Evidence map›Paper›PMID 23225892›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2013

Adenosine A₂A receptor agonist-mediated increase in donor-derived regulatory T cells suppresses development of graft-versus-host disease.

Kyu Lee Han, Stephenie V M Thomas, Sherry M Koontz, Cattlena M Changpriroa, Seung-Kwon Ha, Harry L Malech, Elizabeth M Kang

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

21 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
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  11. [Rapamycin affect the apoptosis of splenic CD4Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2018
    Article
  12. Article
  13. Purinergic regulation of the immune system.Nature reviews. Immunology · 2016
    Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. Graft versus host disease: New insights into A2A receptor agonist therapy.Computational and structural biotechnology journal · 2015
    Review
  19. Purinergic signalling and immune cells.Purinergic signalling · 2014
    Review
  20. 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

7 authors at 3 institutions in 2 countries.

Kyu Lee HanLaboratory of Host Defenses, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Stephenie V M Thomas
Sherry M Koontz
Cattlena M Changpriroa
Seung-Kwon Ha
Harry L Malech
Elizabeth M Kang
National Institute of Allergy and Infectious Diseases · USNational Institutes of Health · USYD Global Life Science (South Korea) · KR

Funding

Development and conduct of allogeneic stem cell transplant and autologous stem cell gene therapy for inherited immune deficienciesZIAAI000989 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI KANG, ELIZABETH · 2009 to 2025
$12.4M
Basic Research on Hematopoietic Human Stem CellsZIAAI000988 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI MALECH, HARRY L · 2009 to 2019
$6.5M
Intramural NIH HHS ZIA AI000989
6 · The paper itself

Abstract

Graft-versus-host disease (GVHD) remains a significant complication of allogeneic transplantation. We previously reported that the adenosine A(2A) receptor (A(2A)R) specific agonist, ATL146e, decreases the incidence and severity of GVHD in a mouse transplant model. There is increasing interest in treatments that increase CD4(+)CD25(high)Foxp3(+) regulatory T cells (Tregs) to suppress GVHD. Our current study found in vitro that A(2A)R selective agonists enhanced TGF-β-induced generation of mouse Tregs 2.3- to 3-fold. We demonstrated in vivo suppression of GVHD with specific A(2A)R agonists in two different murine GVHD transplant models associated with profound increases in both circulating and target tissue Tregs of donor origin. Three different A(2A)R agonists of differing potency, ATL146e, ATL370, and ATL1223, all significantly inhibited GVHD-associated weight loss and mortality. At the same time, Tregs shown to be of donor origin increased 5.1- to 7.4-fold in spleen, 2.7- to 4.6-fold in peripheral blood, 2.3- to 4.7-fold in colon, and 3.8- to 4.6-fold in skin. We conclude that specific activation of A(2A)R inhibits acute GVHD through an increase of donor-derived Tregs. Furthermore, the increased presence of Tregs in target tissues (colon and skin) of A(2A)R-specific agonist-treated mice is likely the mechanistic basis for the anti-inflammatory effect preventing acute GVHD.

Indexed as

Adenosine A2 Receptor AgonistsAnimalsCell DifferentiationCells, CulturedCyclohexanecarboxylic AcidsDown-RegulationFemaleGraft vs Host DiseaseImmune ToleranceMaleMiceMice, Inbred BALB CMice, Inbred C57BLMice, Inbred DBAMice, KnockoutPurinesAdenosine A2 Receptor AgonistsATL 146eCyclohexanecarboxylic AcidsPurinesTransforming Growth Factor beta

Identifiers

PMID23225892
PMCPMC3674549
OpenAlexW2140778936

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.