Merz H, Rickers O, Schrimel S, Orscheschek K, Feller A C
Institute of Pathology, Medical University of Lübeck, Germany.
J Pathol. 1993 Jul;170(3):257-64. doi: 10.1002/path.1711700307.
The introduction of microwave detection systems has significantly enhanced the sensitivity of immunohistochemistry in formalin-fixed, paraffin-embedded tissue. The combination of protease digestion and microwave treatment including the use of heavy metal salts or urea gives an Ig heavy and light chain detection system in formalin-fixed and paraffin-embedded material as good as that achieved using fresh frozen material, with the advantage of a well-preserved morphology. The sensitivity of this method depends on the heavy metal salt used and its concentration. The use of urea yields equally sensitive results, while avoiding the toxicity of heavy metal salts. Heating times in the microwave oven also have an important influence on the results. The microwave-based technique may allow for the improved accessibility of formalin-masked antigens, as was shown here for cytoplasmic and surface immunoglobulins. It was demonstrated that formalin-fixed specimens of Burkitt's lymphoma when subjected to the new protocol almost always showed surface Ig expression, giving results comparable to those obtained in frozen sections. Moreover, it could be shown that in cases of B-chronic lymphocytic lymphoma (B-CLL) or immunocytoma, surface and cytoplasmic Ig could be detected, so that the difference may be just a quantitative one and thus may no longer be safely used as a criterion in differential diagnosis. In future, the wide use of this technique will allow for the study of Ig expression at the single cell level in morphologically well-preserved material.
微波检测系统的引入显著提高了福尔马林固定、石蜡包埋组织中免疫组织化学的灵敏度。蛋白酶消化与微波处理相结合,包括使用重金属盐或尿素,在福尔马林固定、石蜡包埋材料中可得到与新鲜冷冻材料一样好的Ig重链和轻链检测系统,且具有形态保存良好的优点。该方法的灵敏度取决于所用重金属盐及其浓度。使用尿素可产生同样灵敏的结果,同时避免了重金属盐的毒性。微波炉中的加热时间对结果也有重要影响。基于微波的技术可能使福尔马林掩盖的抗原更容易被检测到,如本文中对细胞质和表面免疫球蛋白的检测所示。结果表明,伯基特淋巴瘤的福尔马林固定标本采用新方案处理后几乎总能显示表面Ig表达,其结果与冷冻切片相当。此外,可以证明在B细胞慢性淋巴细胞白血病(B-CLL)或免疫细胞瘤病例中,可以检测到表面和细胞质Ig,因此差异可能只是数量上的,从而可能不再安全地用作鉴别诊断的标准。未来,这项技术的广泛应用将有助于在形态保存良好的材料中研究单细胞水平的Ig表达。