Austin Health

Title
Cancer/testis antigens can be immunological targets in clonogenic CD133+ melanoma cells.
Publication Date
2009-02-17
Author(s)
Gedye, Craig
Quirk, Juliet
Browning, Judy
Svobodová, Suzanne
John, Thomas
Sluka, Pavel
Dunbar, P Rod
Corbeil, Denis
Cebon, Jonathan S
Davis, Ian D
Type of document
Journal Article
DOI
10.1007/s00262-009-0672-0
Abstract
"Cancer stem cells" that resist conventional treatments may be a cause of therapeutic failure in melanoma. We report a subpopulation of clonogenic melanoma cells that are characterized by high prominin-1/CD133 expression in melanoma and melanoma cell lines. These cells have enhanced clonogenicity and self-renewal in vitro, and serve as a limited in vitro model for melanoma stem cells. In some cases clonogenic CD133(+) melanoma cells show increased expression of some cancer/testis (CT) antigens. The expression of NY-ESO-1 in an HLA-A2 expressing cell line allowed CD133(+) clonogenic melanoma cells to be targeted for killing in vitro by NY-ESO-1-specific CD8(+) T-lymphocytes. Our in vitro findings raise the hypothesis that if melanoma stem cells express CT antigens in vivo that immune targeting of these antigens may be a viable clinical strategy for the adjuvant treatment of melanoma.
Link
Citation
Cancer Immunology, Immunotherapy : Cii 2009; 58(10): 1635-46
Jornal Title
Cancer immunology, immunotherapy : CII

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