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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2002-10-14
pubmed:abstractText
Interleukin (IL)-12, especially in the presence of neutralizing anti-IL-4 monoclonal antibodies, primed CD45RO(-) T clones for high CCL3/macrophage-inflammatory protein-1alpha (MIP-1alpha) and CCL4/MIP-1beta levels. In CD4(+) and CD8(+) clones from two patients deficient for IL-12Rbeta1 (IL-12Rbeta1(-/-)), production of CCL3/MIP-1alpha and CCL4/MIP-1beta was defective. CD4(+) clones from two patients deficient for interferon-gamma (IFN-gamma) R1 (IFN-gammaR1(-/-)) produced somewhat decreased CCL4/MIP-1beta levels. IL-12 failed to prime CD4(+) or CD8(+) healthy clones for high CCL5/regulated on activation, normal T expressed and secreted (RANTES) production, although its secretion was impaired in CD4(+) clones from IL-12Rbeta1(-/-) and IFN-gammaR1(-/-) patients. CCR5 surface expression was up-regulated in resting peripheral blood mononuclear cells and CD4(+) clones from both kinds of patients, rendering them more susceptible to CCR5-dependent (R5) HIV-1 infection. Neutralization of IFN-gamma increased CCR5 expression and decreased CC-chemokine secretion by CD4(+) clones from healthy and IL-12Rbeta1(-/-) individuals, suggesting an IFN-gamma-dependent control of CCR5 expression. These data provide the first documented analysis of chemokine secretion and chemokine receptor expression on T cells from IL-12 and IFN-gamma receptor-deficient patients and dissect the role of IL-12 and IFN-gamma on inducing inflammatory chemokine secretion and down-regulating CCR5 expression in human T cells.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD4, http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD45, http://linkedlifedata.com/resource/pubmed/chemical/Chemokine CCL3, http://linkedlifedata.com/resource/pubmed/chemical/Chemokine CCL4, http://linkedlifedata.com/resource/pubmed/chemical/Chemokine CCL5, http://linkedlifedata.com/resource/pubmed/chemical/Chemokines, CC, http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma, http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-12, http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-4, http://linkedlifedata.com/resource/pubmed/chemical/Macrophage Inflammatory Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, CCR5, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Interferon, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Interleukin, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Interleukin-12, http://linkedlifedata.com/resource/pubmed/chemical/interferon gamma receptor
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0741-5400
pubmed:author
pubmed:issnType
Print
pubmed:volume
72
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
735-42
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:12377943-Antigens, CD4, pubmed-meshheading:12377943-Antigens, CD45, pubmed-meshheading:12377943-CD4-Positive T-Lymphocytes, pubmed-meshheading:12377943-CD8-Positive T-Lymphocytes, pubmed-meshheading:12377943-Cells, Cultured, pubmed-meshheading:12377943-Chemokine CCL3, pubmed-meshheading:12377943-Chemokine CCL4, pubmed-meshheading:12377943-Chemokine CCL5, pubmed-meshheading:12377943-Chemokines, CC, pubmed-meshheading:12377943-Down-Regulation, pubmed-meshheading:12377943-Gene Expression, pubmed-meshheading:12377943-HIV Infections, pubmed-meshheading:12377943-HIV-1, pubmed-meshheading:12377943-Humans, pubmed-meshheading:12377943-Interferon-gamma, pubmed-meshheading:12377943-Interleukin-12, pubmed-meshheading:12377943-Interleukin-4, pubmed-meshheading:12377943-Macrophage Inflammatory Proteins, pubmed-meshheading:12377943-Receptors, CCR5, pubmed-meshheading:12377943-Receptors, Interferon, pubmed-meshheading:12377943-Receptors, Interleukin, pubmed-meshheading:12377943-Receptors, Interleukin-12, pubmed-meshheading:12377943-Virus Replication
pubmed:year
2002
pubmed:articleTitle
IFN-gamma and IL-12 differentially regulate CC-chemokine secretion and CCR5 expression in human T lymphocytes.
pubmed:affiliation
Department of Clinical and Biological Sciences, University of Turin, Orbassano, Italy.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't