Soler P
INSERM U82, UFR Xavier Bichat, Paris.
Ann Pathol. 1995;15(1):75-9.
Immunohistochemical labeling of frozen tissue sections is a valuable technique that allows the detection of most antigens usually destroyed by fixation in conventional tissue processing. This technique, however, has a number of limitations: difficulty in storage of tissue samples, loss of morphologic details, presence of staining artifacts, diffusion of soluble proteins. The use of freeze-dried paraffin-embedded tissues is helpful in overcoming these problems: tissue morphology is better preserved than in frozen sections; a wide range of antigens can be labeled with the same staining intensity as in frozen sections; background or diffusion artifacts are uncommon; tissue blocks may be handled as conventional paraffin blocks. The technique is based on the rapid freezing of tissue samples and their subsequent freeze-drying, followed by embedding in paraffin. Because of the expense of the necessary equipment (tissue dryer) and the limited number of samples that can be processed at one time, this technique has not been widely used by routine pathological services.
冷冻组织切片的免疫组织化学标记是一项有价值的技术,它能够检测大多数在传统组织处理过程中因固定而被破坏的抗原。然而,该技术存在一些局限性:组织样本储存困难、形态细节丢失、存在染色假象、可溶性蛋白质扩散。使用冻干石蜡包埋组织有助于克服这些问题:组织形态比冷冻切片保存得更好;多种抗原可被标记,且染色强度与冷冻切片相同;背景或扩散假象不常见;组织块可像传统石蜡块一样处理。该技术基于组织样本的快速冷冻及其随后的冻干,然后进行石蜡包埋。由于所需设备(组织干燥器)成本高且一次能处理的样本数量有限,这项技术尚未被常规病理服务广泛应用。