Evidence map›Paper›PMID 19059114›Full record

ArticleThe Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation2008

CXCL12 induction of inducible nitric oxide synthase in human CD8 T cells.

Jonathan C Choy, Tai Yi, Deepak A Rao, George Tellides, Karen Fox-Talbot, William M Baldwin, Jordan S Pober

Open access · greenAbstract read
In one paragraph

Article in The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 27% 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

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

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Generation of NO by bystander human CD8 T cells augments allogeneic responses by inhibiting cytokine deprivation-induced cell death.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2009
    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

7 authors at 2 institutions in 1 country.

Jonathan C ChoyDepartment of Immunobiology, Yale University School of Medicine, New Haven, Connecticut 06520-8089, USA.
Tai Yi
Deepak A Rao
George Tellides
Karen Fox-Talbot
William M Baldwin
Jordan S Pober
Yale University · USJohns Hopkins University · US

Funding

SOCS-1 and endothelial dysfunction in graft arteriosclerosisP01HL070295 · NHLBI · YALE UNIVERSITY · PI SESSA, WILLIAM C · 2001 to 2010
$17.9M
Role of the Granzyme B Pathway in AGAP01HL056091 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI BALDWIN, WILLIAM M · 1997 to 2007
$10.9M
NHLBI NIH HHS HL070295NHLBI NIH HHS P01 HL056091NHLBI NIH HHS P01 HL070295NHLBI NIH HHS P01-HL56091
6 · The paper itself

Abstract

backgroundWe reported previously that inducible nitric oxide synthase (iNOS) expression in graft-infiltrating human T cells that is confined to the bystander population contributes to T- cell-mediated rejection of allograft arteries in a humanized mouse model. Herein we examine whether CXCL12, a chemokine thought to contribute to recruitment of bystander T cells, induces iNOS in human CD8 T cells.

methodsHuman CD8 T cells were treated with CXCL12 and iNOS expression was examined. Also, human allograft arteries were immunohistochemically stained for iNOS and CD8, and adjacent sections stained for CXCL12 to determine their localization in human tissues.

resultsResting human CD8 and CD4 T cells expressed the CXCR4, but not the CXCR7, receptor for CXCL12. Treatment with CXCL12 induced expression of both iNOS mRNA and protein in primary human CD8 T cells in a dose-dependent manner, but had no effect on CD4 T cells. Induction of iNOS expression in CD8 T cells was mediated by increased gene transcription. T-cell-receptor (TCR)-activated CD8 T cells rapidly downregulated CXCR4, which coincided with diminished ability of CXCL12 to induce iNOS in activated T cells. iNOS expression in infiltrating human CD8 T cells was spatially associated with CXCL12 expression both in the humanized mouse model of allograft artery rejection and in clinical specimens of coronary arteries displaying allograft vasculopathy.

conclusionsCXCL12 induces iNOS expression in human CD8 T cells and this response may contribute to allograft rejection.

Indexed as

AnimalsArteriesCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCells, CulturedChemokine CXCL12Coronary VesselsDisease Models, AnimalFlow CytometryGenes, ReporterGraft RejectionHeart TransplantationHumansMiceMice, Inbred StrainsNitric Oxide Synthase Type IIChemokine CXCL12Nitric Oxide Synthase Type IIRNA, Messenger

Identifiers

PMID19059114
PMCPMC2645593
OpenAlexW2068555922

What OpenQuestion holds

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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.