rdf:type |
|
lifeskim:mentions |
umls-concept:C0017262,
umls-concept:C0025260,
umls-concept:C0031437,
umls-concept:C0039194,
umls-concept:C0086418,
umls-concept:C0108783,
umls-concept:C0185117,
umls-concept:C0220905,
umls-concept:C0229664,
umls-concept:C1332714,
umls-concept:C1334114,
umls-concept:C1414412,
umls-concept:C2911684
|
pubmed:issue |
11
|
pubmed:dateCreated |
2010-10-27
|
pubmed:abstractText |
We have shown that CD39 and CD73 are coexpressed on the surface of murine CD4+ Foxp3+ regulatory T cells (Treg) and generate extracellular adenosine, contributing to Treg immunosuppressive activity. We now describe that CD39, independently of CD73, is expressed by a subset of blood-derived human CD4+ CD25+ CD127lo Treg, defined by robust expression of Foxp3. A further distinct population of CD4+ CD39+ T lymphocytes can be identified, which do not express CD25 and FoxP3 and exhibit the memory effector cellular phenotype. Differential expression of CD25 and CD39 on circulating CD4+ T cells distinguishes between Treg and pathogenic cellular populations that secrete proinflammatory cytokines such as IFN? and IL-17. These latter cell populations are increased, with a concomitant decrease in the CD4+ CD25+ CD39+ Tregs, in the peripheral blood of patients with renal allograft rejection. We conclude that the ectonucleotidase CD39 is a useful and dynamic lymphocytes surface marker that can be used to identify different peripheral blood T cell-populations to allow tracking of these in health and disease, as in renal allograft rejection.
|
pubmed:grant |
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD4,
http://linkedlifedata.com/resource/pubmed/chemical/Apyrase,
http://linkedlifedata.com/resource/pubmed/chemical/CD39 antigen,
http://linkedlifedata.com/resource/pubmed/chemical/IL17A protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/IL2RA protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-17,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-2 Receptor alpha Subunit,
http://linkedlifedata.com/resource/pubmed/chemical/Pyrophosphatases,
http://linkedlifedata.com/resource/pubmed/chemical/ectonucleotide pyrophosphohydrolase
|
pubmed:status |
MEDLINE
|
pubmed:month |
Nov
|
pubmed:issn |
1600-6143
|
pubmed:author |
pubmed-author:DeaglioSS,
pubmed-author:DohertyGG,
pubmed-author:DwyerK MKM,
pubmed-author:GalPP,
pubmed-author:HanidziarDD,
pubmed-author:HillP APA,
pubmed-author:KoulmandaMM,
pubmed-author:McRaeJ LJL,
pubmed-author:PommerLL,
pubmed-author:PuthetiPP,
pubmed-author:RobsonS CSC,
pubmed-author:StromT BTB,
pubmed-author:WinterhalterAA
|
pubmed:copyrightInfo |
©2010 The Authors Journal compilation©2010 The American Society of Transplantation and the American Society of Transplant Surgeons.
|
pubmed:issnType |
Electronic
|
pubmed:volume |
10
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
2410-20
|
pubmed:dateRevised |
2011-11-1
|
pubmed:meshHeading |
pubmed-meshheading:20977632-Antigens, CD,
pubmed-meshheading:20977632-Antigens, CD4,
pubmed-meshheading:20977632-Apyrase,
pubmed-meshheading:20977632-CD4-Positive T-Lymphocytes,
pubmed-meshheading:20977632-Graft Rejection,
pubmed-meshheading:20977632-Humans,
pubmed-meshheading:20977632-Immunologic Memory,
pubmed-meshheading:20977632-Interferon-gamma,
pubmed-meshheading:20977632-Interleukin-17,
pubmed-meshheading:20977632-Interleukin-2 Receptor alpha Subunit,
pubmed-meshheading:20977632-Kidney Failure, Chronic,
pubmed-meshheading:20977632-Kidney Transplantation,
pubmed-meshheading:20977632-Phenotype,
pubmed-meshheading:20977632-Pyrophosphatases,
pubmed-meshheading:20977632-T-Lymphocyte Subsets,
pubmed-meshheading:20977632-T-Lymphocytes, Regulatory,
pubmed-meshheading:20977632-Th17 Cells
|
pubmed:year |
2010
|
pubmed:articleTitle |
Expression of CD39 by human peripheral blood CD4+ CD25+ T cells denotes a regulatory memory phenotype.
|
pubmed:affiliation |
Immunology Research Centre, Department of Medicine, St. Vincent's Hospital, The University of Melbourne, Melbourne, Victoria, Australia.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
|