Study of HLA class I restriction and the directed antigens of cytotoxic T lymphocytes at the tumor sites of ovarian cancer

被引:0
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作者
Akira Yamada
Koichiro Kawano
Nanae Harashima
Fumihiko Niiya
Kouji Nagai
Terutada Kobayashi
Takashi Mine
Kimio Ushijima
Takashi Nishida
Kyogo Itoh
机构
[1] Cancer Vaccine Development Division,
[2] Kurume University Research Center for Innovative Cancer Therapy,undefined
[3] and Department of Immunology,undefined
[4] Kurume University School of Medicine,undefined
[5] Asahi-machi 67,undefined
[6] Kurume,undefined
[7] Fukuoka 830-0011,undefined
[8] Japan e-mail: akiymd@med.kurume-u.ac.jp,undefined
[9] Fax: +81-942-31-7745,undefined
[10] Cancer Vaccine Development Division,undefined
[11] Kurume University Research Center for Innovative Cancer Therapy,undefined
[12] Kurume 830,undefined
[13] Japan,undefined
[14] Department of Obstetrics and Gynecology,undefined
[15] Kurume University School of Medicine,undefined
[16] Kurume 830,undefined
[17] Japan,undefined
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关键词
Key words Cytotoxic T lymphocytes; Ovarian cancer; Tumor antigen; HLA restriction;
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摘要
The molecular basis of T-cell-mediated recognition of ovarian cancer cells remains to be fully addressed. In this study we investigated HLA class I restriction and directed antigens of cytotoxic T lymphocytes (CTL) at the sites of ovarian cancer. Three HLA-class-I-restricted CTL lines were established from the tumor sites of ovarian cancer by culturing tumor-infiltrating lymphocytes or tumor-associated ascitic lymphocytes with interleukin-2: (1) HLA-A2402-restricted and ovarian-adenocarcinoma-specific CTL, (2) HLA-A2-restricted CTL recognizing histologically different cancers, and (3) HLA-B52-restricted and ovarian-cancer-specific CTL. HLA-A0201, HLA-A0206 and HLA-A0207 tumor cells were lysed by the HLA-A2-restricted CTL. HLA-B52 restriction of the third CTL line was confirmed by the transfection of HLA-B5201 cDNA into the tumor cells. The HLA-A2-restricted CTL recognized the SART-1, but not the MAGE-1 or MAGE-3 antigen. These results may facilitate a better understanding of the molecular basis of tumor-specific immunity at the tumor site of ovarian cancer.
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页码:147 / 152
页数:5
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