Mason D Y, Leonard R C, Laurent G, Gourdin M F
J Clin Pathol. 1980 Jul;33(7):609-16. doi: 10.1136/jcp.33.7.609.
An immunoperoxidase technique for the optical microscopic detection of cellular immunoglobulin has been used to stain fixed smears of human neoplastic B lymphoid cells. Only four out of 28 cases of chronic lymphatic leukaemia (CLL) showed membrane labelling by this technique. In contrast, when 14 samples from other types of B lymphoproliferative disorder (including hairy cell leukaemia, non-Hodgkin's lymphoma, and prolymphocytic leukaemia) were studied, all samples showed membrane immunoglobulin labelling (confirmed by capping experiments). This discrepancy was attributed to the greater density of surface immunoglobulin present on neoplastic cells in the latter group of disorders compared to CLL. This immunoperoxidase technique is therefore less sensitive than immunofluorescent staining of cells in suspension for the demonstration of neoplastic cell surface immunoglobulin. However, it offers a number of advantages (eg, excellent visualisation of cell morphology, permanence of stained preparations, and applicability to stored samples) which recommend it as the method of choice in certain clinical haematological contexts.
一种用于光学显微镜检测细胞免疫球蛋白的免疫过氧化物酶技术已被用于对人肿瘤性B淋巴细胞固定涂片进行染色。在28例慢性淋巴细胞白血病(CLL)病例中,只有4例通过该技术显示出膜标记。相比之下,当研究来自其他类型B淋巴细胞增殖性疾病(包括毛细胞白血病、非霍奇金淋巴瘤和原淋巴细胞白血病)的14个样本时,所有样本均显示出膜免疫球蛋白标记(通过封帽实验证实)。这种差异归因于后一组疾病中的肿瘤细胞表面免疫球蛋白的密度高于CLL。因此,这种免疫过氧化物酶技术在显示肿瘤细胞表面免疫球蛋白方面不如对悬浮细胞进行免疫荧光染色敏感。然而,它具有许多优点(例如,细胞形态的良好可视化、染色制剂的永久性以及对储存样本的适用性),这些优点使其成为某些临床血液学情况下的首选方法。