Evidence map›Paper›PMID 15878989›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2005

Interleukin 10 attenuates neointimal proliferation and inflammation in aortic allografts by a heme oxygenase-dependent pathway.

Sifeng Chen, Matthias H Kapturczak, Clive Wasserfall, Olena Y Glushakova, Martha Campbell-Thompson, Jessy S Deshane, Reny Joseph, Pedro E Cruz, William W Hauswirth, Kirsten M Madsen and 6 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

49 citing papers in PubMed, 108 citations in OpenAlex.

  1. Trial
  2. How Cytokines Regulate Immune Response Toward Chronic Allograft Rejection?Results and problems in cell differentiation · 2026
    Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Genetic Delivery and Gene Therapy in Pulmonary Hypertension.International journal of molecular sciences · 2021
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. HO-1 overexpression and underexpression: Clinical implications.Archives of biochemistry and biophysics · 2019
    Review
  14. Multi-Faceted Notch in Allergic Airway Inflammation.International journal of molecular sciences · 2019
    Review
  15. Article
  16. Article
  17. Heme Oxygenase 1 as a Therapeutic Target in Acute Kidney Injury.American journal of kidney diseases : the official journal of the National Kidney Foundation · 2017
    Review
  18. Article
  19. Review
  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

16 authors at 3 institutions in 1 country.

Sifeng ChenDepartment of Medicine, Nephrology Research and Training Center, University of Alabama at Birmingham, Birmingham, AL 35294.
Matthias H Kapturczak
Clive Wasserfall
Olena Y Glushakova
Martha Campbell-Thompson
Jessy S Deshane
Reny Joseph
Pedro E Cruz
William W Hauswirth
Kirsten M Madsen
Byron P Croker
Kenneth I Berns
Mark A Atkinson
Terence R Flotte
C Craig Tisher
Anupam Agarwal
University of Florida · USNorth Florida/South Georgia Veterans Health System · USUniversity of Alabama at Birmingham · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interleukin 10 (IL-10) is a pleiotropic cytokine with well known antiinflammatory, immunosuppressive, and immunostimulatory properties. Chronic allograft rejection, characterized by vascular neointimal proliferation, is a major cause of organ transplant loss, particularly in heart and kidney transplant recipients. In a Dark Agouti to Lewis rat model of aortic transplantation, we evaluated the effects of a single intramuscular injection of a recombinant adeno-associated viral vector (serotype 1) encoding IL-10 (rAAV1-IL-10) on neointimal proliferation and inflammation. rAAV1-IL-10 treatment resulted in a significant reduction of neointimal proliferation and graft infiltration with macrophages and T and B lymphocytes. The mechanism underlying the protective effects of IL-10 in aortic allografts involved heme oxygenase 1 (HO-1) because inhibition of HO activity reversed not only neointimal proliferation but also inflammatory cell infiltration. Our results indicate that IL-10 attenuates neointimal proliferation and inflammatory infiltration and strongly imply that HO-1 is an important intermediary through which IL-10 regulates the inflammatory responses associated with chronic vascular rejection.

Indexed as

Cell ProliferationAnalysis of VarianceAnimalsAortaBlotting, WesternDependovirusEndothelial CellsEnzyme-Linked Immunosorbent AssayGenetic VectorsGraft RejectionHeat-Shock ProteinsHeme Oxygenase (Decyclizing)InflammationInterleukin-10OxygenasesRatsHeat-Shock ProteinsHeme Oxygenase (Decyclizing)Hmox1 protein, ratInterleukin-10Oxygenases

Identifiers

PMID15878989
PMCPMC1090475
OpenAlexW2094993464

What OpenQuestion holds

Textmetadata
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.