rdf:type |
|
lifeskim:mentions |
umls-concept:C0025202,
umls-concept:C0030705,
umls-concept:C0039194,
umls-concept:C0085358,
umls-concept:C0108789,
umls-concept:C0175630,
umls-concept:C0441655,
umls-concept:C1332717,
umls-concept:C1413191,
umls-concept:C1413244,
umls-concept:C1515021,
umls-concept:C1706438,
umls-concept:C2348480,
umls-concept:C2698600,
umls-concept:C2700400
|
pubmed:issue |
6
|
pubmed:dateCreated |
2002-3-25
|
pubmed:abstractText |
To defend the host from malignancies, the immune system can spontaneously raise CD8(+) T-cell responses against tumor antigens. Investigating the functional state of tumor-reactive cytolytic T cells in cancer patients is a key step for understanding the role of these cells in tumor immunosurveillance and for evaluating the potential of immunotherapeutic approaches of vaccination against cancer. In this study we identified a subset of circulating tumor-reactive CD8(+) T lymphocytes, which specifically secreted IFN-gamma after exposition to autologous tumor cell lines in stage IV metastatic melanoma patients. Additional phenotypic characterization using multicolor flow cytometry revealed that a significant fraction of these cells were CD45RA(+)CCR7(-), a phenotype that has been proposed recently to characterize cytolytic effectors potentially able to home into inflamed tissues. In the case of an HLA-A2-expressing patient, the antigen specificity of this population was identified by using HLA-A2/peptide multimers incorporating a tyrosinase-derived peptide. Consistently with their phenotypic characteristics, A2/tyrosinase peptide multimer(+) CD8(+) T cells, isolated by cell sorting, were directly lytic ex vivo and able to specifically recognize tyrosinase-expressing tumor cells. Overall, these results provide the first evidence that a proportion of melanoma patients have circulating tumor-reactive T cells, which are lytic effectors cells.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD45,
http://linkedlifedata.com/resource/pubmed/chemical/CCR7 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Epitopes, T-Lymphocyte,
http://linkedlifedata.com/resource/pubmed/chemical/HLA-A2 Antigen,
http://linkedlifedata.com/resource/pubmed/chemical/Monophenol Monooxygenase,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, CCR7,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Chemokine
|
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
0008-5472
|
pubmed:author |
pubmed-author:AsemissenAnne MarieAM,
pubmed-author:CerottiniJean-CharlesJC,
pubmed-author:DietrichPierre-YvesPY,
pubmed-author:DutoitValerieV,
pubmed-author:GuillaumePhilippeP,
pubmed-author:KeilholzUlrichU,
pubmed-author:LiénardDanielleD,
pubmed-author:LippMartinM,
pubmed-author:NagorsenDirkD,
pubmed-author:RimoldiDonataD,
pubmed-author:RomeroPedroP,
pubmed-author:Rubio-GodoyVerenaV,
pubmed-author:SchadendorfDirkD,
pubmed-author:ScheibenbogenCarmenC,
pubmed-author:ThielEckhardE,
pubmed-author:ValmoriDanilaD
|
pubmed:issnType |
Print
|
pubmed:day |
15
|
pubmed:volume |
62
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1743-50
|
pubmed:dateRevised |
2007-11-15
|
pubmed:meshHeading |
pubmed-meshheading:11912149-Antigens, CD45,
pubmed-meshheading:11912149-CD8-Positive T-Lymphocytes,
pubmed-meshheading:11912149-Cytotoxicity, Immunologic,
pubmed-meshheading:11912149-Epitopes, T-Lymphocyte,
pubmed-meshheading:11912149-HLA-A2 Antigen,
pubmed-meshheading:11912149-Humans,
pubmed-meshheading:11912149-Lymphocyte Activation,
pubmed-meshheading:11912149-Melanoma,
pubmed-meshheading:11912149-Monophenol Monooxygenase,
pubmed-meshheading:11912149-Receptors, CCR7,
pubmed-meshheading:11912149-Receptors, Chemokine,
pubmed-meshheading:11912149-T-Lymphocyte Subsets,
pubmed-meshheading:11912149-T-Lymphocytes, Regulatory
|
pubmed:year |
2002
|
pubmed:articleTitle |
Circulating Tumor-reactive CD8(+) T cells in melanoma patients contain a CD45RA(+)CCR7(-) effector subset exerting ex vivo tumor-specific cytolytic activity.
|
pubmed:affiliation |
Division of Clinical Onco-Immunology, Ludwig Institute for Cancer Research, University Hospital, 1005 Lausanne, Switzerland.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|