Salter D M, Krajewski A S, Dewar A E
J Pathol. 1985 Aug;146(4):345-53. doi: 10.1002/path.1711460408.
Forty cases of non-Hodgkin's lymphoma (NHL) have been stained with monoclonal antibodies (F8-11-13, F-10-89-4 and Dako LC) to the Leucocyte Common Antigen (LC) in both cryostat and paraffin sections with an immunoperoxidase technique. In cryostat sections all B-cell lymphomas (25/25) reacted with F10-89-4 and Dako LC, whilst the majority (23/25) stained with F8-11-13; of the T-cell lymphomas studied, all reacted with F10-89-4 (6/60 and Dako LC (4/4), however 2/6 did not react with F8-11-13. Similar variability in reaction was observed in malignant histiocytosis where 1/3 did not react with F8-11-13 whilst all three reacted with F10-89-4 and Dako LC. In paraffin sections (using the two MCabs F8-11-13 and Dako LC) three of the 25 B-cell lymphomas failed to stain with either F8-11-13 or Dako LC (one lymphocytic lymphoma and two lymphomas showing plasmacytic differentiation). The remainder of the B-cell lymphomas reacted with both antibodies. Six out of 12 T-cell lymphomas did not stain with either F8-11-13 or Dako LC, using our standard immunoperoxidase procedure. Staining with Dako LC was however detected in all cases of T-cell lymphoma when incubation with primary antibody was extended from thirty minutes (standard) to overnight. This study confirmed that LC can be detected in all NHL in cryostat sections, and that in the majority of B-cell NHL the higher molecular weight component of LC was demonstrable using F8-11-13. Difficulty in detecting LC determinants after tissue processing for paraffin sections in a number of cases of NHL, especially those of T-cell type or showing plasmacytic differentiation, suggests that lack of reaction with these antibodies does not always preclude the diagnosis of lymphoma.
采用免疫过氧化物酶技术,运用针对白细胞共同抗原(LC)的单克隆抗体(F8 - 11 - 13、F - 10 - 89 - 4和Dako LC),对40例非霍奇金淋巴瘤(NHL)的冰冻切片和石蜡切片进行染色。在冰冻切片中,所有B细胞淋巴瘤(25/25)与F10 - 89 - 4和Dako LC发生反应,而大多数(23/25)被F8 - 11 - 13染色;在所研究的T细胞淋巴瘤中,所有病例均与F10 - 89 - 4(6/6)和Dako LC(4/4)发生反应,然而2/6不与F8 - 11 - 13反应。在恶性组织细胞增多症中也观察到类似的反应变异性,其中1/3不与F8 - 11 - 13反应,而所有三个病例均与F10 - 89 - 4和Dako LC反应。在石蜡切片中(使用两种单克隆抗体F8 - 11 - 13和Dako LC),25例B细胞淋巴瘤中有3例既不被F8 - 11 - 13也不被Dako LC染色(1例淋巴细胞淋巴瘤和2例显示浆细胞分化的淋巴瘤)。其余B细胞淋巴瘤与两种抗体均发生反应。按照我们的标准免疫过氧化物酶程序,12例T细胞淋巴瘤中有6例既不被F8 - 11 - 13也不被Dako LC染色。然而,当与一抗孵育时间从30分钟(标准时间)延长至过夜时,在所有T细胞淋巴瘤病例中均检测到Dako LC染色。本研究证实,在冰冻切片中可在所有NHL中检测到LC,并且在大多数B细胞NHL中,使用F8 - 11 - 13可显示LC的高分子量成分。在一些NHL病例中,尤其是T细胞型或显示浆细胞分化的病例,经石蜡切片组织处理后难以检测到LC决定簇,这表明与这些抗体缺乏反应并不总是排除淋巴瘤的诊断。