Source:http://linkedlifedata.com/resource/pubmed/id/15527103
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2004-11-5
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pubmed:abstractText |
Local delivery of cytokines has been shown to have a potent anti-tumor activity against a wide range of malignant brain tumors. In this study, we examined the role of systemic immunosuppression using dexamethasone on the efficacy of local IL-2 immunotherapy in treating experimental murine CNS tumors. An endothelial cell line secreting hIL-2 (NTC-121) was injected intracranially in C57BL/6 mice (n = 10/ group) along with B16/F10 (wild type) melanoma cells. A separate set of animals also received daily injections of either 1 mg/k or 10 mg/kg of dexamethasone. Sixty percent of mice treated with IL-2 (P < 0.001 vs. control) vs. 55% (P < 0.005) of mice treated with IL-2 and 1 mg/kg of dexamethasone were long-term survivors (LTS) of > 120 days. There was no difference in survival between control animals that received only wild type cells or animals that were treated with IL-2 and 10 mg/kg of dexamethasone. Histopathological examination of brains from animals sacrificed at different times showed an accumulation of CD8 + T-cells around the site of the injected tumor only in the IL-2 group and the group that received 1 mg/kg of dexamethasone. These results suggest that while high doses of dexamethasone can completely inhibit the immune response observed with IL-2, lower and more likely therapeutic doses of dexamethasone do not inhibit local IL-2 immunotherapy.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0167-594X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
70
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
23-8
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:15527103-Animals,
pubmed-meshheading:15527103-Brain Neoplasms,
pubmed-meshheading:15527103-CD8-Positive T-Lymphocytes,
pubmed-meshheading:15527103-Dexamethasone,
pubmed-meshheading:15527103-Dose-Response Relationship, Drug,
pubmed-meshheading:15527103-Endothelial Cells,
pubmed-meshheading:15527103-Glucocorticoids,
pubmed-meshheading:15527103-Humans,
pubmed-meshheading:15527103-Immunotherapy,
pubmed-meshheading:15527103-Interleukin-2,
pubmed-meshheading:15527103-Melanoma, Experimental,
pubmed-meshheading:15527103-Mice,
pubmed-meshheading:15527103-Mice, Inbred C57BL,
pubmed-meshheading:15527103-Rats,
pubmed-meshheading:15527103-Skin Neoplasms,
pubmed-meshheading:15527103-Survival Rate,
pubmed-meshheading:15527103-Transplantation, Heterologous
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pubmed:year |
2004
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pubmed:articleTitle |
Dexamethasone mediated inhibition of local IL-2 immunotherapy is dose dependent in experimental brain tumors.
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pubmed:affiliation |
Division of Neurosurgery, The University of Chicago Hospitals, Chicago, IL 60637, USA. mlesniak@surgery.bsd.uchicago.edu
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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