Evidence map›Paper›PMID 21166993›Full record

ArticleJournal of thrombosis and haemostasis : JTH2011

Microvascular thrombosis and CD40/CD40L signaling.

F N E Gavins, G Li, J Russell, M Perretti, D N Granger

Open access · bronzeAbstract read
In one paragraph

Article in Journal of thrombosis and haemostasis : JTH, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
0.1field-weighted citation impact, top 49% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Observational
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Integrative Medicine on Optimizing Clopidogrel and Aspirin Therapy.Chinese journal of integrative medicine · 2019
    Review
  13. Article
  14. Article
  15. Biomarkers of Inflammation, Thrombogenesis, and Collagen Turnover in Patients With Atrial Fibrillation.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis · 2018
    Article
  16. CD40L and Its Receptors in Atherothrombosis-An Update.Frontiers in cardiovascular medicine · 2017
    Review
  17. Article
  18. Article
  19. Article
  20. Review
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

5 authors at 3 institutions in 2 countries.

F N E GavinsWolfson Neuroscience Laboratories, Faculty of Medicine, Imperial College, London, UK. f.gavins@imperial.ac.uk
G Li
J Russell
M Perretti
D N Granger
Louisiana State University Health Sciences Center Shreveport · USImperial College London · GBQueen Mary University of London · GB

Funding

TRANSCAPILLARY FLUID EXCHANGER01HL026441 · NHLBI · UNIVERSITY OF SOUTH ALABAMA · PI GRANGER, D. NEIL · 1985 to 2013
$4.0M
Mechanisms of CD40/CD40L in vascular injury and repairR01HL087990 · NHLBI · LOUISIANA STATE UNIV HSC SHREVEPORT · PI LI, GUOHONG · 2008 to 2013
$1.6M
Biotechnology and Biological Sciences Research Council BB/E52708X/1NHLBI NIH HHS HL087990NHLBI NIH HHS HL26441NHLBI NIH HHS R01 HL026441NHLBI NIH HHS R01 HL087990NIDDK NIH HHS P01 DK43788
6 · The paper itself

Abstract

backgroundAlthough inflammation and thrombosis are now recognized to be interdependent processes that activate and perpetuate each other, the signaling molecules that link these two processes remain poorly understood.

objectivesThe objective of this study was to assess the contribution of the CD40/CD40L signaling system to the enhanced microvascular thrombosis that accompanies two distinct experimental models of inflammation, that is, endotoxemia (lipopolysaccharide [LPS]) and dextran sodium sulfate (DSS)-induced colitis.

methodsThrombosis was induced in cerebral (LPS model) and cremaster muscle (DSS model) arterioles and venules of wild-type (WT) mice and mice deficient in either CD40 (CD40(-/-)) or CD40L (CD40L(-/-)), using the light/dye (photoactivation) method. RESULTS AND

conclusionsA comparison of thrombus formation between WT and mutant mice revealed a role for CD40 and/or CD40L in the inflammation-enhanced thrombosis responses in both of the cerebral and muscle vasculatures. However, the relative contributions of CD40 and its ligand to thrombus formation differed between vascular beds (brain vs. muscle) and vessel types (arterioles vs. venules). The protective effect of CD40L deficiency in cerebral arterioles exposed to LPS was significantly blunted by administration of soluble CD40L. These findings implicate CD40 and its ligand in the enhanced thrombus formation that is associated with acute and chronic inflammation.

Indexed as

AnimalsCD40 AntigensCD40 LigandCerebrovascular DisordersColitisDextran SulfateDisease Models, AnimalInflammationLipopolysaccharidesMaleMiceMice, Inbred C57BLMice, KnockoutMicrovesselsMuscle, SkeletalSignal TransductionCD40 AntigensCD40 LigandDextran SulfateLipopolysaccharides

Identifiers

PMID21166993
PMCPMC3050075
OpenAlexW1485099836

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.