Evidence map›Paper›PMID 24222350›Full record

ArticleDiabetes2014

T-cell costimulation protects obesity-induced adipose inflammation and insulin resistance.

Jixin Zhong, Xiaoquan Rao, Zachary Braunstein, Anne Taylor, Vimal Narula, Jeffrey Hazey, Dean Mikami, Bradley Needleman, Jessica Rutsky, Qinghua Sun and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Diabetes, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
5.5field-weighted citation impact, top 4% 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

42 citing papers in PubMed, 68 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Adipose-tissue regulatory T cells are a consortium of subtypes that evolves with age and diet.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  6. Adipose tissue lymphocytes and obesity.The journal of cardiovascular aging · 2024
    Article
  7. Article
  8. Article
  9. Review
  10. Tissue regulatory T cells: regulatory chameleons.Nature reviews. Immunology · 2021
    Review
  11. Review
  12. Article
  13. Review
  14. Adipose Tissue T Regulatory Cells: Implications for Health and Disease.Advances in experimental medicine and biology · 2021
    Article
  15. Article
  16. Review
  17. B Lymphocytes and Adipose Tissue Inflammation.Arteriosclerosis, thrombosis, and vascular biology · 2020
    Review
  18. Article
  19. Article
  20. Inflammation and Immunity: From an Adipocyte's Perspective.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2019
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 1 country.

Jixin ZhongDivision of Cardiology, Department of Medicine, University of Maryland School of Medicine, Baltimore, MD.
Xiaoquan Rao
Zachary Braunstein
Anne Taylor
Vimal Narula
Jeffrey Hazey
Dean Mikami
Bradley Needleman
Jessica Rutsky
Qinghua Sun
Jeffrey A Deiuliis
Abhay R Satoskar
Sanjay Rajagopalan
The Ohio State University · USUniversity of Maryland, Baltimore · USLung Institute · US

Funding

Air Pollution and Hypertension: Vascular MechanismsR01ES015146 · NIEHS · UNIVERSITY OF MARYLAND BALTIMORE · PI RAJAGOPALAN, SANJAY · 2007 to 2018
$4.5M
Diet-Environment Interactions in InflammationR01ES017290 · NIEHS · UNIVERSITY OF MARYLAND BALTIMORE · PI RAJAGOPALAN, SANJAY · 2010 to 2014
$1.8M
T Regulatory Cells as Determinants of Inflammation in Adipose TissueR21DK088522 · NIDDK · OHIO STATE UNIVERSITY · PI RAJAGOPALAN, SANJAY · 2010 to 2011
$417k
Inflammatory Mechanisms In Insulin ResistanceF32DK083903 · NIDDK · OHIO STATE UNIVERSITY · PI DEIULIIS, JEFFREY ALAN · 2009 to 2011
$157k
NHLBI NIH HHS R21-HL-108467NIDDK NIH HHS F32 DK083903NIDDK NIH HHS R21 DK088522NIDDK NIH HHS R21-DK-088522NIEHS NIH HHS R01 ES015146NIEHS NIH HHS R01-ES-015146NIEHS NIH HHS R01 ES017290NIEHS NIH HHS R01-ES-017290
6 · The paper itself

Abstract

A key pathophysiologic role for activated T-cells in mediating adipose inflammation and insulin resistance (IR) has been recently postulated. However, mechanisms underlying their activation are poorly understood. In this study, we demonstrated a previously unrecognized homeostatic role for the costimulatory B7 molecules (CD80 and CD86) in preventing adipose inflammation. Instead of promoting inflammation, which was found in many other disease conditions, B7 costimulation reduced adipose inflammation by maintaining regulatory T-cell (Treg) numbers in adipose tissue. In both humans and mice, expression of CD80 and CD86 was negatively correlated with the degree of IR and adipose tissue macrophage infiltration. Decreased B7 expression in obesity appeared to directly impair Treg proliferation and function that lead to excessive proinflammatory macrophages and the development of IR. CD80/CD86 double knockout (B7 KO) mice had enhanced adipose macrophage inflammation and IR under both high-fat and normal diet conditions, accompanied by reduced Treg development and proliferation. Adoptive transfer of Tregs reversed IR and adipose inflammation in B7 KO mice. Our results suggest an essential role for B7 in maintaining Tregs and adipose homeostasis and may have important implications for therapies that target costimulation in type 2 diabetes.

Indexed as

Adipose TissueAdoptive TransferAnimalsB7-1 AntigenB7-2 AntigenCell ProliferationHomeostasisHumansInflammationInsulin ResistanceLymphocyte ActivationMacrophagesMiceMice, KnockoutT-Lymphocytes, RegulatoryB7-1 AntigenB7-2 AntigenCd86 protein, mouse

Identifiers

PMID24222350
PMCPMC4179314
OpenAlexW2160956885

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.