Morris H B, Mason D Y, Stein H, Lennert K
Histopathology. 1983 Nov;7(6):809-23. doi: 10.1111/j.1365-2559.1983.tb02298.x.
The aim of this study was to document the patterns of cytoplasmic Ig heavy and light chain expression in reactive lymphoid tissue, using single and double immunoenzymatic labelling techniques. This investigation was undertaken, firstly, to provide information on whether the normal counterparts of high grade lymphoma cells (e.g. centroblasts, immunoblasts) ever express more than one light or heavy chain (as has been noted in the past for lymphomas) and also, secondly, to seek evidence of intraclonal 'switching' from cytoplasmic IgM to cytoplasmic IgG expression. Paraffin embedded sections, all showing substantial reactive changes, were analysed by means of immunoperoxidase stains for the three major immunoglobulin classes (IgG, IgM and IgA), both light chain classes and J chain. In addition, double immunoenzymatic labelling techniques were used to search for cells showing simultaneous expression of kappa and lambda light chains and cells expressing mu and gamma heavy chain. Large transformed lymphocytes showing cytoplasmic Ig-staining in the pulp and interfollicular areas often have nuclear morphology indistinguishable from germinal centre centroblasts. There was no evidence of primitive appearing IgM-positive cells and IgG-positive cells of more mature morphology. In addition, immunoenzymatic staining showed that cells simultaneously expressing both IgG and IgM are only rarely encountered. When such cells were detected, the morphology was not that of a blast cell, but rather of a plasma cell containing Russel bodies. Hence it is suggested that cytoplasmic IgM switching to IgG is rarely detected by immunohistological methods in reactive tissue. Double staining for kappa and lambda revealed that cells simultaneously expressing both light chain types were not detected even among cells showing the most primitive morphology.
本研究的目的是利用单免疫酶标和双免疫酶标技术,记录反应性淋巴组织中细胞质免疫球蛋白重链和轻链的表达模式。进行这项研究,首先是为了提供关于高级别淋巴瘤细胞的正常对应物(如中心母细胞、免疫母细胞)是否曾表达不止一种轻链或重链(如过去在淋巴瘤中所观察到的)的信息,其次是寻找克隆内从细胞质IgM向细胞质IgG表达“转换”的证据。对所有显示出明显反应性变化的石蜡包埋切片,采用免疫过氧化物酶染色法检测三种主要免疫球蛋白类别(IgG、IgM和IgA)、两种轻链类别以及J链。此外,使用双免疫酶标技术寻找同时表达κ和λ轻链的细胞以及表达μ和γ重链的细胞。在髓质和滤泡间区域显示细胞质Ig染色的大的转化淋巴细胞,其核形态通常与生发中心中心母细胞难以区分。没有证据表明存在形态幼稚的IgM阳性细胞和形态更成熟的IgG阳性细胞。此外,免疫酶标染色显示,同时表达IgG和IgM的细胞很少见。当检测到此类细胞时,其形态不是母细胞的形态,而是含有拉塞尔小体的浆细胞的形态。因此,提示在反应性组织中,通过免疫组织化学方法很少能检测到细胞质IgM向IgG的转换。κ和λ的双重染色显示,即使在形态最幼稚的细胞中,也未检测到同时表达两种轻链类型的细胞。