Barrios R, Santos G G, Figueroa J, Reyes P A
Am J Pathol. 1980 Jun;99(3):731-40.
An experimental model of hypersensitivity pneumonitis is presented. New Zealand white rabbits, previously immunized against yeast-derived zymosan, reacted to intratracheal challenge developing extensive pneumonitis. The lesions healed in a few weeks. Control animals challenged with inert particulate material (latex beads) or suspending fluid (PBS-Mg++) did not show pulmonary inflammation. Nonimmunized rabbits developed only transient pneumonitis after zymosan challenge. This reaction was clearly different from that seen in the group of immunized animals. The model reveals that biologically active substances such as zymosan, which is able to activate the alternate pathway of complement and mononuclear phagocytes, requires an active immune state in order to cause significant tissue damage. Isolated exposure to this kind of substance may not be sufficient to cause lung disease.
本文介绍了一种超敏性肺炎的实验模型。预先用酵母来源的酵母聚糖免疫的新西兰白兔,在气管内激发后出现广泛的肺炎。病变在几周内愈合。用惰性颗粒物质(乳胶珠)或悬浮液(PBS-Mg++)激发的对照动物未出现肺部炎症。未免疫的兔子在酵母聚糖激发后仅出现短暂的肺炎。这种反应与免疫动物组所见明显不同。该模型表明,能够激活补体替代途径和单核吞噬细胞的生物活性物质,如酵母聚糖,需要活跃的免疫状态才能造成显著的组织损伤。单独接触这种物质可能不足以导致肺部疾病。