Maeda Kunihiko, Matsuda Mikio, Suzuki Hitoshi, Saitoh Hito-Aki
Department of Pathology, Yamagata University School of Medicine, Yamagata, Japan.
J Histochem Cytochem. 2002 Nov;50(11):1475-86. doi: 10.1177/002215540205001107.
A number of monoclonal antibodies (MAbs) that recognize human follicular dendritic cells (FDCs) have been identified. Although some of them have already been applied individually in routine immunolabeling using formalin-fixed paraffin sections for diagnostic and experimental purposes, many antibodies are still employed only for immunolabeling using cryostat sections or particularly processed sections because they have been thought unsuitable for routine sections. A comprehensive examination re-evaluating their suitability in paraffin sections has not been reported. Accordingly, there is limited ability to examine the immunopathological contribution or diagnostic value of FDCs using routinely processed specimens or archived materials. In this study a broad panel of antibodies was systematically applied to the immunolabeling of paraffin sections of reactive tonsils or lymph nodes, in combination with advanced antigen retrieval (AR) techniques. Several antibodies, including Ki-M4p, X-11, 12B1, CNA.42, 1F8/BU32 (anti-CD21), BU38/1B12 (anti-CD23), Ber-MAC-DRC/To5 (anti-CD35), 1.4C3 (anti-CD106), NGFR5 (anti-nerve growth factor receptor p75), IIH6 (anti-CD55), 55K-2 (anti-fascin), and anti-S100 protein alpha-chain, were found to label FDCs in routine sections when combined with suitable AR techniques. Our results are easily adaptable for routine practice and provided useful suggestions concerning the immunopathological behavior and diversity of the particular cells.
已经鉴定出多种识别人类滤泡树突状细胞(FDC)的单克隆抗体(MAb)。尽管其中一些已单独应用于使用福尔马林固定石蜡切片的常规免疫标记,用于诊断和实验目的,但许多抗体仍仅用于使用冷冻切片或经过特殊处理的切片进行免疫标记,因为它们被认为不适用于常规切片。尚未有关于重新评估它们在石蜡切片中适用性的全面研究报告。因此,使用常规处理的标本或存档材料来研究FDC的免疫病理学作用或诊断价值的能力有限。在本研究中,将一组广泛的抗体与先进的抗原修复(AR)技术相结合,系统地应用于反应性扁桃体或淋巴结石蜡切片的免疫标记。发现几种抗体,包括Ki-M4p、X-11、12B1、CNA.42、1F8/BU32(抗CD21)、BU38/1B12(抗CD23)、Ber-MAC-DRC/To5(抗CD35)、1.4C3(抗CD106)、NGFR5(抗神经生长因子受体p75)、IIH6(抗CD55)、55K-2(抗肌动蛋白)和抗S100蛋白α链,与合适的AR技术结合时可在常规切片中标记FDC。我们的结果易于应用于常规实践,并为特定细胞的免疫病理学行为和多样性提供了有用的建议。