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Immunochemical and Immunohistological Analyses of Tumor‐associated Antigens Defined by Murine Monoclonal Antibodies against Human Pancreatic Carcinoma Cells

机译:针对人类胰腺癌细胞的鼠单克隆抗体定义的肿瘤相关抗原的免疫化学和免疫组织学分析。

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摘要

Two murine monoclonal antibodies, SK‐930 (isotype IgG2a) and SK‐117 (isotype IgG1), were produced from spleen cells of mice immunized against human pancreatic carcinoma cell lines, MIA‐PaCa 2 and Panc‐1. With the use of the avidin‐biotin‐immunoperoxidase technique, the SK‐930 and SK‐117 antibodies detected an antigen found in 24 and 23 formalin‐fixed tissue sections, respectively, of tumors obtained from 30 different patients with pancreatic carcinoma. Reactivity was also frequently found with tumors of the gallbladder, bile duct, stomach, colon and esophagus, while a large panel of normal human tissues, including normal pancreatic tissues, displayed little reactivity. These observations suggest that SK‐930 and SK‐117 are of value in identifying tumor‐associated antigen (TAA) expressed in pancreatic carcinoma and other carcinomas of the digestive system. SK‐930 antibody immunoprecipitated a 134 kilodalton molecule from extracts of 125I‐ or [35S]methionine‐ or [3H]glucosamine‐labeled tumor cells. The SK‐117‐defined antigen corresponds to 152/137 kilodalton molecules. Moreover, cytofluorometric analyses showed that cells treated with periodic acid exhibited greatly decreased reactivity to the two antibodies, but cells treated with neuraminidase, trypsin or pronase showed unchanged reactivity. The findings suggest that the epitopes of the novel TAA expressed on pancreatic carcinoma cells are carbohydrate moieties.
机译:从针对人胰腺癌细胞系MIA-PaCa 2和Panc-1免疫的小鼠的脾细胞中产生了两种鼠类单克隆抗体SK-930(同种IgG2a)和SK-117(同种IgG1)。通过使用抗生物素蛋白-生物素-免疫过氧化物酶技术,SK-930和SK-117抗体分别在30例不同的胰腺癌患者的肿瘤中分别在24个和23个福尔马林固定的组织切片中检测到一种抗原。在胆囊,胆管,胃,结肠和食道肿瘤中也经常发现反应性,而一大堆正常人组织,包括正常胰腺组织,则几乎没有反应性。这些观察结果表明,SK-930和SK-117在鉴定胰腺癌和其他消化系统癌中表达的肿瘤相关抗原(TAA)方面具有重要价值。 SK‐930抗体从 125 I-或[ 35 S]蛋氨酸或[ 3 H]葡糖胺提取物中免疫沉淀一个134道尔顿分子标记的肿瘤细胞。 SK‐117定义的抗原对应于152/137千道尔顿分子。此外,细胞荧光分析表明,用高碘酸处理的细胞对两种抗体的反应性大大降低,但是用神经氨酸酶,胰蛋白酶或链霉蛋白酶处理的细胞则未发生反应。这些发现表明在胰腺癌细胞上表达的新型TAA的表位是碳水化合物部分。

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