Cattoretti G, Becker M H, Key G, Duchrow M, Schlüter C, Galle J, Gerdes J
Istituto Nazionale per lo Studio e la Cura dei Tumori, Department of Pathology, Milano, Italy.
J Pathol. 1992 Dec;168(4):357-63. doi: 10.1002/path.1711680404.
The monoclonal antibody Ki-67 reacts with a human nuclear cell proliferation-associated antigen that is expressed in all active parts of the cell cycle. Recently we have raised monoclonal antibodies, MIB 1-3, against recombinant parts of the Ki-67 antigen. These antibodies are true Ki-67 equivalents, as demonstrated by immunostaining of fresh specimens, biochemistry, and molecular biological techniques. Formalin-fixed, paraffin-embedded sections routinely processed for immunohistochemistry failed to stain for Ki-67 and MIB 2. Antibodies MIB 1 and MIB 3 labelled mitotic figures, while non-mitotic proliferating cells were negative under these conditions. However, when dewaxed microwave oven-processed paraffin sections of formalin-fixed tissues were used, MIB 1 and MIB 3 gave strong nuclear staining of those cells presumed to proliferate under a variety of normal and neoplastic conditions. Moreover, routine decalcification or depigmentation techniques did not alter the immunoreactivity of MIB 1 and MIB 3 with microwave-processed paraffin sections. This method is highly reproducible, easy to perform at low cost, and no additional technical skill is needed because after microwave treatment just routine immunohistochemical methods are used. Since we have successfully applied this new method to sections obtained from paraffin blocks stored for a long time (in one case more than 60 years), the assessment of cell kinetics through the detection of Ki-67 antigen is now possible on archival material collected in histopathology departments all over the world.
单克隆抗体Ki-67可与人核细胞增殖相关抗原发生反应,该抗原在细胞周期的所有活跃阶段均有表达。最近,我们制备了针对Ki-67抗原重组部分的单克隆抗体MIB 1 - 3。通过新鲜标本免疫染色、生物化学和分子生物学技术证明,这些抗体是真正的Ki-67等效物。常规处理用于免疫组织化学的福尔马林固定、石蜡包埋切片未能对Ki-67和MIB 2进行染色。在这些条件下,抗体MIB 1和MIB 3标记有丝分裂图像,而非有丝分裂增殖细胞呈阴性。然而,当使用福尔马林固定组织经微波炉处理脱蜡的石蜡切片时,MIB 1和MIB 3对那些在各种正常和肿瘤条件下推测为增殖的细胞产生强烈的核染色。此外,常规脱钙或脱色技术不会改变MIB 1和MIB 3对经微波处理的石蜡切片的免疫反应性。该方法具有高度可重复性,易于低成本实施,且不需要额外的技术技能,因为微波处理后只需使用常规免疫组织化学方法。由于我们已成功将这种新方法应用于从长期保存(一例超过60年)的石蜡块中获得的切片,现在通过检测Ki-67抗原对细胞动力学进行评估在世界各地组织病理学部门收集的存档材料上成为可能。