| pubmed-article:15803149 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:15803149 | lifeskim:mentions | umls-concept:C0006826 | lld:lifeskim |
| pubmed-article:15803149 | lifeskim:mentions | umls-concept:C0011306 | lld:lifeskim |
| pubmed-article:15803149 | lifeskim:mentions | umls-concept:C0301521 | lld:lifeskim |
| pubmed-article:15803149 | pubmed:issue | 4 | lld:pubmed |
| pubmed-article:15803149 | pubmed:dateCreated | 2005-4-1 | lld:pubmed |
| pubmed-article:15803149 | pubmed:abstractText | Mouse studies have shown that the immune system can reject tumours, and the identification of tumour antigens that can be recognized by human T cells has facilitated the development of immunotherapy protocols. Vaccines against cancer aim to induce tumour-specific effector T cells that can reduce the tumour mass, as well as tumour-specific memory T cells that can control tumour relapse. Owing to their capacity to regulate T-cell immunity, dendritic cells are increasingly used as adjuvants for vaccination, and the immunogenicity of antigens delivered by dendritic cells has now been shown in patients with cancer. A better understanding of how dendritic cells regulate immune responses will allow us to better exploit these cells to induce effective antitumour immunity. | lld:pubmed |
| pubmed-article:15803149 | pubmed:language | eng | lld:pubmed |
| pubmed-article:15803149 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15803149 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:15803149 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15803149 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15803149 | pubmed:month | Apr | lld:pubmed |
| pubmed-article:15803149 | pubmed:issn | 1474-1733 | lld:pubmed |
| pubmed-article:15803149 | pubmed:author | pubmed-author:BanchereauJac... | lld:pubmed |
| pubmed-article:15803149 | pubmed:author | pubmed-author:PaluckaA... | lld:pubmed |
| pubmed-article:15803149 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:15803149 | pubmed:volume | 5 | lld:pubmed |
| pubmed-article:15803149 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:15803149 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:15803149 | pubmed:pagination | 296-306 | lld:pubmed |
| pubmed-article:15803149 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
| pubmed-article:15803149 | pubmed:meshHeading | pubmed-meshheading:15803149... | lld:pubmed |
| pubmed-article:15803149 | pubmed:meshHeading | pubmed-meshheading:15803149... | lld:pubmed |
| pubmed-article:15803149 | pubmed:meshHeading | pubmed-meshheading:15803149... | lld:pubmed |
| pubmed-article:15803149 | pubmed:meshHeading | pubmed-meshheading:15803149... | lld:pubmed |
| pubmed-article:15803149 | pubmed:meshHeading | pubmed-meshheading:15803149... | lld:pubmed |
| pubmed-article:15803149 | pubmed:year | 2005 | lld:pubmed |
| pubmed-article:15803149 | pubmed:articleTitle | Dendritic cells as therapeutic vaccines against cancer. | lld:pubmed |
| pubmed-article:15803149 | pubmed:affiliation | Baylor Institute for Immunology Research, 3434 Live Oak, Dallas, Texas 75204, USA. jacquesb@baylorhealth.edu | lld:pubmed |
| pubmed-article:15803149 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:15803149 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:15803149 | pubmed:publicationType | Review | lld:pubmed |
| pubmed-article:15803149 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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