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http://purl.uniprot.org/citations/11280764http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/11280764http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/11280764http://www.w3.org/2000/01/rdf-schema#comment"Pancreatic cancer continues to be a major unsolved health problem in the world. The prognosis of pancreatic cancer is extremely poor with a median survival of 3-4 months and the 5-year survival being 1-4%. This poor prognosis is primarily because of a lack of effective therapies, and thus development of new treatment modalities is needed. One of these treatments could involve specific immunotherapy, for which elucidation off the molecular basis of T cell-mediated recognition of cancer cells is required. We report here six different genes and 19 immunogenic epitopes from pancreatic adenocarcinoma cells and T-cell receptor beta usage of HLA-A2-restricted CTL clones reacting to some of these epitopes. Sixteen of 19 epitopes were found to possess the ability to induce HLA-A2-restricted CTL activity in the peripheral blood lymphocytes of patients with pancreatic and also colon adenocarcinomas. These results should provide a scientific basis for the development of specific immunotherapy for pancreatic and colon cancer patients."xsd:string
http://purl.uniprot.org/citations/11280764http://purl.uniprot.org/core/author"Itoh K."xsd:string
http://purl.uniprot.org/citations/11280764http://purl.uniprot.org/core/author"Itoh K."xsd:string
http://purl.uniprot.org/citations/11280764http://purl.uniprot.org/core/author"Ito M."xsd:string
http://purl.uniprot.org/citations/11280764http://purl.uniprot.org/core/author"Ito M."xsd:string
http://purl.uniprot.org/citations/11280764http://purl.uniprot.org/core/author"Saito N."xsd:string
http://purl.uniprot.org/citations/11280764http://purl.uniprot.org/core/author"Saito N."xsd:string
http://purl.uniprot.org/citations/11280764http://purl.uniprot.org/core/author"Harashima N."xsd:string
http://purl.uniprot.org/citations/11280764http://purl.uniprot.org/core/author"Harashima N."xsd:string
http://purl.uniprot.org/citations/11280764http://purl.uniprot.org/core/author"Ochi M."xsd:string
http://purl.uniprot.org/citations/11280764http://purl.uniprot.org/core/author"Ochi M."xsd:string
http://purl.uniprot.org/citations/11280764http://purl.uniprot.org/core/author"Shichijo S."xsd:string
http://purl.uniprot.org/citations/11280764http://purl.uniprot.org/core/author"Shichijo S."xsd:string
http://purl.uniprot.org/citations/11280764http://purl.uniprot.org/core/author"Tsuda N."xsd:string
http://purl.uniprot.org/citations/11280764http://purl.uniprot.org/core/author"Tsuda N."xsd:string
http://purl.uniprot.org/citations/11280764http://purl.uniprot.org/core/date"2001"xsd:gYear
http://purl.uniprot.org/citations/11280764http://purl.uniprot.org/core/date"2001"xsd:gYear
http://purl.uniprot.org/citations/11280764http://purl.uniprot.org/core/name"Cancer Res."xsd:string
http://purl.uniprot.org/citations/11280764http://purl.uniprot.org/core/name"Cancer Res."xsd:string
http://purl.uniprot.org/citations/11280764http://purl.uniprot.org/core/pages"2038-2046"xsd:string
http://purl.uniprot.org/citations/11280764http://purl.uniprot.org/core/pages"2038-2046"xsd:string
http://purl.uniprot.org/citations/11280764http://purl.uniprot.org/core/title"Molecular basis of T cell-mediated recognition of pancreatic cancer cells."xsd:string
http://purl.uniprot.org/citations/11280764http://purl.uniprot.org/core/title"Molecular basis of T cell-mediated recognition of pancreatic cancer cells."xsd:string