Guggenheim B, Schroeder H E
Infect Immun. 1974 Sep;10(3):565-77. doi: 10.1128/iai.10.3.565-577.1974.
The purpose of our experiment was to evaluate the destructive potential of a strain of Actinomyces viscosus on the periodontium of sensitized rodents, describing the induced lesions on the basis of quantitative cytology. The experimental design comprised in principle the following procedures. Young germfree rats were immunized either by intravenous or intradermal injections with heat-killed cells of A. viscosus Ny 1 or sham immunized intradermally with physiological saline. After a period suitable for activation of the humoral and cell-mediated immune systems, Ny 1 was monoassociated in all animals by oral implantation. During the ensuing 42 days the animals were allowed to react against the continuous peripheral oral antigen challenge. Since A. viscosus is known as a heavy dental plaque-forming organism, the animals could be expected to develop local immunopathological lesions in the periodontal tissues. These lesions were then studied by quantitative cytology after sampling procedures allowing optimal tissue preservation. The degree of bone loss observed in all treatments was unrelated to the destructive capacity of the infiltrates, suggesting the presence of distinct mechanisms responsible for the activation of osteoclasts and factors interfering with fibroblast activity. Although the cellular composition of the infiltrated tissues was analyzed at the end of the experiment only, distinct stages of the lesions in the different treatments allowed reconstruction of the sequence of events. After an acute inflammatory phase, a classic delayed hypersensitivity reaction developed which was transformed after some time by a large superimposed plasma cell accumulation. The particular but undefined immune status was the significant factor determining the final type of peripheral infiltrative reaction.
我们实验的目的是评估一株粘性放线菌对致敏啮齿动物牙周组织的破坏潜力,并基于定量细胞学描述所诱发的病变。实验设计原则上包括以下步骤。将年轻的无菌大鼠通过静脉注射或皮内注射用热灭活的粘性放线菌Ny 1细胞进行免疫,或用生理盐水进行假皮内免疫。在适合激活体液免疫和细胞介导免疫的时间段后,通过口腔植入使所有动物单一关联Ny 1。在随后的42天里,让动物对持续的外周口腔抗原刺激做出反应。由于粘性放线菌是一种形成大量牙菌斑的微生物,可以预期动物会在牙周组织中发生局部免疫病理损伤。然后在采用能实现最佳组织保存的采样程序后,通过定量细胞学研究这些损伤。在所有处理中观察到的骨吸收程度与浸润物的破坏能力无关,这表明存在导致破骨细胞激活的不同机制以及干扰成纤维细胞活性的因素。尽管仅在实验结束时分析了浸润组织的细胞组成,但不同处理中损伤的不同阶段使得能够重建事件序列。在急性期炎症之后,出现了典型的迟发型超敏反应,一段时间后因大量叠加的浆细胞积聚而转变。特定但未明确的免疫状态是决定外周浸润性反应最终类型的重要因素。