Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7
pubmed:dateCreated
1996-9-20
pubmed:abstractText
IL-15 is a newly identified cytokine that has T cell and B cell growth factor activity similar to that of IL-2. In this study, a novel biologic function of IL-15 to promote cytokine production by human Th cells has been elucidated. Dermatophagoides farinae 11 (a major allergen of house dust mite)-specific human T cell clones produced IL-5 in response to recombinant human IL-15 as well as to either anti-CD3 or IL-2 stimulation. IL-5 mRNA became detectable 3 h after IL-15 stimulation and reached a maximum at 9 h. Human IL-5 promoter/enhancer-luciferase gene construct transfected to T cell clones was clearly transcribed in response to IL-15, indicating that the approximately 500-bp human IL-5 promoter/enhancer segment 5' upstream of the coding region sufficiently responded to IL-15. IL-15-induced IL-5 synthesis was completely inhibited by the tyrosine kinase inhibitor, herbimycin A, suggesting the involvement of tyrosine kinases in the signal transduction leading to IL-5 synthesis as well as to proliferation of T cells induced by IL-15. Whereas IL-5 production by human peripheral T cells was abolished by the addition of anti-IL-2-neutralizing Abs into the culture, IL-15 restored the IL-5 synthesis despite effective IL-2 neutralization. IL-15 produced at the site of allergic inflammation may play a role in the recruitment and activation of eosinophils by inducing IL-5 (a Th2 cytokine) production by T cells.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Actins, http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, http://linkedlifedata.com/resource/pubmed/chemical/Benzoquinones, http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers, http://linkedlifedata.com/resource/pubmed/chemical/Enzyme Inhibitors, http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-15, http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-2, http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-5, http://linkedlifedata.com/resource/pubmed/chemical/Interleukins, http://linkedlifedata.com/resource/pubmed/chemical/Lactams, Macrocyclic, http://linkedlifedata.com/resource/pubmed/chemical/Protein-Tyrosine Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Quinones, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Interleukin-2, http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins, http://linkedlifedata.com/resource/pubmed/chemical/herbimycin
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0022-1767
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
156
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2400-5
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:8786297-Actins, pubmed-meshheading:8786297-Antibodies, pubmed-meshheading:8786297-Base Sequence, pubmed-meshheading:8786297-Benzoquinones, pubmed-meshheading:8786297-Clone Cells, pubmed-meshheading:8786297-DNA Primers, pubmed-meshheading:8786297-Enhancer Elements, Genetic, pubmed-meshheading:8786297-Enzyme Inhibitors, pubmed-meshheading:8786297-Gene Expression, pubmed-meshheading:8786297-Humans, pubmed-meshheading:8786297-Interleukin-15, pubmed-meshheading:8786297-Interleukin-2, pubmed-meshheading:8786297-Interleukin-5, pubmed-meshheading:8786297-Interleukins, pubmed-meshheading:8786297-Lactams, Macrocyclic, pubmed-meshheading:8786297-Molecular Sequence Data, pubmed-meshheading:8786297-Plasmids, pubmed-meshheading:8786297-Promoter Regions, Genetic, pubmed-meshheading:8786297-Protein-Tyrosine Kinases, pubmed-meshheading:8786297-Quinones, pubmed-meshheading:8786297-Receptors, Interleukin-2, pubmed-meshheading:8786297-Recombinant Proteins, pubmed-meshheading:8786297-T-Lymphocytes, Helper-Inducer, pubmed-meshheading:8786297-Transfection
pubmed:year
1996
pubmed:articleTitle
IL-15 promotes cytokine production of human T helper cells.
pubmed:affiliation
Departments of Medicine, Faculty of Medicine, University of Tokyo, Japan.
pubmed:publicationType
Journal Article