Varki N M, Reisfeld R A, Walker L E
Cancer Res. 1984 Feb;44(2):681-7.
Monoclonal antibodies KS1/4, KS1/9, and KS1/17 were developed in this laboratory from a fusion of the murine myeloma cell line P3X63Ag8 with spleens of BALB/c mice previously primed with UCLA P3 cells derived from a human adenocarcinoma of the lung. Monoclonal antibodies KS1/4 and KS1/17 seemed to recognize similar glycoprotein antigens on the lung carcinoma cells by indirect immunoprecipitation and sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis. However, mapping of [3H]lysine- and [3H]arginine-labeled tryptic peptides of antigens in specific immunoprecipitates of lung carcinoma cells by high-pressure liquid chromatography revealed a one peptide difference. Antibody KS1/9 did not immunoprecipitate any identifiable protein from detergent extracts of the immunizing cell line by routine methods and appears to detect a glycolipid antigen. Immunocytochemical analysis of tissue sections showed this monoclonal antibody to be reactive with adenocarcinomas of the lung and not with the other histological types of lung carcinoma or normal tissue. Monoclonal antibodies KS1/4 and KS1/17, however, reacted with 3 major histological types of lung cancer and minimally with the proximal tubules of normal kidney and the epithelium of bronchioles.
单克隆抗体KS1/4、KS1/9和KS1/17是在本实验室由鼠骨髓瘤细胞系P3X63Ag8与先前用源自人肺腺癌的UCLA P3细胞免疫的BALB/c小鼠的脾脏融合而成。通过间接免疫沉淀和十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分析,单克隆抗体KS1/4和KS1/17似乎识别肺癌细胞上的相似糖蛋白抗原。然而,通过高压液相色谱对肺癌细胞特异性免疫沉淀物中抗原的[3H]赖氨酸和[3H]精氨酸标记的胰蛋白酶肽进行图谱分析,发现有一个肽段差异。抗体KS1/9通过常规方法不能从免疫细胞系的去污剂提取物中免疫沉淀任何可识别的蛋白质,似乎检测到一种糖脂抗原。组织切片的免疫细胞化学分析表明,这种单克隆抗体与肺腺癌反应,而不与其他组织学类型的肺癌或正常组织反应。然而,单克隆抗体KS1/4和KS1/17与3种主要组织学类型的肺癌反应,与正常肾近端小管和细支气管上皮的反应较弱。