Proteasome-assisted identification of a SSX-2-derived epitope recognized by tumor-reactive CTL infiltrating metastatic melanoma

M Ayyoub, S Stevanovic, U Sahin… - The Journal of …, 2002 - journals.aai.org
M Ayyoub, S Stevanovic, U Sahin, P Guillaume, C Servis, D Rimoldi, D Valmori, P Romero…
The Journal of Immunology, 2002journals.aai.org
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) …
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.
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