TY - JOUR
T1 - Identification of an HLA-A24-restricted OY-TES-1 epitope recognized by cytotoxic T-cells
AU - Okumura, Hideo
AU - Noguchi, Yuji
AU - Uenaka, Akiko
AU - Aji, Toshiki
AU - Ono, Toshiro
AU - Nakagawa, Kazuhiko
AU - Aoe, Motoi
AU - Shimizu, Nobuyoshi
AU - Nakayama, Eiichi
PY - 2005
Y1 - 2005
N2 - OY-TES-1 was identified as a human homologue of the mouse, guinea pig, and pig proacrosin binding protein sp32 precursor. Differential expression levels of OY-TES-1 mRNA between testis and other normal tissues, and its expression in cancers indicated that OY-TES-1 would be classified as a cancer/testis antigen and considered to be a candidate of target antigen for cancer immunotherapy. In this study, we showed identification of HLA-A24-binding OY-TES-1 peptide, TES401-409, (KTPFVSPLL) recognized by CD8 T-cells. Purified CD8 T-cells from healthy donors stimulated in vitro with the peptide-pulsed autologous DC and PBMC produced IFNγ in response to the peptide-pulsed PBMC and showed cytotoxicity against the peptide-pulsed autologous EBV-B specifically. Furthermore, cytotoxicity was also observed against an OY-TES-1 mRNA-expressing tumor line, LK79. The retention time of the fraction in HPLC of the acid eluate from LK79 cells that showed positive sensitization against autologous EBV-B cells in recognition by CD8 CTL was the same as that of the fraction of the TES401-409 peptide itself, suggesting that the TES401-409 was a naturally processed peptide on LK79.
AB - OY-TES-1 was identified as a human homologue of the mouse, guinea pig, and pig proacrosin binding protein sp32 precursor. Differential expression levels of OY-TES-1 mRNA between testis and other normal tissues, and its expression in cancers indicated that OY-TES-1 would be classified as a cancer/testis antigen and considered to be a candidate of target antigen for cancer immunotherapy. In this study, we showed identification of HLA-A24-binding OY-TES-1 peptide, TES401-409, (KTPFVSPLL) recognized by CD8 T-cells. Purified CD8 T-cells from healthy donors stimulated in vitro with the peptide-pulsed autologous DC and PBMC produced IFNγ in response to the peptide-pulsed PBMC and showed cytotoxicity against the peptide-pulsed autologous EBV-B specifically. Furthermore, cytotoxicity was also observed against an OY-TES-1 mRNA-expressing tumor line, LK79. The retention time of the fraction in HPLC of the acid eluate from LK79 cells that showed positive sensitization against autologous EBV-B cells in recognition by CD8 CTL was the same as that of the fraction of the TES401-409 peptide itself, suggesting that the TES401-409 was a naturally processed peptide on LK79.
KW - Acid extraction
KW - CTL epitope
KW - Cancer/testis antigen
KW - OY-TES-1
UR - http://www.scopus.com/inward/record.url?scp=28044440694&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=28044440694&partnerID=8YFLogxK
U2 - 10.1111/j.1348-0421.2005.tb03688.x
DO - 10.1111/j.1348-0421.2005.tb03688.x
M3 - Article
C2 - 16301813
AN - SCOPUS:28044440694
SN - 0385-5600
VL - 49
SP - 1009
EP - 1016
JO - MICROBIOLOGY and IMMUNOLOGY
JF - MICROBIOLOGY and IMMUNOLOGY
IS - 11
ER -