Hiraiwa N, Iida N, Ishizuka I, Itai S, Shigeta K, Kannagi R, Fukuda Y, Imura H
Department of Clinical Science and Laboratory Medicine, Kyoto University, School of Medicine, Japan.
Cancer Res. 1988 Dec 1;48(23):6769-74.
Two murine monoclonal antibodies, 2H6G5 (IgM) and 4A9E10 (IgG3), were obtained by using either cultured human hepatocellular carcinoma cells (PLC/PRF/5) or the acidic glycolipid mixture prepared from the same cells as immunogens. The antigen in PLC/PRF/5 cell membranes recognized by both antibodies was identified as a disulfated acidic glycolipid, GgOse4Cer-II3IV3-bis-sulfate (SB1a). Both antibodies reacted specifically with SB1a, and no significant reactivity was noted with other sulfated glycolipids or gangliosides except that the antibody 2H6G5 showed a weak cross-reactivity with LacCer-II3-sulfate (SM3), another sulfated glycolipid which partly shares the same carbohydrate structure as SB1a. The SB1a antigen is a relatively minor glycolipid in PLC/PRF/5 cells, but it was strongly expressed at the surface of PLC/PRF/5 cells as ascertained by cytofluorometry using both antibodies. A significant amount of SB1a antigen was present in 3 of the acidic glycolipid fractions isolated from 15 human hepatocellular carcinoma tissues as well as in the acidic glycolipid fraction prepared from PLC/PRF/5 cells, while all the acidic glycolipid fractions prepared from cirrhotic livers and a normal liver were essentially negative for SB1a, as ascertained by both solid phase enzyme immunoassay and the thin-layer chromatography-immunostaining method. These results strongly suggest that the SB1a antigen as defined by these new monoclonal antibodies is associated with human hepatocellular carcinoma.
通过使用培养的人肝癌细胞(PLC/PRF/5)或由相同细胞制备的酸性糖脂混合物作为免疫原,获得了两种鼠单克隆抗体,2H6G5(IgM)和4A9E10(IgG3)。两种抗体识别的PLC/PRF/5细胞膜中的抗原被鉴定为二硫酸化酸性糖脂,GgOse4Cer-II3IV3-双硫酸盐(SB1a)。两种抗体均与SB1a特异性反应,除抗体2H6G5与硫酸乳糖神经酰胺-II3-硫酸盐(SM3)有弱交叉反应外,未观察到与其他硫酸化糖脂或神经节苷脂有明显反应,SM3是另一种硫酸化糖脂,其部分碳水化合物结构与SB1a相同。SB1a抗原在PLC/PRF/5细胞中是一种相对较少的糖脂,但通过使用两种抗体的细胞荧光测定法确定,它在PLC/PRF/5细胞表面强烈表达。从15个人肝癌组织分离的3种酸性糖脂组分以及从PLC/PRF/5细胞制备的酸性糖脂组分中存在大量SB1a抗原,而通过固相酶免疫测定和薄层色谱-免疫染色法确定,从肝硬化肝脏和正常肝脏制备的所有酸性糖脂组分对SB1a基本呈阴性。这些结果强烈表明,由这些新的单克隆抗体定义的SB1a抗原与人肝癌相关。