Evidence map›Paper›PMID 20473306›Full record

ArticleNature medicine2010

In vivo prevention of transplant arteriosclerosis by ex vivo-expanded human regulatory T cells.

Satish N Nadig, Joanna Wieckiewicz, Douglas C Wu, Gregor Warnecke, Wei Zhang, Shiqiao Luo, Alexandru Schiopu, David P Taggart, Kathryn J Wood

Open access · greenAbstract readComparative Study
In one paragraph

Article in Nature medicine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 144 papers.

0numbers the graph read from it
0cells of the map it votes in
144citing papers in PubMed
12.8field-weighted citation impact, top 1% 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

144 citing papers in PubMed, 288 citations in OpenAlex.

  1. Article
  2. CD25Frontiers in immunology · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. The 2025 Nobel Prize in Physiology or Medicine Honors the Immune Peacekeepers.Transplant international : official journal of the European Society for Organ Transplantation · 2025
    Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Ex vivo-expanded human CD19Nature communications · 2022
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. Review

84 more citing papers are in PubMed but not listed here.

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

9 authors at 2 institutions in 1 country.

Satish N NadigTransplantation Research Immunology Group, Nuffield Department of Surgery, John Radcliffe Hospital, University of Oxford, Oxford, UK.
Joanna Wieckiewicz
Douglas C Wu
Gregor Warnecke
Wei Zhang
Shiqiao Luo
Alexandru Schiopu
David P Taggart
Kathryn J Wood
John Radcliffe Hospital · GBUniversity of Oxford · GB

Funding

Medical Research Council G0800842Wellcome Trust 082519
6 · The paper itself

Abstract

Transplant arteriosclerosis is the hallmark of chronic allograft dysfunction (CAD) affecting transplanted organs in the long term. These fibroproliferative lesions lead to neointimal thickening of arteries in all transplanted allografts. Luminal narrowing then leads to graft ischemia and organ demise. To date, there are no known tolerance induction strategies that prevent transplant arteriosclerosis. Therefore, we designed this study to test the hypothesis that human regulatory T cells (T(reg) cells) expanded ex vivo can prevent transplant arteriosclerosis. Here we show the comparative capacity of T(reg) cells, sorted via two separate strategies, to prevent transplant arteriosclerosis in a clinically relevant chimeric humanized mouse system. We found that the in vivo development of transplant arteriosclerosis in human arteries was prevented by treatment of ex vivo-expanded human T(reg) cells. Additionally, we show that T(reg) cells sorted on the basis of low expression of CD127 provide a more potent therapy to conventional T(reg) cells. Our results demonstrate that human T(reg) cells can inhibit transplant arteriosclerosis by impairing effector function and graft infiltration. We anticipate our findings to serve as a foundation for the clinical development of therapeutics targeting transplant arteriosclerosis in both allograft transplantation and other immune-mediated causes of vasculopathy.

Indexed as

AnimalsAorta, AbdominalArteriosclerosisCD4-Positive T-LymphocytesCell SeparationGraft RejectionInterferon-gammaInterleukin-2 Receptor alpha SubunitInterleukin-7 Receptor alpha SubunitLeukocytes, MononuclearMammary ArteriesMiceMice, Inbred BALB CT-Lymphocytes, RegulatoryInterferon-gammaInterleukin-2 Receptor alpha SubunitInterleukin-7 Receptor alpha Subunit

Identifiers

PMID20473306
PMCPMC2929438
OpenAlexW2027488189

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.