Evidence map›Paper›PMID 19745158›Full record

ArticleJournal of leukocyte biology2010

Enhanced production of IL-17A during zymosan-induced peritonitis in obese mice.

Maria Pini, Giamila Fantuzzi

Abstract readComparative Study
In one paragraph

Article in Journal of leukocyte biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 54 citations in OpenAlex.

  1. Review
  2. Article
  3. Diet-induced obesity in mice impairs host defense againstAmerican journal of physiology. Lung cellular and molecular physiology · 2022
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Interleukin-17A Gene Expression in Morbidly Obese Women.International journal of molecular sciences · 2015
    Article
  9. Review
  10. Article
  11. Article
  12. Role of T cells in malnutrition and obesity.Frontiers in immunology · 2014
    Review
  13. Article
  14. Article
  15. Obesity and airway responsiveness: role of TNFR2.Pulmonary pharmacology & therapeutics · 2013
    Article
  16. Stress and obesity as risk factors in cardiovascular diseases: a neuroimmune perspective.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2013
    Review
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Maria PiniDepartment of Kinesiology, University of Illinois, Chicago, IL 60612, USA.
Giamila Fantuzzi
University of Illinois Chicago · US

Funding

Role of Leptin in murine modeles of IBDR01DK061483 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI FANTUZZI, GIAMILA · 2003 to 2007
$1.5M
NIDDK NIH HHS DK061483NIDDK NIH HHS R01 DK061483
6 · The paper itself

Abstract

IL-17A is a proinflammatory cytokine critical for host defense and involved in the pathogenesis of autoimmune disorders. Obesity is associated with chronic low-grade inflammation but also with a heightened acute inflammatory response. We investigated the effect of obesity on IL-17A production using the model of ZY-induced peritonitis. Compared with lean controls, administration of ZY induced a significantly exacerbated inflammatory response in obese leptin-deficient ob/ob mice and in mice with diet-induced obesity (DIO). Levels of IL-17A in the peritoneal fluid in response to ZY were elevated significantly in ob/ob and DIO mice compared with lean animals. Reconstitution of ob/ob mice with exogenous leptin did not alter production of IL-17A significantly in response to ZY. Peritoneal cells and adipose tissue obtained from ZY-injected obese mice expressed significantly higher levels of IL-17A mRNA compared with lean mice. Approximately 2% of peritoneal Ly6G(+) neutrophils from ZY-injected obese mice expressed IL-17A protein, compared with 0.2% of cells obtained from lean mice. Neutralization of IL-17 in ob/ob mice inhibited neutrophil recruitment and production of neutrophil-attracting CXC chemokines and IL-6, without affecting macrophage infiltration or levels of IL-10 and the chemokine CCL2. In contrast, neutralization of IL-6 did not affect production of IL-17A or chemokines while reducing production of the acute-phase protein serum amyloid A significantly. These data demonstrate that neutrophil-derived IL-17A is increased in obese mice during acute inflammation and contributes to exacerbation of inflammatory responses.

Indexed as

Acute DiseaseAnimalsAscitic FluidChemokines, CXCDietary FatsFemaleGene Expression RegulationInflammationInterleukin-17Interleukin-6 InhibitorsIntra-Abdominal FatLeptinMaleMiceMice, Inbred C57BLMice, ObeseChemokines, CXCDietary FatsIl17a protein, mouseInterleukin-17Interleukin-6 InhibitorsLeptinZymosan

Identifiers

PMID19745158
PMCPMC3210562
OpenAlexW2120302928

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.