pubmed-article:17145892 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:17145892 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
pubmed-article:17145892 | lifeskim:mentions | umls-concept:C0037047 | lld:lifeskim |
pubmed-article:17145892 | lifeskim:mentions | umls-concept:C1332717 | lld:lifeskim |
pubmed-article:17145892 | lifeskim:mentions | umls-concept:C1706438 | lld:lifeskim |
pubmed-article:17145892 | lifeskim:mentions | umls-concept:C0039194 | lld:lifeskim |
pubmed-article:17145892 | lifeskim:mentions | umls-concept:C1282910 | lld:lifeskim |
pubmed-article:17145892 | lifeskim:mentions | umls-concept:C0085358 | lld:lifeskim |
pubmed-article:17145892 | lifeskim:mentions | umls-concept:C1704632 | lld:lifeskim |
pubmed-article:17145892 | lifeskim:mentions | umls-concept:C0871261 | lld:lifeskim |
pubmed-article:17145892 | lifeskim:mentions | umls-concept:C1413244 | lld:lifeskim |
pubmed-article:17145892 | lifeskim:mentions | umls-concept:C2698600 | lld:lifeskim |
pubmed-article:17145892 | lifeskim:mentions | umls-concept:C2911692 | lld:lifeskim |
pubmed-article:17145892 | lifeskim:mentions | umls-concept:C1706817 | lld:lifeskim |
pubmed-article:17145892 | lifeskim:mentions | umls-concept:C0439859 | lld:lifeskim |
pubmed-article:17145892 | lifeskim:mentions | umls-concept:C1707455 | lld:lifeskim |
pubmed-article:17145892 | lifeskim:mentions | umls-concept:C1533691 | lld:lifeskim |
pubmed-article:17145892 | lifeskim:mentions | umls-concept:C1515895 | lld:lifeskim |
pubmed-article:17145892 | lifeskim:mentions | umls-concept:C1708943 | lld:lifeskim |
pubmed-article:17145892 | pubmed:issue | 23 | lld:pubmed |
pubmed-article:17145892 | pubmed:dateCreated | 2006-12-5 | lld:pubmed |
pubmed-article:17145892 | pubmed:abstractText | Allogeneic cell therapy as a means to break immunotolerance to solid tumors is increasingly used for cancer treatment. To investigate cellular alloimmune responses in a human tumor model, primary cultures were established from renal cell carcinoma (RCC) tissues of 56 patients. In three patients with stable RCC line and human leukocyte antigen (HLA)-identical sibling donor available, allogeneic and autologous RCC reactivities were compared using mixed lymphocyte/tumor cell cultures (MLTC). Responding lymphocytes were exclusively CD8(+) T cells, whereas CD4(+) T cells or natural killer cells were never observed. Sibling MLTC populations showed higher proliferative and cytolytic antitumor responses compared with their autologous counterparts. The allo-MLTC responders originated from the CD8(+) CD62L(high)(+) peripheral blood subpopulation containing naive precursor and central memory T cells. Limiting dilution cloning failed to establish CTL clones from autologous MLTCs or tumor-infiltrating lymphocytes. In contrast, a broad panel of RCC-reactive CTL clones was expanded from each allogeneic MLTC. These sibling CTL clones either recognized exclusively the original RCC tumor line or cross-reacted with nonmalignant kidney cells of patient origin. A minority of CTL clones also recognized patient-derived hematopoietic cells or other allogeneic tumor targets. The MHC-restricting alleles for RCC-reactive sibling CTL clones included HLA-A2, HLA-A3, HLA-A11, HLA-A24, and HLA-B7. In one sibling donor-RCC pair, strongly proliferative CD3(+)CD16(+)CD57(+) CTL clones with non-HLA-restricted antitumor reactivity were established. Our results show superior tumor-reactive CD8 responses of matched allogeneic compared with autologous T cells. These data encourage the generation of antitumor T-cell products from HLA-identical siblings and their potential use in adoptive immunotherapy of metastatic RCC patients. | lld:pubmed |
pubmed-article:17145892 | pubmed:language | eng | lld:pubmed |
pubmed-article:17145892 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17145892 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:17145892 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17145892 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17145892 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17145892 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17145892 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17145892 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:17145892 | pubmed:month | Dec | lld:pubmed |
pubmed-article:17145892 | pubmed:issn | 0008-5472 | lld:pubmed |
pubmed-article:17145892 | pubmed:author | pubmed-author:HerrWolfgangW | lld:pubmed |
pubmed-article:17145892 | pubmed:author | pubmed-author:HuberChristop... | lld:pubmed |
pubmed-article:17145892 | pubmed:author | pubmed-author:FalkChristine... | lld:pubmed |
pubmed-article:17145892 | pubmed:author | pubmed-author:BrennerWalbur... | lld:pubmed |
pubmed-article:17145892 | pubmed:author | pubmed-author:RanieriElenaE | lld:pubmed |
pubmed-article:17145892 | pubmed:author | pubmed-author:MelchiorSebas... | lld:pubmed |
pubmed-article:17145892 | pubmed:author | pubmed-author:StrandSusanne... | lld:pubmed |
pubmed-article:17145892 | pubmed:author | pubmed-author:NonnMarionM | lld:pubmed |
pubmed-article:17145892 | pubmed:author | pubmed-author:MeyerRalfR | lld:pubmed |
pubmed-article:17145892 | pubmed:author | pubmed-author:SchnürerElkeE | lld:pubmed |
pubmed-article:17145892 | pubmed:author | pubmed-author:LennerzVolker... | lld:pubmed |
pubmed-article:17145892 | pubmed:author | pubmed-author:WehlerThomasT | lld:pubmed |
pubmed-article:17145892 | pubmed:author | pubmed-author:GröneMarkM | lld:pubmed |
pubmed-article:17145892 | pubmed:author | pubmed-author:KauscheSandra... | lld:pubmed |
pubmed-article:17145892 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:17145892 | pubmed:day | 1 | lld:pubmed |
pubmed-article:17145892 | pubmed:volume | 66 | lld:pubmed |
pubmed-article:17145892 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:17145892 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:17145892 | pubmed:pagination | 11447-54 | lld:pubmed |
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pubmed-article:17145892 | pubmed:year | 2006 | lld:pubmed |
pubmed-article:17145892 | pubmed:articleTitle | Superior antitumor in vitro responses of allogeneic matched sibling compared with autologous patient CD8+ T cells. | lld:pubmed |
pubmed-article:17145892 | pubmed:affiliation | Department of Medicine III, Hematology and Oncology, University of Mainz, Mainz, Germany. | lld:pubmed |
pubmed-article:17145892 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:17145892 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:17145892 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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