rdf:type |
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lifeskim:mentions |
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pubmed:issue |
10
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pubmed:dateCreated |
2009-11-25
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pubmed:abstractText |
Many models of transplant tolerance have been found to depend on the induction of regulatory T cells (Tregs). Innate immune signals are known to suppress Tregs thereby augmenting immunity by abrogating Treg function. Such signals may also provide a barrier to transplantation tolerance mediated by Tregs. A number of cell surface molecules expressed by Tregs have been found to inhibit Treg activity, the best characterized of which is the glucocorticoid-induced tumor necrosis factor receptor-related (GITR) protein.
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pubmed:grant |
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Epitopes,
http://linkedlifedata.com/resource/pubmed/chemical/Glucocorticoid-Induced...,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Nerve Growth Factor,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Tumor Necrosis Factor,
http://linkedlifedata.com/resource/pubmed/chemical/Tnfrsf18 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Tnfsf18 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factors
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
1534-6080
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pubmed:author |
pubmed-author:CatonAndrew JAJ,
pubmed-author:ChoiYongwonY,
pubmed-author:DengShaopingS,
pubmed-author:DuffPatrick EPE,
pubmed-author:KimJames IJI,
pubmed-author:LeeMajor KMK,
pubmed-author:LeeSeoung-HoonSH,
pubmed-author:LianMoh-MohMM,
pubmed-author:MarkmannJames FJF,
pubmed-author:MooreDaniel JDJ,
pubmed-author:SonawaneSamsher BSB,
pubmed-author:YehHeidiH
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pubmed:issnType |
Electronic
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pubmed:day |
27
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pubmed:volume |
88
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1169-77
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:19935370-Animals,
pubmed-meshheading:19935370-CD4-Positive T-Lymphocytes,
pubmed-meshheading:19935370-Crosses, Genetic,
pubmed-meshheading:19935370-Epitopes,
pubmed-meshheading:19935370-Flow Cytometry,
pubmed-meshheading:19935370-Glucocorticoid-Induced TNFR-Related Protein,
pubmed-meshheading:19935370-Graft Survival,
pubmed-meshheading:19935370-Humans,
pubmed-meshheading:19935370-Immunosuppression,
pubmed-meshheading:19935370-Inflammation,
pubmed-meshheading:19935370-Lymphocytes,
pubmed-meshheading:19935370-Mice,
pubmed-meshheading:19935370-Mice, Inbred BALB C,
pubmed-meshheading:19935370-Mice, Transgenic,
pubmed-meshheading:19935370-Receptors, Nerve Growth Factor,
pubmed-meshheading:19935370-Receptors, Tumor Necrosis Factor,
pubmed-meshheading:19935370-Signal Transduction,
pubmed-meshheading:19935370-Skin Transplantation,
pubmed-meshheading:19935370-Survival Rate,
pubmed-meshheading:19935370-T-Lymphocytes, Regulatory,
pubmed-meshheading:19935370-Transplantation, Homologous,
pubmed-meshheading:19935370-Tumor Necrosis Factors
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pubmed:year |
2009
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pubmed:articleTitle |
GITR Blockade Facilitates Treg Mediated Allograft Survival.
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pubmed:affiliation |
Department of Medicine, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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