Evidence map›Paper›PMID 34737186›Full record

ArticleDiabetes2022

Regulatory T Cells Control Effector T Cell Inflammation in Human Prediabetes.

Rui Liu, Gabriella H Pugh, Erin Tevonian, Katherine Thompson, Douglas A Lauffenburger, Philip A Kern, Barbara S Nikolajczyk

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

16 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Observational
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. CD36 and Its Role in Regulating the Tumor Microenvironment.Current oncology (Toronto, Ont.) · 2022
    Review
  14. Article
  15. Article
  16. Article
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

7 authors at 2 institutions in 1 country.

Rui LiuDepartment of Pharmaceutical Sciences, University of Kentucky, Lexington, KY.
Gabriella H PughDepartment of Microbiology, Immunology and Molecular Genetics, University of Kentucky, Lexington, KY.
Erin TevonianDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA.
Katherine ThompsonDr. Bing Zhang Department of Statistics, University of Kentucky, Lexington, KY.
Douglas A LauffenburgerDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA.
Philip A KernDepartment of Medicine, University of Kentucky, Lexington, KY.
Barbara S NikolajczykDepartment of Pharmaceutical Sciences, University of Kentucky, Lexington, KY.ORCID 0000-0001-5647-5740
University of Kentucky · USMassachusetts Institute of Technology · US

Funding

University of Kentucky Markey Cancer Center Support Grant ECIA SupplementP30CA177558 · NCI · UNIVERSITY OF KENTUCKY · PI KATHLEEN L. O'CONNOR · 2013 to 2026
$38.3M
Kentucky Center for Clinical and Translational ScienceUL1TR001998 · NCATS · UNIVERSITY OF KENTUCKY · PI HARTMANN, KATHERINE E, KERN, PHILIP A · 2016 to 2025
$34.2M
NRSA Training CoreTL1TR001997 · NCATS · UNIVERSITY OF KENTUCKY · PI PENDERGAST, JULIE S, STOOPS, WILLIAM WALTON · 2016 to 2025
$4.2M
Inflammation in human obesity and type 2 diabetesR01DK108056 · NIDDK · UNIVERSITY OF KENTUCKY · PI LAUFFENBURGER, DOUGLAS A, NIKOLAJCZYK, BARBARA · 2016 to 2019
$2.6M
NCATS NIH HHS TL1 TR001997NCATS NIH HHS UL1 TR001998NCI NIH HHS P30 CA177558NIDDK NIH HHS R01 DK108056
6 · The paper itself

Abstract

A disparate array of plasma/serum markers provides evidence for chronic inflammation in human prediabetes, a condition that is most closely replicated by standard mouse models of obesity and metaflammation. These remain largely nonactionable and contrast with our rich understanding of inflammation in human type 2 diabetes. New data show that inflammatory profiles produced by CD4+ T cells define human prediabetes as a unique inflammatory state. Regulatory T cells (Treg) control mitochondrial function and cytokine production by CD4+ effector T cells (Teff) in prediabetes and type 2 diabetes by supporting T helper (Th)17 or Th1 cytokine production, respectively. These data suggest that Treg control of Teff metabolism regulates inflammation differentially in prediabetes compared with type 2 diabetes. Queries of genes that impact mitochondrial function or pathways leading to transcription of lipid metabolism genes identified the fatty acid importer CD36 as highly expressed in Treg but not Teff from subjects with prediabetes. Pharmacological blockade of CD36 in Treg from subjects with prediabetes decreased Teff production of the Th17 cytokines that differentiate overall prediabetes inflammation. We conclude that Treg control CD4+ T cell cytokine profiles through mechanisms determined, at least in part, by host metabolic status. Furthermore, Treg CD36 uniquely promotes Th17 cytokine production by Teff in prediabetes.

Indexed as

CD4-Positive T-LymphocytesCells, CulturedCohort StudiesCytokinesDiabetes Mellitus, Type 2HumansInflammationObesityPrediabetic StateTh17 CellsT-Lymphocytes, RegulatoryTranscriptomeCytokines

Identifiers

PMID34737186
PMCPMC8914282
OpenAlexW3210243855

What OpenQuestion holds

Textmetadata
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.