Evidence map›Paper›PMID 31883840›Full record

ArticleCell metabolism2020

Mitochondrial Integrity Regulated by Lipid Metabolism Is a Cell-Intrinsic Checkpoint for Treg Suppressive Function.

Cameron S Field, Francesc Baixauli, Ryan L Kyle, Daniel J Puleston, Alanna M Cameron, David E Sanin, Keli L Hippen, Michael Loschi, Govindarajan Thangavelu, Mauro Corrado and 5 more

Open access · greenAbstract read
In one paragraph

Article in Cell metabolism, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 265 papers.

0numbers the graph read from it
0cells of the map it votes in
265citing papers in PubMed
15.1field-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

265 citing papers in PubMed, 406 citations in OpenAlex.

  1. Review
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  7. Article
  8. cGAS: bridging immunity and metabolic regulation.Journal of molecular cell biology · 2026
    Review
  9. Adaptive resistance in cancer immunotherapy.Cellular & molecular immunology · 2026
    Review
  10. Article
  11. Review
  12. Review
  13. Review
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  15. Article
  16. Article
  17. Review
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  20. Review

205 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

15 authors at 4 institutions in 3 countries.

Cameron S FieldMax Planck Institute for Immunobiology and Epigenetics, 79108 Freiburg, Germany.
Francesc BaixauliMax Planck Institute for Immunobiology and Epigenetics, 79108 Freiburg, Germany.
Ryan L KyleMax Planck Institute for Immunobiology and Epigenetics, 79108 Freiburg, Germany.
Daniel J PulestonMax Planck Institute for Immunobiology and Epigenetics, 79108 Freiburg, Germany; The Kennedy Institute of Rheumatology, University of Oxford, Oxford, OX3 7FY, UK.
Alanna M CameronMax Planck Institute for Immunobiology and Epigenetics, 79108 Freiburg, Germany.
David E SaninMax Planck Institute for Immunobiology and Epigenetics, 79108 Freiburg, Germany.
Keli L HippenDivision of Blood and Marrow Transplantation, Department of Pediatrics, Masonic Cancer Center, University of Minnesota, Minneapolis, MN, USA.
Michael LoschiDivision of Blood and Marrow Transplantation, Department of Pediatrics, Masonic Cancer Center, University of Minnesota, Minneapolis, MN, USA.
Govindarajan ThangaveluDivision of Blood and Marrow Transplantation, Department of Pediatrics, Masonic Cancer Center, University of Minnesota, Minneapolis, MN, USA.
Mauro CorradoMax Planck Institute for Immunobiology and Epigenetics, 79108 Freiburg, Germany.
Joy Edwards-HicksMax Planck Institute for Immunobiology and Epigenetics, 79108 Freiburg, Germany.
Katarzyna M GrzesMax Planck Institute for Immunobiology and Epigenetics, 79108 Freiburg, Germany.
Edward J PearceMax Planck Institute for Immunobiology and Epigenetics, 79108 Freiburg, Germany; Faculty of Biology, University of Freiburg, 79104 Freiburg, Germany.
Bruce R BlazarDivision of Blood and Marrow Transplantation, Department of Pediatrics, Masonic Cancer Center, University of Minnesota, Minneapolis, MN, USA.
Erika L PearceMax Planck Institute for Immunobiology and Epigenetics, 79108 Freiburg, Germany. Electronic address: pearce@ie-freiburg.mpg.de.
Max Planck Institute of Immunobiology and Epigenetics · DEUniversity of Minnesota Medical Center · USUniversity of Freiburg · DEUniversity of Oxford · GB

Funding

Trial Design and Biostatistical Support CoreP01CA065493 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Mark J Osborn · 1995 to 2026
$48.2M
Transgenic/KnockoutP01AI056299 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI SHARPE, ARLENE H. · 2003 to 2023
$42.5M
Project 3: Humoral Targets and B Cell Biology in Chronic Graft-vs.-Host DiseaseP01CA142106 · NCI · DANA-FARBER CANCER INST · PI CUTLER, COREY S · 2009 to 2019
$17.5M
Enhancing Treg Therapeutic Efficacy in GVHDR01HL118979 · NHLBI · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R, HIPPEN, KELI L · 2014 to 2025
$6.7M
T-CELL TARGETING FOR GVHDR01HL056067 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BLAZAR, BRUCE R · 1995 to 2022
$5.4M
In Vivo Prevention of Murine GVHDR37AI034495 · NIAID · UNIVERSITY OF MINNESOTA · PI Bruce R Blazar · 2017 to 2026
$5.4M
Nongenotoxic conditioning for gene therapy and allogeneic transplantation in Fanconi anemiaR01HL147324 · NHLBI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Bruce R Blazar, HANS-PETER KIEM · 2020 to 2026
$4.1M
Dendritic Cell Function in SchistosomiasisR01AI053825 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI PEARCE, EDWARD J. · 2002 to 2010
$3.4M
MACROPHAGE FATTY ACID METABOLISM IN IMMUNITY TO HELMINTHSR01AI110481 · NIAID · WASHINGTON UNIVERSITY · PI PEARCE, EDWARD J. · 2015 to 2019
$1.5M
TUMOR-IMPOSED GLUCOSE RESTRICTIONS ON T CELLS DAMPEN IMMUNITYR01CA181125 · NCI · WASHINGTON UNIVERSITY · PI PEARCE, ERIKA L · 2014 to 2017
$989k
NCI NIH HHS P01 CA065493NCI NIH HHS P01 CA142106NCI NIH HHS R01 CA181125NHLBI NIH HHS R01 HL056067NHLBI NIH HHS R01 HL118979NHLBI NIH HHS R01 HL147324NIAID NIH HHS P01 AI056299NIAID NIH HHS R01 AI053825NIAID NIH HHS R01 AI110481NIAID NIH HHS R37 AI034495Wellcome Trust 201330/Z/16/Z
6 · The paper itself

Abstract

Regulatory T cells (Tregs) subdue immune responses. Central to Treg activation are changes in lipid metabolism that support their survival and function. Fatty acid binding proteins (FABPs) are a family of lipid chaperones required to facilitate uptake and intracellular lipid trafficking. One family member, FABP5, is expressed in T cells, but its function remains unclear. We show that in Tregs, genetic or pharmacologic inhibition of FABP5 function causes mitochondrial changes underscored by decreased OXPHOS, impaired lipid metabolism, and loss of cristae structure. FABP5 inhibition in Tregs triggers mtDNA release and consequent cGAS-STING-dependent type I IFN signaling, which induces heightened production of the regulatory cytokine IL-10 and promotes Treg suppressive activity. We find evidence of this pathway, along with correlative mitochondrial changes in tumor infiltrating Tregs, which may underlie enhanced immunosuppression in the tumor microenvironment. Together, our data reveal that FABP5 is a gatekeeper of mitochondrial integrity that modulates Treg function.

Indexed as

Lipid MetabolismAnimalsCell Line, TumorDNA, MitochondrialFatty Acid-Binding ProteinsHumansInterferon Type IInterleukin-10MiceMice, Inbred C57BLMice, KnockoutMitochondriaT-Lymphocytes, RegulatoryDNA, MitochondrialFABP5 protein, humanFatty Acid-Binding ProteinsIL10 protein, humanInterferon Type IInterleukin-10cGAS-STINGFABP5IL-10immunometabolismlipidsmtDNAsuppressionTregtumortype I IFN

Identifiers

PMID31883840
PMCPMC7001036
OpenAlexW2997656567

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.