Pileri S, Gerdes J, Rivano M, Tazzari P L, Magnani M, Gobbi M, Stein H
Br J Haematol. 1987 Mar;65(3):271-6. doi: 10.1111/j.1365-2141.1987.tb06853.x.
OKT9 and Ki-67 monoclonal antibodies have recently been proposed as useful tools for evaluating the growth fraction in malignant tumours, with special reference to non-Hodgkin's lymphomas. In particular, while the former is commonly thought to detect a transferrin receptor present on the cytoplasmic membrane of proliferating cells, the latter recognizes a nuclear antigen, which is expressed in G1, S, G2 and M phase of continuously cycling elements. To further verify their reliability, OKT9 and Ki-67 were applied to seven permanent cell lines (four myeloid and three B-lymphoblastoid) and 100 lymphoid tumours (70 non-Hodgkin's and 30 Hodgkin's lymphomas) phenotypically characterized on frozen sections. The results obtained showed that OKT9 and Ki-67 cannot be employed as equivalent means in assessing the growth fraction. In fact, OKT9 is directed to a transferrin receptor which is not only expressed by proliferating cells, but also by some resting elements. On the other hand, Ki-67 provides a nuclear, easily detectable positivity which is restricted to proliferating cells only. Therefore, it seems to represent the only monoclonal which can confidently be employed in the assessment of the growth fraction. Furthermore, the present study underlines that the immunocytochemical analysis of the proliferation rate in tumours gives similar information to the radionucleide uptake assay, while it represents a more sensitive method than the cytofluorimetric evaluation of the DNA content.
OKT9和Ki-67单克隆抗体最近被认为是评估恶性肿瘤生长分数的有用工具,特别是对于非霍奇金淋巴瘤。具体而言,前者通常被认为能检测增殖细胞细胞质膜上存在的转铁蛋白受体,而后者识别一种核抗原,该抗原在持续循环细胞的G1、S、G2和M期表达。为了进一步验证它们的可靠性,将OKT9和Ki-67应用于7种永久细胞系(4种髓系和3种B淋巴母细胞系)以及100例经冷冻切片表型特征化的淋巴样肿瘤(70例非霍奇金淋巴瘤和30例霍奇金淋巴瘤)。所获得的结果表明,OKT9和Ki-67在评估生长分数时不能作为等效手段。事实上,OKT9针对的是一种转铁蛋白受体,不仅增殖细胞表达该受体,一些静止细胞也表达。另一方面,Ki-67提供一种核内、易于检测的阳性,且仅局限于增殖细胞。因此,它似乎是唯一可自信地用于评估生长分数的单克隆抗体。此外,本研究强调,肿瘤增殖率的免疫细胞化学分析与放射性核素摄取测定提供相似的信息,同时它是一种比DNA含量的细胞荧光分析更敏感的方法。