Source:http://linkedlifedata.com/resource/pubmed/id/11115616
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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0007097,
umls-concept:C0021344,
umls-concept:C0027651,
umls-concept:C0030956,
umls-concept:C0042210,
umls-concept:C0087111,
umls-concept:C0312740,
umls-concept:C0439640,
umls-concept:C0871261,
umls-concept:C1533691,
umls-concept:C1704632,
umls-concept:C1706817,
umls-concept:C1881488,
umls-concept:C1883254,
umls-concept:C1947910,
umls-concept:C2911692
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pubmed:issue |
1
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pubmed:dateCreated |
2000-12-29
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pubmed:abstractText |
Murine carcinoma induced by MK 16 cells expressing HPV 16 E6/E7 oncogenes was utilized to examine the therapeutic effect of dendritic cell-based tumour vaccines. Mice carrying 5-day MK 16 tumours were injected peritumorally with either dendritic cells (DC) or DC pulsed with MK 16 tumour lysate. Both the unpulsed and MK 16 lysate-pulsed DC vaccines inhibited growth of the MK 16 transplants, the pulsed DC being more efficient than the unpulsed vaccines. In vitro priming of the effector cell-mediated anti-MK 16 responses by DC pulsed with MK 16 tumour lysate and a synthetic HPV 16 E7(49-57) peptide RAHYNIVTF was compared. The priming activity of the lysate was substantially higher than that of the HPV 16 E7(49-57) peptide; the priming activity was similar to that of a standard moderately immunogenic chemically-induced sarcoma. Taken collectively, these results suggest that DC vaccines pulsed with HPV 16-associated tumour lysates represent a prospective modality for treatment of HPV 16-associated carcinomas.
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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 |
Jan
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pubmed:issn |
1107-3756
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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 |
97-100
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11115616-Amino Acid Sequence,
pubmed-meshheading:11115616-Animals,
pubmed-meshheading:11115616-Cancer Vaccines,
pubmed-meshheading:11115616-Dendritic Cells,
pubmed-meshheading:11115616-Humans,
pubmed-meshheading:11115616-Immunotherapy, Adoptive,
pubmed-meshheading:11115616-Mice,
pubmed-meshheading:11115616-Mice, Inbred C57BL,
pubmed-meshheading:11115616-Papillomaviridae,
pubmed-meshheading:11115616-Papillomavirus Infections,
pubmed-meshheading:11115616-Papillomavirus Vaccines,
pubmed-meshheading:11115616-Peptides,
pubmed-meshheading:11115616-Spleen,
pubmed-meshheading:11115616-Tumor Cells, Cultured,
pubmed-meshheading:11115616-Tumor Virus Infections,
pubmed-meshheading:11115616-Vaccines, Synthetic
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pubmed:year |
2001
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pubmed:articleTitle |
Therapy of HPV 16-associated carcinoma with dendritic cell-based vaccines: in vitro priming of the effector cell responses by DC pulsed with tumour lysates and synthetic RAHYNIVTF peptide.
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pubmed:affiliation |
Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, 166 37 Prague 6, Czech Republic. indrova@img.cas.cz
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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