Evidence map›Paper›PMID 19917689›Full record

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

Role of T cell TGFbeta signaling and IL-17 in allograft acceptance and fibrosis associated with chronic rejection.

Susan M Faust, Guanyi Lu, Bernard L Marini, Weiping Zou, David Gordon, Yoichiro Iwakura, Yasmina Laouar, D Keith Bishop

Open access · bronzeAbstract 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 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

40 citing papers in PubMed, 67 citations in OpenAlex.

  1. Chronic Rejection in Facial Vascularized Composite Allotransplantation (fVCA).Results and problems in cell differentiation · 2026
    Review
  2. How Cytokines Regulate Immune Response Toward Chronic Allograft Rejection?Results and problems in cell differentiation · 2026
    Review
  3. Article
  4. The role of IL-17 family cytokines in cardiac fibrosis.Frontiers in cardiovascular medicine · 2024
    Review
  5. Immune mechanisms in fibrotic pulmonary sarcoidosis.European respiratory review : an official journal of the European Respiratory Society · 2022
    Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Measurement of T Cell Alloreactivity Using Imaging Flow Cytometry.Journal of visualized experiments : JoVE · 2017
    Article
  18. Article
  19. Article
  20. 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

8 authors at 3 institutions in 4 countries.

Susan M FaustDepartment of Surgery, University of Michigan School of Medicine, Ann Arbor, MI 48109, USA.
Guanyi Lu
Bernard L Marini
Weiping Zou
David Gordon
Yoichiro Iwakura
Yasmina Laouar
D Keith Bishop
University of Michigan · USNational Institute of Pathology · INTokyo University of Science · JP

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 main barrier to long-term transplant survival. CR is a progressive disease defined by interstitial fibrosis, vascular neointimal development, and graft dysfunction. The underlying mechanisms responsible for CR remain poorly defined. TGFbeta has been implicated in promoting fibrotic diseases including CR, but is beneficial in the transplant setting due to its immunosuppressive activity. To assess the requirement for T cell TGFbeta signaling in allograft acceptance and the progression of CR, we used mice with abrogated T cell TGFbeta signaling as allograft recipients. We compared responses from recipients that were transiently depleted of CD4(+) cells (that develop CR and express intragraft TGFbeta) with responses from mice that received anti-CD40L mAb therapy (that do not develop CR and do not express intragraft TGFbeta). Allograft acceptance and suppression of graft-reactive T and B cells were independent of T cell TGFbeta signaling in mice treated with anti-CD40L mAb. In recipients transiently depleted of CD4(+) T cells, T cell TGFbeta signaling was required for the development of fibrosis associated with CR, long-term graft acceptance, and suppression of graft-reactive T and B cell responses. Furthermore, IL-17 was identified as a critical element in TGFbeta-driven allograft fibrosis. Thus, IL-17 may provide a therapeutic target for preventing graft fibrosis, a measure of CR, while sparing the immunosuppressive activity of TGFbeta.

Indexed as

AnimalsChronic DiseaseFibrosisFlow CytometryGraft RejectionGraft SurvivalHeart TransplantationHumansImmunohistochemistryInterleukin-17MiceMice, Inbred BALB CMice, Inbred C57BLReverse Transcriptase Polymerase Chain ReactionSignal TransductionT-LymphocytesInterleukin-17Transforming Growth Factor beta

Identifiers

PMID19917689
PMCPMC2819141
OpenAlexW2150750743

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.