Source:http://linkedlifedata.com/resource/pubmed/id/10495433
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1999-10-21
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pubmed:abstractText |
The identification of tumor-associated antigens has led to increased interest in vaccination strategies to treat and/or prevent cancer. This study examined the feasibility of active-specific immunotherapy against the breast-tumor antigen HER-2/neu using a HER-2/neu transgenic (rNeu-TG) mouse model. rNeu-TG mice develop spontaneous breast tumors after pregnancy, indicating that they fail to mount an effective immune response against rNeu. Allogeneic fibroblasts expressing HER-2/neu were used as a cell-based vaccine. Vaccination induced a rNeu-specific anti-tumor immune response that prevented tumor formation of transplanted breast-tumor cells, and also protected mice from spontaneous tumor formation. Both T-cell-mediated and humoral immune responses were detectable in vaccinated mice. Vaccination also protected tumor-bearing mice from a challenge with cell suspensions isolated from spontaneous tumors, indicating that rNeu-TG mice are not tolerant to rNeu, even after spontaneous tumor formation. However, established spontaneous tumors themselves were never affected. This observation correlated with T-cell infiltrations in the injected but not in the established spontaneous tumor. Thus, allogeneic fibroblasts are efficient vaccine vectors to prime a specific immune response against an over-expressed tumor antigen. Moreover, our results suggest striking differences in the immunological requirements for the rejection of an established vs. a transplanted tumor.
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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 |
Oct
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pubmed:issn |
0020-7136
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 1999 Wiley-Liss, Inc.
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pubmed:issnType |
Print
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pubmed:day |
29
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pubmed:volume |
83
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
393-400
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:10495433-3T3 Cells,
pubmed-meshheading:10495433-Animals,
pubmed-meshheading:10495433-Antibodies, Neoplasm,
pubmed-meshheading:10495433-Antigens, CD3,
pubmed-meshheading:10495433-Female,
pubmed-meshheading:10495433-Graft Rejection,
pubmed-meshheading:10495433-Mammary Neoplasms, Animal,
pubmed-meshheading:10495433-Mice,
pubmed-meshheading:10495433-Mice, Inbred BALB C,
pubmed-meshheading:10495433-Mice, Transgenic,
pubmed-meshheading:10495433-Receptor, erbB-2,
pubmed-meshheading:10495433-T-Lymphocytes,
pubmed-meshheading:10495433-Vaccination
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pubmed:year |
1999
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pubmed:articleTitle |
Targeting HER-2/neu for active-specific immunotherapy in a mouse model of spontaneous breast cancer.
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pubmed:affiliation |
Department of Clinical Research, University of Bern, Bern, Switzerland.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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