Source:http://linkedlifedata.com/resource/pubmed/id/16784487
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2006-6-20
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pubmed:abstractText |
Human and mouse CD4(+)CD25(+) T cells have been intensively studied through the last decade. However, little is known about this subset in other species. This study describes the phenotype of rat CD4(+)CD25(+) Foxp3(+) T cells and the site in which they exert regulation in a transfer-induced autoimmune diabetes model. Several proteins and mRNAs are up-regulated in unstimulated rat CD4(+)CD25(+) T cells compared with CD4(+)CD25(-) T cells, including Foxp3, Lag-3, CD80, interleukin 10 (IL-10) and CTLA-4. To investigate CD4(+)CD25(+) T cells in vivo, we transferred three million diabetogenic T cells either alone or in combination with two million CD4(+)CD25(+) T cells to 30-day-old BB rats. The pancreas and the pancreatic lymph nodes were examined as two potential regulatory sites. Time-course analysis of pancreatic histology following diabetogenic T-cell transfers revealed insulitis from about 14 days after transfer. By contrast, rats receiving both diabetogenic T cells and CD4(+)CD25(+) T cells had no insulitis at any time. Moreover, the frequency of diabetogenic T cells in the pancreatic lymph nodes 2 days after transfer was significantly reduced in rats receiving both subsets. These data indicate that the primary site of T-cell regulation is in the draining lymph nodes and not the pancreas in our model.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0300-9475
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
64
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
17-29
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pubmed:dateRevised |
2008-10-10
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pubmed:meshHeading |
pubmed-meshheading:16784487-Adoptive Transfer,
pubmed-meshheading:16784487-Animals,
pubmed-meshheading:16784487-Cell Separation,
pubmed-meshheading:16784487-Diabetes Mellitus, Type 1,
pubmed-meshheading:16784487-Down-Regulation,
pubmed-meshheading:16784487-Forkhead Transcription Factors,
pubmed-meshheading:16784487-Inflammation,
pubmed-meshheading:16784487-Islets of Langerhans,
pubmed-meshheading:16784487-Lymph Nodes,
pubmed-meshheading:16784487-Pancreas,
pubmed-meshheading:16784487-Rats,
pubmed-meshheading:16784487-Rats, Inbred BB,
pubmed-meshheading:16784487-Receptors, Interleukin-2,
pubmed-meshheading:16784487-T-Lymphocyte Subsets,
pubmed-meshheading:16784487-T-Lymphocytes, Regulatory
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pubmed:year |
2006
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pubmed:articleTitle |
Characteristics of rat CD4(+)CD25(+) T cells and their ability to prevent not only diabetes but also insulitis in an adoptive transfer model in BB rats.
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pubmed:affiliation |
Hagedorn Research Institute, Gentofte, Denmark.
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pubmed:publicationType |
Journal Article
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