Source:http://linkedlifedata.com/resource/pubmed/id/15856455
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2005-8-3
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pubmed:abstractText |
T cell infiltration in colorectal cancer is associated with a favorable prognosis, suggesting an occurrence of a certain degree of anti-tumor immunity. T helper type 1 (Th1) and Th2 cells are now known to selectively express CC-chemokine receptor 5 (CCR5)/CXC-chemokine receptor 3 (CXCR3) and CCR4, respectively. To clarify the mechanism of T cell infiltration, we examined in situ expression of these chemokine receptors and their respective chemokine ligands in 40 cases of human colorectal cancer. Immunohistochemistry showed a predominant accumulation of T cells expressing CCR5 and CXCR3 mainly along the invasive margin, whereas those expressing CCR4 were rare. Flow cytometric analysis showed that more than half of CD8(+) T cells and a fraction of CD4(+) cells isolated from fresh tumor tissues co-expressed CCR5 and CXCR3, and CD8(+) T cells and CD4(+) cells predominantly produced interferon-gamma (IFN-gamma) over interleukin-4 (IL-4) after in vitro stimulation. RANTES/CCL5, a ligand of CCR5, was localized within infiltrating CD8(+) T cells in a granular pattern, whereas IP-10/CXCL10, a ligand of CXCR3, was localized in cancer cells and macrophages along the invasive margin. These data were consistent with an active recruitment of T cells expressing CCR5 or CXCR3 into the invasive margin of colorectal cancer. With the previous clinicopathological studies showing a favorable prognostic impact of T cell infiltration in colorectal cancer, our study supports the occurrence of a certain level of Th1-shifted cellular immune responses in human colorectal cancer.
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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/CXCR3 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Chemokines,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, CCR5,
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 |
Oct
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pubmed:issn |
0020-7136
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
10
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pubmed:volume |
116
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
949-56
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:15856455-Adult,
pubmed-meshheading:15856455-Aged,
pubmed-meshheading:15856455-Aged, 80 and over,
pubmed-meshheading:15856455-Chemokines,
pubmed-meshheading:15856455-Colorectal Neoplasms,
pubmed-meshheading:15856455-Flow Cytometry,
pubmed-meshheading:15856455-Gene Expression Regulation, Neoplastic,
pubmed-meshheading:15856455-Humans,
pubmed-meshheading:15856455-Intestinal Mucosa,
pubmed-meshheading:15856455-Lymphocytes, Tumor-Infiltrating,
pubmed-meshheading:15856455-Middle Aged,
pubmed-meshheading:15856455-Receptors, CCR5,
pubmed-meshheading:15856455-Receptors, CXCR3,
pubmed-meshheading:15856455-Receptors, Chemokine,
pubmed-meshheading:15856455-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:15856455-T-Lymphocytes
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pubmed:year |
2005
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pubmed:articleTitle |
Selective infiltration of CCR5(+)CXCR3(+) T lymphocytes in human colorectal carcinoma.
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pubmed:affiliation |
Department of Surgery, Tohoku University School of Medicine, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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