Warnke R
J Histochem Cytochem. 1979 Aug;27(8):1195-6. doi: 10.1177/27.8.113452.
Four large cell lymphomas known to be monoclonal B-cell proliferations were studied with immunofluorescent and immunohistochemical methods for the detection of kappa- and lambda-light chains. Frozen sections of lymphoma tissues as well as formalin and B-5-fixed tissues embedded in paraffin were studied. Both immunofluorescent and immunohistochemical methods gave similar results on frozen sections; however, a number of discrepancies were noted between the results obtained on fixed tissues and those obtained on frozen tissues. In an effort to identify a fixative which did not alter immunoglobulin (Ig), mouse lymph nodes were fixed in different fixatives before Ig detection; but all of the fixatives tested destroyed the Ig present on normal cortical B lymphocytes. Immunoglobulin-bearing normal and neoplastic lymphocytes are better detected on frozen sections than on paraffin sections after routine fixation.
采用免疫荧光和免疫组化方法对4例已知为单克隆B细胞增殖的大细胞淋巴瘤进行κ和λ轻链检测。研究了淋巴瘤组织的冰冻切片以及用福尔马林和B-5固定并包埋于石蜡中的组织。免疫荧光和免疫组化方法在冰冻切片上得到了相似的结果;然而,在固定组织上获得的结果与在冰冻组织上获得的结果之间存在一些差异。为了确定一种不改变免疫球蛋白(Ig)的固定剂,在检测Ig之前,将小鼠淋巴结用不同的固定剂固定;但所有测试的固定剂都破坏了正常皮质B淋巴细胞上存在的Ig。与常规固定后的石蜡切片相比,冰冻切片能更好地检测出携带免疫球蛋白的正常和肿瘤淋巴细胞。