Evidence map›Paper›PMID 19917702›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2009

The oxazolidinone derivative locostatin induces cytokine appeasement.

Antoine Ménoret, Jeremy P McAleer, Soo-Mun Ngoi, Swagatam Ray, Nicholas A Eddy, Gabriel Fenteany, Seung-Joo Lee, Robert J Rossi, Bijay Mukherji, David L Allen and 2 more

Abstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–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.

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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Therapeutic targeting of the inflammome.Biochemical pharmacology · 2014
    Review
  8. Article
  9. Article
  10. 3-[2-(3-Methyl-quinoxalin-2-yl-oxy)eth-yl]-1,3-oxazolidin-2-one.Acta crystallographica. Section E, Structure reports online · 2010
    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

12 authors.

Antoine MénoretDepartment of Immunology, University of Connecticut Health Center, Farmington, CT 06032, USA.
Jeremy P McAleer
Soo-Mun Ngoi
Swagatam Ray
Nicholas A Eddy
Gabriel Fenteany
Seung-Joo Lee
Robert J Rossi
Bijay Mukherji
David L Allen
Nitya G Chakraborty
Anthony T Vella

Funding

PROINFLAMMATORY CYTOKINES BLOCK T CELL DEATH IN VIVOR01AI042858 · NIAID · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI VELLA, ANTHONY T · 1999 to 2016
$4.9M
Mechanism of Action of New Inhibitors of Cell MigrationR01GM077622 · NIGMS · UNIVERSITY OF CONNECTICUT STORRS · PI FENTEANY, GABRIEL · 2006 to 2010
$1.6M
Understanding the Mechanism of 4-1BB ConstimulatiuonR01AI052108 · NIAID · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI VELLA, ANTHONY T · 2003 to 2007
$1.4M
Understanding the mechanism of 4-1BB costimulationR21AI052108 · NIAID · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI VELLA, ANTHONY T. · 2002 to 2002
$326k
NIAID NIH HHS AI 42858NIAID NIH HHS AI 52108NIAID NIH HHS R01 AI042858NIAID NIH HHS R01 AI052108NIAID NIH HHS R21 AI052108NIGMS NIH HHS GM077622NIGMS NIH HHS R01 GM077622
6 · The paper itself

Abstract

Damaging inflammation arising from autoimmune pathology and septic responses results in severe cases of disease. In both instances, anti-inflammatory compounds are used to limit the excessive or deregulated cytokine responses. We used a model of robust T cell stimulation to identify new proteins involved in triggering a cytokine storm. A comparative proteomic mining approach revealed the differential mapping of Raf kinase inhibitory protein after T cell recall in vivo. Treatment with locostatin, an Raf kinase inhibitory protein inhibitor, induced T cell anergy by blocking cytokine production after Ag recall. This was associated with a reduction in Erk phosphorylation. Importantly, in vivo treatment with locostatin profoundly inhibited TNF-alpha production upon triggering the Ag-specific T cells. This effect was not limited to a murine model because locostatin efficiently inhibited cytokine secretion by human lymphocytes. Therefore, locostatin should be a useful therapeutic to control inflammation, sepsis, and autoimmune diseases.

Indexed as

AnimalsAnti-Inflammatory AgentsBlotting, WesternChromatography, LiquidClonal AnergyCytokinesElectrophoresis, Polyacrylamide GelExtracellular Signal-Regulated MAP KinasesFlow CytometryFluorescent Antibody TechniqueHumansLymphocyte ActivationMiceMice, Inbred C57BLMice, TransgenicOxazolidinonesAnti-Inflammatory AgentsCytokinesExtracellular Signal-Regulated MAP KinaseslocostatinOxazolidinonesPhosphatidylethanolamine Binding ProteinTumor Necrosis Factor-alpha

Identifiers

PMID19917702
PMCPMC2799496

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.