Cellular immune responses against the cancer-testis antigen SPAN-XB in healthy donors and patients with multiple myeloma

The cancer-testis antigen SPAN-XB has been recently identified in multiple myeloma (MM). In the present study, we identified and characterized for the first time a cytotoxic cellular immune response against SPAN-XB in healthy donors and patients with MM. Using two independent computer algorithms, tw...

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Hauptverfasser: Frank, Christian (VerfasserIn) , Hundemer, Michael (VerfasserIn) , Ho, Anthony Dick (VerfasserIn) , Goldschmidt, Hartmut (VerfasserIn) , Witzens-Harig, Mathias (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 2008
In: Leukemia and lymphoma
Year: 2008, Jahrgang: 49, Heft: 4, Pages: 779-785
ISSN:1029-2403
DOI:10.1080/10428190801911688
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1080/10428190801911688
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Verfasserangaben:Christian Frank, Michael Hundemer, Anthony D. Ho, Hartmut Goldschmidt, Mathias Witzens-Harig

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520 |a The cancer-testis antigen SPAN-XB has been recently identified in multiple myeloma (MM). In the present study, we identified and characterized for the first time a cytotoxic cellular immune response against SPAN-XB in healthy donors and patients with MM. Using two independent computer algorithms, two SPAN-XB-derived peptides (peptides 624 and 626) with predicted binding to HLA-A2 were identified. To further improve the immunogenicity of peptide 626 we designed a heteroclitic peptide (peptide 627) by modifying one amino acid on the HLA binding position 2 of peptide 626. Using an IFN-γ Elispot assay we could demonstrate the presence and functional activity of CD8 peptide specific T cells with all tested peptides. By analysis of peripheral blood of 13 healthy donors and five patients with MM peptide specific T-cell precursors specifically recognizing at least one of the tested peptides could be detected and expanded in 9 of 13 of tested donors and 3 of 5 tested patients. Importantly, in two donors specific peptides could be generated against the heteroclitic peptide 627 but not against the native peptide 626. We conclude that SPAN-XB-derived peptides can elicit a consistent CD8 T cell response in healthy donors and patients with MM. 
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