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The Journal of Immunology, 1999, 163: 2783-2791.
Copyright © 1999 by The American Association of Immunologists

Identification of Natural Antigenic Peptides of a Human Gastric Signet Ring Cell Carcinoma Recognized by HLA-A31-Restricted Cytotoxic T Lymphocytes1

Kazuhiro Suzuki*,{dagger}, Hiroeki Sahara*,{ddagger}, Yohjiro Okada*,{dagger}, Takahiro Yasoshima{dagger}, Yoshihiko Hirohashi*, Yuki Nabeta*, Itaru Hirai*, Toshihiko Torigoe*, Shuji Takahashi*, Akihiro Matsuura*, Nobuaki Takahashi*,{ddagger}, Aya Sasaki*, Manabu Suzuki, Junji Hamuro, Hideyuki Ikeda||, Yoshimasa Wada{dagger}, Koichi Hirata{dagger}, Kokichi Kikuchi*,# and Noriyuki Sato2,*

Departments of * Pathology and {dagger} Surgery, Sapporo Medical University School of Medicine, Sapporo, Japan; {ddagger} Marine Biomedical Institute, Sapporo Medical University School of Medicine, Rishirifuji-cho, Hokkaido, Japan; § Department of Otolaryngology, Wakayama Medical College, Wakayama, Japan; Central Research Laboratories, Ajinomoto Co. Inc., Kawasaki, Japan; || Division of Cellular Signaling, Institute for Advanced Medical Research, Keio University School of Medicine, Tokyo, Japan; and # Sapporo Immunodiagnostic Laboratory, Sapporo, Japan

Peptides of human melanomas recognized by CD8+ CTLs have been identified, but the nature of those of nonmelanoma tumors remains to be elucidated. Previously, we established a gastric signet ring cell carcinoma HST-2 and HLA-A31 (A*31012)-restricted autologous CTL clone, TcHST-2. In the present study, we determined the natural antigenic peptides of HST-2 cells. The purified preparation of acid-extracted Ags was submitted to the peptide sequencer, and one peptide, designated F4.2 (Tyr-Ser-Trp-Met-Asp-Ile-Ser-Cys-Trp-Ile), appeared to be immunogenic. To confirm the antigenicity of F4.2 further, we constructed an expression minigene vector (pF4.2ss) coding adenovirus E3, a 19-kDa protein signal sequence plus F4.2. An introduction of pF4.2ss minigene to HST-2 and HLA-A31(+) allogeneic tumor cells clearly enhanced and induced the TcHST-2 reactivity, respectively. Furthermore, when synthetic peptides of F4.2 C-terminal-deleted peptides were pulsed to HST-2 cells, F4.2-9 (nonamers), but not F4.2-8 or F4.2-7 (octamer or heptamer, respectively), enhanced the reactivity of TcHST-2, suggesting that the N-terminal ninth Trp might be a T cell epitope. This was confirmed by lack of antigenicity when using synthetic substituted peptides as well as minigenes coding F4.2 variant peptides with Ala or Arg at the ninth position of F4.2. Meanwhile, it was indicated that the sixth position Ile was critically important for the binding to HLA-A31 molecules. Thus, our data indicate that F4.2 may work as an HLA-A31-restricted natural antigenic peptide recognized by CTLs.




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