Source:http://linkedlifedata.com/resource/pubmed/id/19144988
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
2009-2-27
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pubmed:abstractText |
Dendritic cells (DCs) can be classified into 2 distinct subsets: conventional DCs (cDCs) and plasmacytoid DCs (pDCs). cDCs can prime antigen-specific T-cell immunity, whereas in vivo function of pDCs as antigen-presenting cells remains controversial. We evaluated the contribution of pDCs to allogeneic T-cell responses in vivo in mouse models of graft-versus-host disease (GVHD) after allogeneic hematopoietic stem cell transplantation by an add-back study of MHC-expressing pDCs into major histocompatibility complex-deficient mice that were resistant to GVHD. Alloantigen expression on pDCs alone was sufficient to prime alloreactive T cells and cause GVHD. An inflammatory environment created by host irradiation has the decisive role in maturing pDCs for T-cell priming but this process does not require Toll-like receptor signaling. Thus, functional outcomes of pDC-T-cell interactions depend on the immunologic context of encounter. To our knowledge, these results are the first to directly demonstrate an in vivo pathogenic role of pDCs as antigen-presenting cells in an antigen-specific T cell-mediated disease in the absence of other DC subsets and to provide important insight into developing strategies for tolerance induction in transplantation.
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pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1528-0020
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pubmed:author |
pubmed-author:AkashiKoichiK,
pubmed-author:AoyamaKazutoshiK,
pubmed-author:HaradaMineM,
pubmed-author:HashimotoDaigoD,
pubmed-author:KarubeKennosukeK,
pubmed-author:KoyamaMotokoM,
pubmed-author:MatsuokaKen-ichiK,
pubmed-author:NiiroHiroakiH,
pubmed-author:TanimotoMitsuneM,
pubmed-author:TeshimaTakanoriT
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pubmed:issnType |
Electronic
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pubmed:day |
26
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pubmed:volume |
113
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2088-95
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pubmed:dateRevised |
2009-6-5
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pubmed:meshHeading |
pubmed-meshheading:19144988-Animals,
pubmed-meshheading:19144988-Antigen Presentation,
pubmed-meshheading:19144988-Antigen-Presenting Cells,
pubmed-meshheading:19144988-Autoimmunity,
pubmed-meshheading:19144988-CD4-Positive T-Lymphocytes,
pubmed-meshheading:19144988-CD8-Positive T-Lymphocytes,
pubmed-meshheading:19144988-Dendritic Cells,
pubmed-meshheading:19144988-Female,
pubmed-meshheading:19144988-Genes, MHC Class II,
pubmed-meshheading:19144988-Graft vs Host Disease,
pubmed-meshheading:19144988-Lymphocyte Activation,
pubmed-meshheading:19144988-Mice,
pubmed-meshheading:19144988-Mice, Inbred BALB C,
pubmed-meshheading:19144988-Mice, Inbred C3H,
pubmed-meshheading:19144988-Mice, Inbred C57BL,
pubmed-meshheading:19144988-Mice, Knockout,
pubmed-meshheading:19144988-T-Lymphocytes
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pubmed:year |
2009
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pubmed:articleTitle |
Plasmacytoid dendritic cells prime alloreactive T cells to mediate graft-versus-host disease as antigen-presenting cells.
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pubmed:affiliation |
Department of Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Science, Fukuoka, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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