rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
10
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pubmed:dateCreated |
2002-5-21
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pubmed:abstractText |
Various immune diseases are considered to be regulated by the balance of T helper (Th)1 and Th2 subsets. Although Th lymphocytes are believed to be generated in draining lymph nodes (LNs), in vivo Th cell behaviors during Th1/Th2 polarization are largely unexplored. Using a murine granulomatous liver disease model induced by Propionibacterium acnes, we show that retention of Th1 cells in the LNs is controlled by a chemokine, CXCL10/interferon (IFN) inducible protein 10 produced by mature dendritic cells (DCs). Hepatic LN DCs preferentially produced CXCL10 to attract 5'-bromo-2'-deoxyuridine (BrdU)+CD4+ T cells and form clusters with IFN-gamma-producing CD4+ T cells by day 7 after antigen challenge. Blockade of CXCL10 dramatically altered the distribution of cluster-forming BrdU+CD4+ T cells. BrdU+CD4+ T cells in the hepatic LNs were selectively diminished while those in the circulation were significantly increased by treatment with anti-CXCL10 monoclonal antibody. This was accompanied by accelerated infiltration of memory T cells into the periphery of hepatic granuloma sites, most of them were in cell cycle and further produced higher amount of IFN-gamma leading to exacerbation of liver injury. Thus, mature DC-derived CXCL10 is pivotal to retain Th1 lymphocytes within T cell areas of draining LNs and optimize the Th1-mediated immune responses.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-10221917,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-10359116,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-10408488,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-10419874,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-10520991,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-10591648,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-10617422,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-10805209,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-10843381,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-10880246,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-10946253,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-10998315,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-11017102,
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http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-11034600,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-11085753,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-11104797,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-11136819,
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http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-11160258,
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http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-11673480,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-11782014,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-1640172,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-7879916,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-8600538,
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http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-9182685,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-9521319,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-9651253,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-9790904,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12021306-9835618
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Ccl21c protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Ccl22 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Chemokine CCL21,
http://linkedlifedata.com/resource/pubmed/chemical/Chemokine CCL22,
http://linkedlifedata.com/resource/pubmed/chemical/Chemokine CXCL10,
http://linkedlifedata.com/resource/pubmed/chemical/Chemokines,
http://linkedlifedata.com/resource/pubmed/chemical/Chemokines, CC,
http://linkedlifedata.com/resource/pubmed/chemical/Chemokines, CXC,
http://linkedlifedata.com/resource/pubmed/chemical/Cxcr3 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-4,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, CXCR3,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Chemokine
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0022-1007
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pubmed:author |
|
pubmed:issnType |
Print
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pubmed:day |
20
|
pubmed:volume |
195
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1257-66
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:12021306-Animals,
pubmed-meshheading:12021306-Mice,
pubmed-meshheading:12021306-Lymph Nodes,
pubmed-meshheading:12021306-Liver,
pubmed-meshheading:12021306-Propionibacterium acnes,
pubmed-meshheading:12021306-T-Lymphocytes, Helper-Inducer,
pubmed-meshheading:12021306-Granulomatous Disease, Chronic,
pubmed-meshheading:12021306-Chemotaxis, Leukocyte,
pubmed-meshheading:12021306-Interferon-gamma,
pubmed-meshheading:12021306-Interleukin-4,
pubmed-meshheading:12021306-Dendritic Cells,
pubmed-meshheading:12021306-Chemokine CXCL10,
pubmed-meshheading:12021306-Chemokines, CXC,
pubmed-meshheading:12021306-Chemokines,
pubmed-meshheading:12021306-Chemokines, CC
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