pubmed-article:12882650 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:12882650 | lifeskim:mentions | umls-concept:C0025260 | lld:lifeskim |
pubmed-article:12882650 | lifeskim:mentions | umls-concept:C1332717 | lld:lifeskim |
pubmed-article:12882650 | lifeskim:mentions | umls-concept:C1706438 | lld:lifeskim |
pubmed-article:12882650 | lifeskim:mentions | umls-concept:C0039194 | lld:lifeskim |
pubmed-article:12882650 | lifeskim:mentions | umls-concept:C0301944 | lld:lifeskim |
pubmed-article:12882650 | lifeskim:mentions | umls-concept:C0085358 | lld:lifeskim |
pubmed-article:12882650 | lifeskim:mentions | umls-concept:C1413244 | lld:lifeskim |
pubmed-article:12882650 | lifeskim:mentions | umls-concept:C2698600 | lld:lifeskim |
pubmed-article:12882650 | lifeskim:mentions | umls-concept:C0449295 | lld:lifeskim |
pubmed-article:12882650 | lifeskim:mentions | umls-concept:C0302350 | lld:lifeskim |
pubmed-article:12882650 | pubmed:dateCreated | 2004-5-10 | lld:pubmed |
pubmed-article:12882650 | pubmed:abstractText | Adoptive immunotherapy with cytotoxic T lymphocytes (CTL) represents an alternative approach to treating solid tumors. Ideally, this would confer long-term protection against tumor. We previously demonstrated that in vitro-generated tumor-specific CTL from the ovalbumin (OVA)-specific OT-I T cell receptor transgenic mouse persisted long after adoptive transfer as memory T cells. When recipient mice were challenged with the OVA-expressing E.G7 thymoma, tumor growth was delayed and sometimes prevented. The reasons for therapeutic failures were not clear. | lld:pubmed |
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pubmed-article:12882650 | pubmed:language | eng | lld:pubmed |
pubmed-article:12882650 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12882650 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:12882650 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12882650 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:12882650 | pubmed:month | Jul | lld:pubmed |
pubmed-article:12882650 | pubmed:issn | 1471-2407 | lld:pubmed |
pubmed-article:12882650 | pubmed:author | pubmed-author:MalekThomas... | lld:pubmed |
pubmed-article:12882650 | pubmed:author | pubmed-author:BatheOliver... | lld:pubmed |
pubmed-article:12882650 | pubmed:author | pubmed-author:Dalyot-Herman... | lld:pubmed |
pubmed-article:12882650 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:12882650 | pubmed:day | 28 | lld:pubmed |
pubmed-article:12882650 | pubmed:volume | 3 | lld:pubmed |
pubmed-article:12882650 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:12882650 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:12882650 | pubmed:pagination | 21 | lld:pubmed |
pubmed-article:12882650 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:12882650 | pubmed:year | 2003 | lld:pubmed |
pubmed-article:12882650 | pubmed:articleTitle | Therapeutic limitations in tumor-specific CD8+ memory T cell engraftment. | lld:pubmed |
pubmed-article:12882650 | pubmed:affiliation | Department of Surgery, University of Calgary, Calgary, AB, Canada. bathe@ucalgary.ca | lld:pubmed |
pubmed-article:12882650 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:12882650 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:12882650 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |