Source:http://linkedlifedata.com/resource/pubmed/id/11506745
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
2001-8-16
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pubmed:abstractText |
Targets of cyclosporine (CsA) were identified from an array of stimulated lymphocyte responses (sLR) comprising 34 stimulation conditions in whole blood from 3 normal human volunteers (NHV) containing clinically relevant CsA concentrations (0-1200 ng/ml) in vitro. In whole blood from 5 additional NHV, selected targets (intracellular interleukin-2 [IL-2], tumor-necrosis factor-alpha [TNF-alpha], and interferon-gamma [IFN-gamma]) were measured in phorbol myristate acetate (PMA)-ionomycin-stimulated T lymphocytes. Effect:concentration relationships were analyzed with E(max) pharmacodynamic (PD) equations and expressed as the concentration associated with one-half maximal inhibitory effect (EC(50)). CsA demonstrated a rich matrix of inhibitory effects on T cells (CD3(+)), B cells (CD19(+)), dendritic cells (DC) (CD11c(+)), and basophils (CD123(+)) but not on monocytes (CD14(+)) (n = 3). PD analyses suggested that the EC(50) of CsA (1) for IL-2 in CD3(+) cells in NHV (n = 8) was similar to the EC(50) demonstrated by us previously in CD4(+) cells from transplanted patients (n = 13) (EC(50) = 260 ng/ml vs. 249 ng/ml), (2) for each cytokine was different under identical stimulation conditions (TNF-alpha, 324 ng/ml; IFN-gamma, 504 ng/ml), and (3) was relatively constant for a given cytokine under different stimulation conditions (e.g., PMA-ionomycin or the staphylococcal enterotoxin B [SEB] superantigen). In conclusion, inhibition of cytokine targets by CsA is concentration dependent. Further, a given CsA concentration may produce similar inhibitory effects across different stimulation conditions. Measurement of cytokine target expression may, therefore, allow effect-controlled administration of CsA during clinical transplantation.
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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/Antigens, Differentiation...,
http://linkedlifedata.com/resource/pubmed/chemical/Biological Markers,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclosporine,
http://linkedlifedata.com/resource/pubmed/chemical/Cytokines,
http://linkedlifedata.com/resource/pubmed/chemical/Immunosuppressive Agents
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
1079-9907
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
21
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
507-14
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:11506745-Adult,
pubmed-meshheading:11506745-Antigens, Differentiation, B-Lymphocyte,
pubmed-meshheading:11506745-B-Lymphocytes,
pubmed-meshheading:11506745-Basophils,
pubmed-meshheading:11506745-Biological Markers,
pubmed-meshheading:11506745-Cyclosporine,
pubmed-meshheading:11506745-Cytokines,
pubmed-meshheading:11506745-Dendritic Cells,
pubmed-meshheading:11506745-Humans,
pubmed-meshheading:11506745-Immunosuppressive Agents,
pubmed-meshheading:11506745-Lymphocyte Activation,
pubmed-meshheading:11506745-T-Lymphocytes
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pubmed:year |
2001
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pubmed:articleTitle |
Cytokines and cell surface receptors as target end points of immunosuppression with cyclosporine A.
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pubmed:affiliation |
Children's Hospital of Pittsburgh, Pittsburgh, PA 15213, USA. sindhir@chplink.chp.edu
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pubmed:publicationType |
Journal Article
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