Source:http://linkedlifedata.com/resource/pubmed/id/16339526
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
2005-12-12
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pubmed:abstractText |
Skin dendritic cells (DC) are professional APC critical for initiation and control of adaptive immunity. In the present work we have analyzed the CD4+ T cell stimulatory function of different subsets of DC that migrate spontaneously from human skin explants, including CD1a+CD14- Langerhans' cells (LC), CD1a-CD14- dermal DC (DDC), and CD1a-CD14+ LC precursors. Skin migratory DC consisted of APC at different stages of maturation-activation that produced IL-10, TGF-beta1, IL-23p19, and IL-12p40, but did not release IL-12p70 even after exposure to DC1-driving stimuli. LC and DDC migrated as mature/activated APC able to stimulate allogeneic naive CD4+ T cells and to induce memory Th1 cells in the absence of IL-12p70. The potent CD4+ T cell stimulatory function of LC and DDC correlated with their high levels of expression of MHC class II, adhesion, and costimulatory molecules. The Th1-biasing function of LC and DDC depended on their ability to produce IL-23. By contrast, CD1a-CD14+ LC precursors migrated as immature-semimature APC and were weak stimulators of allogeneic naive CD4+ T cells. However, and opposite of a potential tolerogenic role of immature DC, the T cell allostimulatory and Th1-biasing function of CD14+ LC precursors increased significantly by augmenting their cell number, prolonging the time of interaction with responding T cells, or addition of recombinant human IL-23 in MLC. The data presented in this study provide insight into the function of the complex network of skin-resident DC that migrate out of the epidermis and dermis after cutaneous immunizations, pathogen infections, or allograft transplantation.
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pubmed:grant |
http://linkedlifedata.com/resource/pubmed/grant/AI51698,
http://linkedlifedata.com/resource/pubmed/grant/R01AI06008,
http://linkedlifedata.com/resource/pubmed/grant/R01AI41011,
http://linkedlifedata.com/resource/pubmed/grant/R01CA100893,
http://linkedlifedata.com/resource/pubmed/grant/R01HL075512,
http://linkedlifedata.com/resource/pubmed/grant/R01HL077545,
http://linkedlifedata.com/resource/pubmed/grant/R21AI55027,
http://linkedlifedata.com/resource/pubmed/grant/R21AI57958,
http://linkedlifedata.com/resource/pubmed/grant/R21HL69725,
http://linkedlifedata.com/resource/pubmed/grant/U01AI056488
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD1,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD14,
http://linkedlifedata.com/resource/pubmed/chemical/CD1a antigen,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukins,
http://linkedlifedata.com/resource/pubmed/chemical/TGFB1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Transforming Growth Factor beta,
http://linkedlifedata.com/resource/pubmed/chemical/Transforming Growth Factor beta1
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
175
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
7905-15
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:16339526-Antigen-Presenting Cells,
pubmed-meshheading:16339526-Antigens, CD1,
pubmed-meshheading:16339526-Antigens, CD14,
pubmed-meshheading:16339526-CD4-Positive T-Lymphocytes,
pubmed-meshheading:16339526-Cell Movement,
pubmed-meshheading:16339526-Cells, Cultured,
pubmed-meshheading:16339526-Dendritic Cells,
pubmed-meshheading:16339526-Humans,
pubmed-meshheading:16339526-Interleukins,
pubmed-meshheading:16339526-Lymphocyte Activation,
pubmed-meshheading:16339526-Skin,
pubmed-meshheading:16339526-Th1 Cells,
pubmed-meshheading:16339526-Transforming Growth Factor beta,
pubmed-meshheading:16339526-Transforming Growth Factor beta1
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pubmed:year |
2005
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pubmed:articleTitle |
CD4+ T cell responses elicited by different subsets of human skin migratory dendritic cells.
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pubmed:affiliation |
Department of Dermatology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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