Pertot W J, Sindres V, Szekeres G, Proust J P
Universite de la Mediterranee, Faculte d'Odontologie, Secteur Nord, Marseille, France.
J Biomed Mater Res. 1997 Mar 15;34(4):457-62. doi: 10.1002/(sici)1097-4636(19970315)34:4<457::aid-jbm6>3.0.co;2-j.
The purpose of this study was to propose a new method for quantitative evaluation of the pulpal inflammation to restorative materials using immunohistochemistry and image analysis. Class V cavities were prepared and filled with different restorative materials in 20 healthy premolars to be extracted for orthodontic reasons. Teeth were extracted at different time intervals, fixed, demineralized, and embedded in paraffin. Six-micrometer-thick sections were cut serially and mounted on slides and every fifth section was stained using hematoxylin and eosin or Masson's trichrome, and served to localize the inflammatory reaction. The slides corresponding to the bulk of the inflammatory reaction were then used for immunohistochemical detection of the inflammatory cells using monoclonal antibodies: CD15 (granulocytes and histiocytes), CD45RO (T lymphocytes and monocytes), Pan-B cell (B lymphocytes, macrophages, and a subpopulation of T lymphocytes), CD45RA (B lymphocytes and monocytes), and EMA (plasma cells). The slides were observed and submitted to computerized image analysis using a SAMBA 2000 system for counting of the cells. The CD15, CD45RO, Pan-B-cell, and CD45RA antibodies positively stained the target cells, which could be counted with the computer. The EMA antibody did not permit staining of cells. These results indicate that polymorphonuclears, T lymphocytes, and B lymphocytes are present in inflamed human dental pulp. The immunologic detection of inflammatory cells followed by computerized image analysis allows an accurate characterization of pulpal pathology, and could be useful for the study of pulp reactions to restorative biomaterials.
本研究的目的是提出一种使用免疫组织化学和图像分析对牙髓对修复材料的炎症进行定量评估的新方法。制备20颗因正畸原因需拔除的健康前磨牙的Ⅴ类洞,并使用不同的修复材料进行充填。在不同时间间隔拔牙,固定、脱矿并石蜡包埋。连续切取6微米厚的切片并载于载玻片上,每隔五张切片用苏木精和伊红或Masson三色染色,用于定位炎症反应。然后将与炎症反应主体相对应的载玻片用于使用单克隆抗体对炎症细胞进行免疫组织化学检测:CD15(粒细胞和组织细胞)、CD45RO(T淋巴细胞和单核细胞)、泛B细胞(B淋巴细胞、巨噬细胞和T淋巴细胞亚群)、CD45RA(B淋巴细胞和单核细胞)和EMA(浆细胞)。观察载玻片并使用SAMBA 2000系统进行计算机图像分析以计数细胞。CD15、CD45RO、泛B细胞和CD45RA抗体对靶细胞进行阳性染色,这些细胞可用计算机计数。EMA抗体不能使细胞染色。这些结果表明多形核细胞、T淋巴细胞和B淋巴细胞存在于发炎的人牙髓中。炎症细胞的免疫检测随后进行计算机图像分析可准确表征牙髓病理学,并且可用于研究牙髓对修复生物材料的反应。