Source:http://linkedlifedata.com/resource/pubmed/id/10652572
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4B
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pubmed:dateCreated |
2000-2-15
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pubmed:abstractText |
Tumor associated lymphocytes (TAL) isolated from malignant ascites cultured in media containing interleukin-2 show antitumor responses. These antitumor responses are mediated by cytotoxic T lymphocytes (CTL) which recognize antigen in the context of MHC molecules using T cell receptors. CD8+ CTL recognize peptide epitopes processed from cellular proteins in the context of MHC class I molecules. These peptides have a restricted length of 8-11 amino acids. The folate binding protein (FBP) is overexpressed in over 90% of ovarian and 20-50% of breast cancers. We recently found that FBP is the source of antigenic peptides recognized by a number of these CTL-TAL. This indicated that FBP peptides are antigenic in vivo for ovarian and breast CTL-TAL. To define FBP immunogenicity, a peptide defining the epitope E39 (FBP, 191-199) was presented by PMBC derived dendritic cells (DC) from healthy donors isolated by the CD14 method to ovarian and breast CTL-TAL. Stimulation of ovarian and breast CTL-TAL by E39 pulsed DC (DC-E39), in the presence of IL-2, rapidly enhanced or induced E39 specific CTL activity. This E39-responder population consisted of cells expressing TCR V beta 9, V beta 13, and V beta 17 families, based on the increase in the percentages of these families in DC-E39 versus DC-NP stimulated TAL. Characterization of immunogenic tumor antigens and of cytokine requirements for induction of functional antitumor effectors may be important for future cancer vaccine developments.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Folate Receptors, GPI-Anchored,
http://linkedlifedata.com/resource/pubmed/chemical/Peptide Fragments,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Antigen, T-Cell...,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Cell Surface
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pubmed:status |
MEDLINE
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pubmed:issn |
0250-7005
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
19
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2907-16
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:10652572-Breast Neoplasms,
pubmed-meshheading:10652572-Carrier Proteins,
pubmed-meshheading:10652572-Cells, Cultured,
pubmed-meshheading:10652572-Female,
pubmed-meshheading:10652572-Folate Receptors, GPI-Anchored,
pubmed-meshheading:10652572-Humans,
pubmed-meshheading:10652572-Immunotherapy, Adoptive,
pubmed-meshheading:10652572-Lymphocyte Activation,
pubmed-meshheading:10652572-Lymphocytes, Tumor-Infiltrating,
pubmed-meshheading:10652572-Ovarian Neoplasms,
pubmed-meshheading:10652572-Peptide Fragments,
pubmed-meshheading:10652572-Receptors, Antigen, T-Cell, alpha-beta,
pubmed-meshheading:10652572-Receptors, Cell Surface,
pubmed-meshheading:10652572-T-Lymphocytes, Cytotoxic
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pubmed:articleTitle |
Folate binding protein peptide 191-199 presented on dendritic cells can stimulate CTL from ovarian and breast cancer patients.
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pubmed:affiliation |
Department of Gynecologic Oncology, University of Texas M.D. Anderson Cancer Center, Houston 77035, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
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