Sakamoto J, Kojima H, Kato J, Hamashima H, Suzuki H
Department of Surgery, Aichi Prefectural Hospital, Kakemachi, Okazaki, Japan.
Cancer Chemother Pharmacol. 2000;46 Suppl:S27-32. doi: 10.1007/pl00014045.
Murine monoclonal antibody A33 (mA33) was developed by the Memorial Sloan-Kettering Cancer Center and by the New York Branch of the Ludwig Institute for Cancer Research. It is an immunoglobulin (Ig)G2a antibody that detects a protease- and neuraminidase-resistant, periodate-sensitive epitope. Serological analysis of the antigen showed that it is expressed in a few colorectal cancer cell lines and a pancreatic cancer cell line, but is basically not reactive with other types of cell line. Normal fibroblasts and normal kidney cell lines reacted negatively to mA33. Immunohistochemical study of normal tissues identified the large and small intestinal mucosa as the principal site of A33 expression. Tests in tumor samples demonstrated that only tumors of the gastrointestinal tract are consistently A33 positive. A33 is found in 95% of primary and metastatic colorectal cancers, with uniform expression throughout the tumors in most cases. A33 is also detected in 63% of gastric cancers, with uniform expression in 45% of cases. Eighty-three percent of intestinal-type gastric cancers were positive for A33, and about 50% of the diffuse-type and mucinous cancers were mA33 positive. A33 was expressed in 50% of the pancreatic cancers but with marked heterogeneity. Other epithelial cancers, sarcomas, neuroectodermal tumors, and lymphoid neoplasms were generally A33 negative. A33 is the first example of a constitutively expressed, organ-specific epithelial membrane antigen permitting highly specific tumor targeting in patients with gastrointestinal cancer. Encouraged by the success of the biodistribution and imaging characteristic studies performed at Memorial Sloan-Kettering Cancer Center by the New York Branch of the Ludwig Institute in colorectal cancers, a new clinical study of humanized monoclonal antibody huA33 against A33 antigen-positive gastric cancers has been initiated in Japan.
鼠单克隆抗体A33(mA33)由纪念斯隆凯特琳癌症中心和路德维希癌症研究所纽约分所研制。它是一种免疫球蛋白(Ig)G2a抗体,可检测一种对蛋白酶和神经氨酸酶有抗性、对高碘酸盐敏感的表位。对抗原的血清学分析表明,它在少数结肠癌细胞系和一个胰腺癌细胞系中表达,但基本上与其他类型的细胞系无反应。正常成纤维细胞和正常肾细胞系对mA33呈阴性反应。对正常组织的免疫组织化学研究确定大肠和小肠黏膜是A33表达的主要部位。肿瘤样本检测表明,只有胃肠道肿瘤始终呈A33阳性。95%的原发性和转移性结肠直肠癌中可发现A33,大多数情况下肿瘤中表达一致。63%的胃癌中也检测到A33,45%的病例中表达一致。83%的肠型胃癌A33呈阳性,约50%的弥漫型和黏液癌mA33呈阳性。50%的胰腺癌中表达A33,但具有明显的异质性。其他上皮癌、肉瘤、神经外胚层肿瘤和淋巴瘤通常A33呈阴性。A33是组成性表达的器官特异性上皮膜抗原的首个实例,可使胃肠道癌患者实现高度特异性的肿瘤靶向。受路德维希癌症研究所纽约分所在纪念斯隆凯特琳癌症中心对结肠直肠癌进行的生物分布和成像特征研究取得成功的鼓舞,日本已启动一项针对A33抗原阳性胃癌的人源化单克隆抗体huA33的新临床研究。