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Stanley Ching-Cheng HuangDepartment of Pathology & Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Jonathan D CurtisDepartment of Pathology & Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Chih-Hao ChangDepartment of Pathology & Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Michael D BuckDepartment of Pathology & Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Jing QiuDepartment of Pathology & Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Amber M SmithDepartment of Pathology & Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Wing Y LamDepartment of Pathology & Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Lisa M DiPlatoThe Institute for Diabetes, Obesity, and Metabolism, University of Pennsylvania, Philadelphia, PA 19104, USA.
Fong-Fu HsuMass Spectrometry Resource, Division of Endocrinology, Diabetes, Metabolism, and Lipid Research, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Morris J BirnbaumThe Institute for Diabetes, Obesity, and Metabolism, University of Pennsylvania, Philadelphia, PA 19104, USA.
Edward J PearceDepartment of Pathology & Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Erika L PearceDepartment of Pathology & Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: erikapearce@path.wustl.edu.
Washington University in St. Louis · USUniversity of Pennsylvania · US

Funding

Washington University Nutrition Obesity Research CenterP30DK056341 · NIDDK · WASHINGTON UNIVERSITY · PI Brian N Finck · 1999 to 2026
$30.2M
WU P&FP30DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI Jennifer Lynn Powers Carson · 2013 to 2026
$27.1M
TrainingP41GM103422 · NIGMS · WASHINGTON UNIVERSITY · PI YARASHESKI, KEVIN E · 2012 to 2019
$12.0M
Metabolic Regulation of CD8 T Cell Memory DevelopmentR01AI091965 · NIAID · WASHINGTON UNIVERSITY · PI PEARCE, ERIKA L · 2011 to 2015
$1.9M
MANIPULATING DENDRITIC CELL METABOLISM TO PROMOTE CANCER IMMUNITYR01CA164062 · NCI · WASHINGTON UNIVERSITY · PI PEARCE, EDWARD J. · 2012 to 2016
$1.7M
Targeting mTOR for Immunity to CancerR21CA158823 · NCI · WASHINGTON UNIVERSITY · PI PEARCE, ERIKA L · 2011 to 2012
$411k
NCI NIH HHS CA158823NCI NIH HHS CA164062NCI NIH HHS R01 CA164062NCI NIH HHS R21 CA158823NIAID NIH HHS AI091965NIAID NIH HHS R01 AI091965NIDDK NIH HHS P30 DK020579NIDDK NIH HHS P30 DK056341NIGMS NIH HHS P41 GM103422
6 · The paper itself

Abstract

Generation of CD8(+) memory T cells requires metabolic reprogramming that is characterized by enhanced mitochondrial fatty-acid oxidation (FAO). However, where the fatty acids (FA) that fuel this process come from remains unclear. While CD8(+) memory T cells engage FAO to a greater extent, we found that they acquired substantially fewer long-chain FA from their external environment than CD8(+) effector T (Teff) cells. Rather than using extracellular FA directly, memory T cells used extracellular glucose to support FAO and oxidative phosphorylation (OXPHOS), suggesting that lipids must be synthesized to generate the substrates needed for FAO. We have demonstrated that memory T cells rely on cell intrinsic expression of the lysosomal hydrolase LAL (lysosomal acid lipase) to mobilize FA for FAO and memory T cell development. Our observations link LAL to metabolic reprogramming in lymphocytes and show that cell intrinsic lipolysis is deterministic for memory T cell fate.

Indexed as

4-ButyrolactoneAdoptive TransferAnimalsCD8-Positive T-LymphocytesCell ProliferationCells, CulturedCell SurvivalFatty AcidsFatty Acid SynthasesGlucoseImmunologic MemoryInterleukin-15Interleukin-2LipolysisLymphocyte ActivationMice4-Butyrolactone4-methylene-2-octyl-5-oxofuran-3-carboxylic acidATP-citrate lyase kinaseFatty AcidsFatty Acid SynthasesGlucoseInterleukin-15Interleukin-2OxygenProtein KinasesRNA, Small InterferingSterol Esterase

Identifiers

PMID25001241
PMCPMC4120664
OpenAlexW2131199230

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.