Source:http://linkedlifedata.com/resource/pubmed/id/10975677
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
2000-12-4
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pubmed:abstractText |
Using a novel cationic lipid delivery system consisting of N-[1-(2,3-dioleoyloxy)propyl]-N,N,N-trimethylammonium chloride and cholesterol, we delivered murine interleukin-2 (IL-2) cDNA directly into an established murine renal cell carcinoma (Renca). Production of IL-2 within the tumor induced rejection of established tumors (62% on average), whereas control plasmid had little or no effect (17% on average). Surviving animals treated with IL-2:lipid were highly resistant to Renca rechallenge, but not to cross-challenge with a syngeneic mammary adenocarcinoma. Experiments on selectively immunosuppressed animals indicated a requirement for CD8+ T, natural killer, and polymorphonuclear cells. By contrast, depletion of CD4+ T cells did not disrupt the ability of IL-2:lipid to induce tumor rejection. A combination of IL-2 gene therapy with 5-fluorouracil treatment increased the antitumoral efficacy and survival of mice bearing primary and metastatic Renca tumors (42% survival with IL-2:lipid compared with 94% survival with IL-2:lipid plus 5-fluorouracil). These data indicate that rejection of primary and metastatic tumors can be achieved after intratumoral delivery of a nonviral IL-2 gene therapy, and is increased in combination with systemic delivery of a conventional chemotherapeutic agent.
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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/DNA, Complementary,
http://linkedlifedata.com/resource/pubmed/chemical/Fluorouracil,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-2,
http://linkedlifedata.com/resource/pubmed/chemical/N-(1-(2,3-dioleyloxy)propyl)-N,N,N-t...,
http://linkedlifedata.com/resource/pubmed/chemical/Quaternary Ammonium Compounds
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0929-1903
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
7
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1165-71
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pubmed:dateRevised |
2005-11-17
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pubmed:meshHeading |
pubmed-meshheading:10975677-Animals,
pubmed-meshheading:10975677-Carcinoma, Renal Cell,
pubmed-meshheading:10975677-Combined Modality Therapy,
pubmed-meshheading:10975677-DNA, Complementary,
pubmed-meshheading:10975677-Female,
pubmed-meshheading:10975677-Fluorouracil,
pubmed-meshheading:10975677-Gene Therapy,
pubmed-meshheading:10975677-Interleukin-2,
pubmed-meshheading:10975677-Kidney Neoplasms,
pubmed-meshheading:10975677-Mice,
pubmed-meshheading:10975677-Mice, Inbred BALB C,
pubmed-meshheading:10975677-Quaternary Ammonium Compounds
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pubmed:year |
2000
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pubmed:articleTitle |
Antitumoral effect of a nonviral interleukin-2 gene therapy is enhanced by combination with 5-fluorouracil.
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pubmed:affiliation |
Valentis, Inc., The Woodlands, Texas 77381-4248, USA.
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pubmed:publicationType |
Journal Article
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