Evidence map›Paper›PMID 23479618›Full record

Trial reportProceedings of the National Academy of Sciences of the United States of America2013

B cells promote inflammation in obesity and type 2 diabetes through regulation of T-cell function and an inflammatory cytokine profile.

Jason DeFuria, Anna C Belkina, Madhumita Jagannathan-Bogdan, Jennifer Snyder-Cappione, Jordan David Carr, Yanina R Nersesova, Douglas Markham, Katherine J Strissel, Amanda A Watkins, Min Zhu and 9 more

Registry-linked trialAbstract readClinical Trial
In one paragraph

Trial report in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05591339 (Diabetes Diagnosis, Management, Prevention and Education in Guinea-Bissau), which is not on this map. Cited by 309 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
309citing papers in PubMed, 5 pooled it
–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.

NCT05591339 phase4active not recruitingnot on this mapstarted 2023, after this paper: background citation

Diabetes Diagnosis, Management, Prevention and Education in Guinea-Bissau

TypeinterventionalSponsorBandim Health ProjectRan2023 to 2029Enrolled200ConditionsDiabetes Mellitus, BCG Vaccination ReactionArmsBCG vaccine (two doses, 4 weeks apart), Saline placebo (Two doses, 4 weeks apart)
3 · Its place in the literature

Who cites it

309 citing papers in PubMed, 5 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Type 2 Diabetes: How Much of an Autoimmune Disease?Frontiers in endocrinology · 2019
    Pooled it
  6. Trial
  7. Trial
  8. Review
  9. Review
  10. Article
  11. Article
  12. Observational
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Diabesity and Oral Immunity: Exploring the Interconnection.Advances in experimental medicine and biology · 2026
    Review
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors.

Jason DeFuriaDepartment of Microbiology, Boston University School of Medicine, Boston, MA 02118, USA.
Anna C Belkina
Madhumita Jagannathan-Bogdan
Jennifer Snyder-Cappione
Jordan David Carr
Yanina R Nersesova
Douglas Markham
Katherine J Strissel
Amanda A Watkins
Min Zhu
Jessica Allen
Jacqueline Bouchard
Gianluca Toraldo
Ravi Jasuja
Martin S Obin
Marie E McDonnell
Caroline Apovian
Gerald V Denis
Barbara S Nikolajczyk

Funding

Transgenic CoreP30DK046200 · NIDDK · TUFTS MEDICAL CENTER · PI GREENBERG, ANDREW S, PERISSI, VALENTINA · 1992 to 2021
$25.0M
RESEARCH TRAINING IN IMMUNOLOGYT32AI007309 · NIAID · BOSTON UNIVERSITY MEDICAL CAMPUS · PI GUMMULURU, SURYARAM · 1988 to 2024
$7.4M
RESEARCH TRAINING IN BLOOD DISEASES AND RESOURCEST32HL007501 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI LERNER, ADAM, STEINBERG, MARTIN H. · 1985 to 2018
$5.4M
Uncoupling obesity from breast cancer in African American womenU01CA182898 · NCI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI DENIS, GERALD V, PALMER, JULIE R · 2013 to 2017
$3.1M
The Role of B Cells and B Cell Toll-like Receptors in Periodontal DiseaseR21DE021154 · NIDCR · BOSTON UNIVERSITY MEDICAL CAMPUS · PI NIKOLAJCZYK, BARBARA · 2011 to 2012
$449k
The Role of B Cells and B Cell Toll-like Receptors in Glucose IntoleranceR21DK089270 · NIDDK · BOSTON UNIVERSITY MEDICAL CAMPUS · PI NIKOLAJCZYK, BARBARA · 2010 to 2011
$446k
The Role of Lymphocytes in Diet-Induced Metabolic DiseaseR56DK096525 · NIDDK · BOSTON UNIVERSITY MEDICAL CAMPUS · PI NIKOLAJCZYK, BARBARA · 2012 to 2012
$193k
Mechanisms of Brd2 immunoprotection from insulin resistanceR56DK090455 · NIDDK · BOSTON UNIVERSITY MEDICAL CAMPUS · PI DENIS, GERALD V · 2011 to 2011
$54k
NCI NIH HHS U01 CA182898NHLBI NIH HHS HL007501NHLBI NIH HHS T32 HL007501NIAID NIH HHS AI007309NIAID NIH HHS T32 AI007309NIDCR NIH HHS 5R21DE021154NIDCR NIH HHS R21 DE021154NIDDK NIH HHS DK046200NIDDK NIH HHS P30 DK046200NIDDK NIH HHS R21 DK089270NIDDK NIH HHS R21DK089270NIDDK NIH HHS R56 DK090455NIDDK NIH HHS R56 DK096525
6 · The paper itself

Abstract

Patients with type 2 diabetes (T2D) have disease-associated changes in B-cell function, but the role these changes play in disease pathogenesis is not well established. Data herein show B cells from obese mice produce a proinflammatory cytokine profile compared with B cells from lean mice. Complementary in vivo studies show that obese B cell-null mice have decreased systemic inflammation, inflammatory B- and T-cell cytokines, adipose tissue inflammation, and insulin resistance (IR) compared with obese WT mice. Reduced inflammation in obese/insulin resistant B cell-null mice associates with an increased percentage of anti-inflammatory regulatory T cells (Tregs). This increase contrasts with the sharply decreased percentage of Tregs in obese compared with lean WT mice and suggests that B cells may be critical regulators of T-cell functions previously shown to play important roles in IR. We demonstrate that B cells from T2D (but not non-T2D) subjects support proinflammatory T-cell function in obesity/T2D through contact-dependent mechanisms. In contrast, human monocytes increase proinflammatory T-cell cytokines in both T2D and non-T2D analyses. These data support the conclusion that B cells are critical regulators of inflammation in T2D due to their direct ability to promote proinflammatory T-cell function and secrete a proinflammatory cytokine profile. Thus, B cells are potential therapeutic targets for T2D.

Indexed as

AnimalsB-LymphocytesCytokinesDiabetes Mellitus, Type 2FemaleHumansInflammationMaleMiceMice, ObeseObesityT-Lymphocytes, RegulatoryCytokines

Identifiers

PMID23479618
PMCPMC3612635

What OpenQuestion holds

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Registered trials

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.