| Literature DB >> 11823502 |
Maha Ayyoub1, Stefan Stevanovic, Ugur Sahin, Philippe Guillaume, Catherine Servis, Donata Rimoldi, Danila Valmori, Pedro Romero, Jean-Charles Cerottini, Hans-Georg Rammensee, Michael Pfreundschuh, Daniel Speiser, Frédéric Lévy.
Abstract
The tumor Ag SSX-2 (HOM-MEL-40) was found by serological identification of Ags by recombinant expression cloning and was shown to be a cancer/testis Ag expressed in a wide variety of tumors. It may therefore represent a source of CD8(+) T cell epitopes useful for specific immunotherapy of cancer. To identify potential SSX-2-derived epitopes that can be recognized by CD8(+) T cells, we used an approach that combined: 1) the in vitro proteasomal digestion of precursor peptides overlapping the complete SSX-2 sequence; 2) the prediction of SSX-2-derived peptides with an appropriate HLA-A2 binding score; and 3) the analysis of a tumor-infiltrated lymph node cell population from an HLA-A2(+) melanoma patient with detectable anti-SSX-2 serum Abs. This strategy allowed us to identify peptide SSX-2(41-49) as an HLA-A2-restricted epitope. SSX2(41-49)-specific CD8(+) T cells were readily detectable in the tumor-infiltrated lymph node population by multimer staining, and CTL clones isolated by multimer-guided cell sorting were able to lyse HLA-A2(+) tumor cells expressing SSX-2.Entities:
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Year: 2002 PMID: 11823502 DOI: 10.4049/jimmunol.168.4.1717
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422