Evidence map›Paper›PMID 25972484›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2015

Cutting edge: Role of osteopontin and integrin αv in T cell-mediated anti-inflammatory responses in endotoxemia.

Makoto Inoue, Mari L Shinohara

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

14 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Definition of the contribution of an Osteopontin-producing CD11cProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  8. Article
  9. Secreted osteopontin from CD4Cell reports · 2021
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. 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

2 authors at 1 institution in 1 country.

Makoto InoueDepartment of Immunology, Duke University School of Medicine, Durham, NC 27710; and.
Mari L ShinoharaDepartment of Immunology, Duke University School of Medicine, Durham, NC 27710; and Department of Molecular Genetics and Microbiology, Duke University School of Medicine, Durham, NC 27710 mari.shinohara@duke.edu.
Duke University · US

Funding

Role of osteopontin in innate immunity during infections and inflammationR01AI088100 · NIAID · DUKE UNIVERSITY · PI SHINOHARA, MARI L. · 2011 to 2021
$4.3M
Regulation of innate inflammation by CD40 signaling and intracellular osteopontinR21AI103584 · NIAID · DUKE UNIVERSITY · PI SHINOHARA, MARI L. · 2014 to 2015
$432k
NIAID NIH HHS R01 AI088100NIAID NIH HHS R01-AI088100NIAID NIH HHS R21 AI103584NIAID NIH HHS R21-AI103584
6 · The paper itself

Abstract

The immune system is equipped with mechanisms that downregulate hyperinflammation to avoid collateral damage. We demonstrated recently that unprimed T cells downregulate macrophage TNF production through direct interaction with macrophages in the spleen during LPS endotoxemia. How T cell migration toward macrophages occurs upon LPS injection is still not clear. In this study, we demonstrate that secreted osteopontin (sOPN) plays a role in the T cell migration to initiate the suppression of hyperinflammation during endotoxemia. Osteopontin levels in splenic macrophages were upregulated 2 h after LPS treatment, whereas T cell migration toward macrophages was observed 3 h after treatment. Neutralization of sOPN and blockade of its receptor, integrin αv, significantly inhibited CD4(+) T cell migration and increased susceptibility to endotoxemia. Our study demonstrates that the sOPN/integrin αv axis, which induces T cell chemotaxis toward macrophages, is critical for suppressing hyperinflammation during the first 3 h of endotoxemia.

Indexed as

AnimalsCell MovementDisease Models, AnimalEndotoxemiaFemaleInflammationIntegrin alpha5beta1LipopolysaccharidesMacrophagesMaleMiceMice, KnockoutModels, BiologicalOsteopontinSpleenT-LymphocytesIntegrin alpha5beta1LipopolysaccharidesOsteopontin

Identifiers

PMID25972484
PMCPMC4458449
OpenAlexW1566499394

What OpenQuestion holds

Textmetadata
LicenceTDM
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.