Source:http://linkedlifedata.com/resource/pubmed/id/18425373
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2008-4-21
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pubmed:abstractText |
Many studies have demonstrated that interleukin 15 (IL-15) is a cytokine with strong antitumor properties and have suggested its potential use in tumor immunotherapy. IL-15 exerts its effect on innate and acquired immunity with the most prominent action in NK cells and CD8(+) memory T cells. Therefore, many authors have proposed that IL-15 could be a good candidate for augmenting the efficacy of vaccination strategies. In our experiments, in a model of B78-H1 murine transplantable melanoma, tumor-bearing mice were treated with different cytokine-gene modified tumor cell vaccines (producing TNF-alpha, GM-CSF, IL-12 or IL-6/sIL-6R) followed by a series of IL-15 injections. In order to investigate the infiltration of treated tumors by leukocytes, immunohistochemical staining was performed. In every case, the combined therapy was superior to the treatment with either a vaccine or IL-15 alone. Tumors treated with the combination of B78-H1 melanoma cells secreting IL-12 (B78/IL-12 vaccine) and IL-15 were heavily infiltrated by granulocytes. IL-15, either alone or in combination with the B78/IL-12 vaccine, influenced infiltration of tumors with CD3(+) lymphocytes, CD4(+)and CD8(+). To our knowledge, this is the first report that shows the universal genetically-modified tumor cell vaccine-augmenting properties of IL-15. The cytokine can be useful as an adjuvant in cancer gene therapy in humans.
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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, CD3,
http://linkedlifedata.com/resource/pubmed/chemical/Antineoplastic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Cancer Vaccines,
http://linkedlifedata.com/resource/pubmed/chemical/Cytokines,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-15
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
1021-335X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
19
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1173-9
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pubmed:meshHeading |
pubmed-meshheading:18425373-Animals,
pubmed-meshheading:18425373-Antigens, CD3,
pubmed-meshheading:18425373-Antineoplastic Agents,
pubmed-meshheading:18425373-CD4-Positive T-Lymphocytes,
pubmed-meshheading:18425373-CD8-Positive T-Lymphocytes,
pubmed-meshheading:18425373-Cancer Vaccines,
pubmed-meshheading:18425373-Cytokines,
pubmed-meshheading:18425373-Disease Models, Animal,
pubmed-meshheading:18425373-Interleukin-15,
pubmed-meshheading:18425373-Melanoma,
pubmed-meshheading:18425373-Mice,
pubmed-meshheading:18425373-Mice, Inbred C57BL,
pubmed-meshheading:18425373-Mice, Inbred DBA,
pubmed-meshheading:18425373-Neoplasm Transplantation,
pubmed-meshheading:18425373-Time Factors
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pubmed:year |
2008
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pubmed:articleTitle |
Interleukin 15 augments antitumor activity of cytokine gene-modified melanoma cell vaccines in a murine model.
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pubmed:affiliation |
Department of Immunology, Centre of Biostructure Research, Medical University of Warsaw, 02-097 Warsaw, Poland.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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