Evidence map›Paper›PMID 20962257›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2010

Platelets contribute to allograft rejection through glutamate receptor signaling.

AnneMarie F Swaim, David J Field, Karen Fox-Talbot, William M Baldwin, Craig N Morrell

Open access · greenAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Glutamate Receptor Interacting Protein 1 Regulates CD4(+) CTLA-4 Expression and Transplant Rejection.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2016
    Article
  9. Article
  10. Review
  11. Platelets in early antibody-mediated rejection of renal transplants.Journal of the American Society of Nephrology : JASN · 2015
    Article
  12. Review
  13. Article
  14. Innate immune cells in transplantation.Current opinion in organ transplantation · 2014
    Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Platelets present antigen in the context of MHC class I.Journal of immunology (Baltimore, Md. : 1950) · 2012
    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

5 authors at 4 institutions in 1 country.

AnneMarie F SwaimDepartment of Molecular and Comparative Pathobiology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
David J Field
Karen Fox-Talbot
William M Baldwin
Craig N Morrell
University of Rochester · USCleveland Clinic · USJohns Hopkins Medicine · USUniversity of Baltimore · US

Funding

Surgery CoreP01AI087586 · NIAID · CLEVELAND CLINIC LERNER COM-CWRU · PI VALUJSKIKH, ANNA · 2010 to 2019
$17.2M
The Role of Platelets in Alloantibody Mediated Transplant RejectionR01HL093179 · NHLBI · UNIVERSITY OF ROCHESTER · PI MORRELL, CRAIG N · 2008 to 2012
$2.2M
Glutamate Mediates Platelet Activation through an Ionotropic Glutamate ReceptorR01HL094547 · NHLBI · UNIVERSITY OF ROCHESTER · PI MORRELL, CRAIG N · 2009 to 2012
$1.6M
NHLBI NIH HHS R01 HL093179NHLBI NIH HHS R01HL093179NHLBI NIH HHS R01HL093179-02S109NHLBI NIH HHS R01 HL094547NHLBI NIH HHS R01HL094547NIAID NIH HHS P01 AI087586NIAID NIH HHS P01AI087586-01
6 · The paper itself

Abstract

Platelets recruit leukocytes and mediate interactions between leukocytes and endothelial cells. Platelets have been long described as markers of transplant rejection, but the contribution of platelets to transplant rejection has not been critically examined. We demonstrate in this study that following T cell initiation of allograft rejection, platelets contribute to T cell recruitment and increased plasma inflammatory mediators and accelerate T cell-meditated skin graft rejection. Prior work from our laboratory has shown that platelets secrete glutamate when activated, which then induces platelet thromboxane production by signaling through platelet-expressed ionotropic glutamate receptors. Glutamate receptor antagonists therefore represent, to our knowledge, novel inhibitors of platelet-accelerated inflammation. We have found that plasma glutamate is increased in mice that receive skin grafts and that mice treated with glutamate receptor antagonists have improved graft survival and decreased plasma thromboxane, platelet factor 4 (CXCL4), and IFN-γ. Taken together, our work now demonstrates that subsequent to T cell initiation of skin graft rejection, platelets contribute to further T cell recruitment and that by blunting glutamate-mediated platelet activation, graft survival is improved.

Indexed as

AnimalsBlood PlateletsCell MovementGraft RejectionGraft SurvivalInterferon-gammaMaleMiceMice, Inbred AMice, Inbred C57BLMice, NudePlatelet ActivationReceptors, GlutamateSkin TransplantationThromboxanesT-LymphocytesInterferon-gammaReceptors, GlutamateThromboxanes

Identifiers

PMID20962257
PMCPMC3137241
OpenAlexW2128935511

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.