Ito M, Shichijo S, Miyagi Y, Kobayashi T, Tsuda N, Yamada A, Saito N, Itoh K
Department of Immunology, Kurume University School of Medicine, Kurume, Japan.
Int J Cancer. 2000 Nov 15;88(4):633-9. doi: 10.1002/1097-0215(20001115)88:4<633::aid-ijc18>3.0.co;2-n.
We recently identified the SART3 antigen encoding shared tumor epitopes recognized by HLA-A2402-restricted and tumor-specific CTLs. Our study investigated whether the SART3 antigen encodes peptides recognized by the HLA-A2-restricted CTLs. The HLA-A2-restricted and tumor-specific CTL line recognized COS-7 cells co-transfected with the SART3 gene and either HLA-A0201, -A0206 or -A0207 cDNA but not those co-transfected with the SART3 gene and HLA-A2402 or -A2601 cDNA. The 2 SART3 peptides at positions 302 to 310 and 309 to 317 possessed the ability to induce HLA-A2-restricted and tumor-specific CTLs from peripheral blood mononuclear cells of cancer patients with various histological types and different HLA-A2 subtypes. Therefore, these 2 peptides could be useful for specific immunotherapy of a relatively large number of HLA-A2(+) cancer patients.
我们最近鉴定出了SART3抗原,其编码被HLA - A2402限制性且肿瘤特异性的细胞毒性T淋巴细胞(CTL)识别的共享肿瘤表位。我们的研究调查了SART3抗原是否编码被HLA - A2限制性CTL识别的肽段。HLA - A2限制性且肿瘤特异性的CTL系识别与SART3基因以及HLA - A0201、-A0206或 -A0207 cDNA共转染的COS - 7细胞,但不识别与SART3基因以及HLA - A2402或 -A2601 cDNA共转染的COS - 7细胞。位于302至310位和309至317位的2个SART3肽段具有从患有各种组织学类型和不同HLA - A2亚型的癌症患者外周血单个核细胞诱导出HLA - A2限制性且肿瘤特异性CTL的能力。因此,这2个肽段可能对相当数量的HLA - A2(+)癌症患者的特异性免疫治疗有用。