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Detection of nonspecific immunohistochemical response caused by tissue necrosis and the presence of metallic wear debris

机译:检测组织坏死引起的非特异性免疫组织化学反应及金属磨损碎片的存在

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Tissues retrieved during revision arthroplasty (n=25) were processed for routine immunohistochemical techniques to localize the presence of bone resorbing cytokines (IL-1 and IL-6), and to identify areas of significant necrosis and metallic deposition. Tissues were processed and embedded according to standard laboratory techniques. Several slides were prepared for each tissue sample taken. Several sequential slides were stained for Hematoxylin and Eosin to demonstrate cell type. Other slides of the same tissues were processed for localization of cytokines, IL-1 and IL-6. To identify specific cytokine reactions, the tissues were first blocked with proteins to ensure that all. The results revealed that there were several locations on the tissues that appeared highly reactive for cytokines IL-1 and IL-6. However, some of these areas turned out to be nonspecific when compared with negative controls and the Hematoxylin and Eosin stained slides. Areas of extreme necrosis or where metal debris was presence demonstrated sites of nonspecific reactivity. Areas of necrosis have a high nonspecific affinity for antibodies and these areas of necrosis can be demonstrated on the Hematoxylin and Eosin sections, and should be avoided in determining the amount of specific cellular reactivity. In addition, new immunohistochemical techniques use cobalt ions as enhancers of peroxidase response, in areas on slides labeled as negative controls where metallic debris was trapped, there was an increase in nonspecific positive reactivity. These factors must be carefully controlled in determining true cellular responses that causes resorption of bone and implant failure.
机译:在修正关节成形术期间检索的组织被加工用于常规免疫组织化学技术以定位骨再现细胞因子(IL-1和IL-6)的存在,并鉴定显着坏死和金属沉积的区域。根据标准实验室技术处理和嵌入组织。为每种组织样品制备几种载玻片。用于苏木精和曙红染色几个序贯载玻片以演示细胞类型。处理相同组织的其他载玻片以用于细胞因子,IL-1和IL-6的定位。为了鉴定特异性细胞因子反应,首先用蛋白质封闭组织以确保所有。结果表明,在细胞因子IL-1和IL-6出现高反应性的组织上存在几个位置。然而,与阴性对照和血毒素和曙红染色的载玻片相比,这些区域中的一些是非特异性。极端坏死的区域或金属碎片的存在展示了非特异性反应性的位点。坏死区域对抗体具有高的非特异性亲和力,并且可以在血液杂志和曙红切片上证明这些坏死区域,并且应该在确定特定细胞反应性的量时避免。此外,新的免疫组织化学技术使用钴离子作为过氧化物酶反应的增强剂,在标记为阴性对照的载玻片的区域中,非特异性阳性反应性增加。必须仔细控制这些因素在确定导致骨骼和植入失败的真正的细胞反应中。

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