Evidence map›Paper›PMID 19917705›Full record

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

TGFbeta neutralization within cardiac allografts by decorin gene transfer attenuates chronic rejection.

Susan M Faust, Guanyi Lu, Sherri C Wood, D Keith Bishop

Open access · greenAbstract 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 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

13 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Asporin, an extracellular matrix protein, is a beneficial regulator of cardiac remodeling.Matrix biology : journal of the International Society for Matrix Biology · 2022
    Article
  6. Article
  7. Article
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  12. Target-seeking antifibrotic compound enhances wound healing and suppresses scar formation in mice.Proceedings of the National Academy of Sciences of the United States of America · 2010
    Article
  13. 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

4 authors at 1 institution in 1 country.

Susan M FaustDepartment of Surgery, University of Michigan School of Medicine, Ann Arbor, MI 48109, USA.
Guanyi Lu
Sherri C Wood
D Keith Bishop
University of Michigan · US

Funding

Therapeutic Targets for Chronic Allograft RejectionR01HL070613 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BISHOP, D. KEITH · 2002 to 2014
$4.4M
Regenerative Sciences Training Program(RMI)T90DK070071 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GOLDSTEIN, STEVEN A · 2004 to 2008
$2.7M
Roles of CD40 and CD40 Ligand in Allograft RejectionR01AI061469 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BISHOP, D. KEITH · 2004 to 2008
$1.6M
NHLBI NIH HHS R01 HL070613NIAID NIH HHS R01 AI061469NIDDK NIH HHS T90 DK070071
6 · The paper itself

Abstract

Chronic allograft rejection (CR) is the leading cause of late graft failure following organ transplantation. CR is a progressive disease, characterized by deteriorating graft function, interstitial fibrosis, cardiac hypertrophy, and occlusive neointima development. TGFbeta, known for its immunosuppressive qualities, plays a beneficial role in the transplant setting by maintaining alloreactive T cells in a hyporesponsive state, but has also been implicated in promoting graft fibrosis and CR. In the mouse vascularized cardiac allograft model, transient depletion of CD4(+) cells promotes graft survival but leads to CR, which is associated with intragraft TGFbeta expression. Decorin, an extracellular matrix protein, inhibits both TGFbeta bioactivity and gene expression. In this study, gene transfer of decorin into cardiac allografts was used to assess the impact of intragraft TGFbeta neutralization on CR, systemic donor-reactive T cell responses, and allograft acceptance. Decorin gene transfer and neutralization of TGFbeta in cardiac allografts significantly attenuated interstitial fibrosis, cardiac hypertrophy, and improved graft function, but did not result in systemic donor-reactive T cell responses. Thus, donor-reactive T and B cells remained in a hyporesponsive state. These findings indicate that neutralizing intragraft TGFbeta inhibits the cytokine's fibrotic activities, but does not reverse its beneficial systemic immunosuppressive qualities.

Indexed as

AnimalsB-LymphocytesChronic DiseaseDecorinExtracellular Matrix ProteinsFibrosisGraft RejectionGraft SurvivalHeart TransplantationMiceMice, Inbred BALB CMice, Inbred C57BLProteoglycansReverse Transcriptase Polymerase Chain ReactionT-LymphocytesTransduction, GeneticDcn protein, mouseDecorinExtracellular Matrix ProteinsProteoglycansTransforming Growth Factor beta

Identifiers

PMID19917705
PMCPMC3046403
OpenAlexW2122531043

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.