Capurro M, Bover L, Portela P, Livingston P, Mordoh J
Instituto de Investigaciones Bioquímicas Fundación Campomar, Buenos Aires, Argentina.
Cancer Immunol Immunother. 1998 Feb;45(6):334-9. doi: 10.1007/s002620050451.
FC-2.15 is a murine IgM monoclonal antibody that recognizes breast and colon human carcinomas, chronic myeloid leukemias, Sternberg cells of Hodgkin's lymphoma and some normal cells, such as peripheral polymorphonuclear granulocytes. It has been previously demonstrated that FC-2.15 recognizes the carbohydrate moiety of different glycoproteins. FC-2.15 is able to mediate the in vitro lysis of Ag-2.15+ cells by human complement. In a phase I clinical trial, FC-2.15 induced antitumor responses and reversible neutropenia was its main toxicity. In this work, analysis of epitope specificity has demonstrated that FC-2.15 specifically recognizes terminally exposed Lewis(x) trisaccharide but not sialyl-Lewis(x), Lewis(a), trifucosylated Lewis(y), blood-group antigens A and B, globo H and gangliosides. In polymorphonuclear granulocytes (PMN), myeloid leukemic cells and colon carcinoma T84 cells, Lewis(x) was found to be almost exclusively N-linked to the protein core, whereas in breast carcinoma MCF-7 cells, Lewis(x) appeared to be mostly O-linked. Treatment with neuraminidase increased detection by FC-2.15 in normal PMN, myeloid leukemia cells and T84 cells but not in MCF-7 cells.
FC - 2.15是一种鼠源IgM单克隆抗体,可识别乳腺和结肠人类癌组织、慢性粒细胞白血病、霍奇金淋巴瘤的斯腾伯格细胞以及一些正常细胞,如外周多形核粒细胞。先前已证明FC - 2.15可识别不同糖蛋白的碳水化合物部分。FC - 2.15能够介导人补体对Ag - 2.15 +细胞的体外裂解作用。在一项I期临床试验中,FC - 2.15诱导了抗肿瘤反应,其主要毒性为可逆性中性粒细胞减少。在这项研究中,表位特异性分析表明,FC - 2.15特异性识别末端暴露的Lewis(x)三糖,而不识别唾液酸化Lewis(x)、Lewis(a)、三岩藻糖基化Lewis(y)、血型抗原A和B、球H和神经节苷脂。在多形核粒细胞(PMN)、髓系白血病细胞和结肠癌T84细胞中,发现Lewis(x)几乎完全与蛋白核心N连接,而在乳腺癌MCF - 7细胞中,Lewis(x)似乎大多为O连接。用神经氨酸酶处理可增加FC - 2.15在正常PMN、髓系白血病细胞和T84细胞中的检测,但在MCF - 7细胞中则不然。