Khavkin T, Tabibzadeh S S
Interferon Sciences, Inc., New Brunswick, New Jersey 08901.
Infect Immun. 1988 Jul;56(7):1792-9. doi: 10.1128/iai.56.7.1792-1799.1988.
A histologic, immunofluorescence, and electron microscopic study of the intracellular parasitism of Coxiella burnetii (the Q fever agent) in mouse lungs after intranasal challenge was undertaken. It was shown that this microorganism invades type I and, rarely, type II pneumocytes as well as pulmonary fibroblasts and histiocytes. The infectious process can be described as a focal intra-alveolar inflammation with the macrophages prevailing in the exudate. It is self-limited, with a complete resolution. The inflammation is associated with atelectases and with increased secretory activity by type II pneumocytes. Alveolar macrophages and granulocytes degrade C. burnetii. This degradation is followed by damage to and eventual disintegration of some macrophages and by damage to some bacterium-free pneumocytes and vascular endothelial cells in the vicinity of macrophages degrading organisms. The cell damage might be caused by lipopolysaccharide released from degraded organisms. The infectious process is also associated with the influx of T cells in the pneumonic foci, T-cell attachment to the macrophages degrading organisms, and fusion of some macrophages. These are considered a morphologic expression of cell-mediated immunity involved in the infectious process.
对经鼻攻击后小鼠肺部伯氏考克斯体(Q热病原体)细胞内寄生情况进行了组织学、免疫荧光及电子显微镜研究。结果表明,这种微生物可侵入I型肺细胞,极少情况下也可侵入II型肺细胞,以及肺成纤维细胞和组织细胞。感染过程可描述为肺泡内局灶性炎症,渗出物中以巨噬细胞为主。该过程具有自限性,可完全消退。炎症与肺不张以及II型肺细胞分泌活性增加有关。肺泡巨噬细胞和粒细胞可降解伯氏考克斯体。这种降解之后,一些巨噬细胞会受损并最终解体,同时在降解病原体的巨噬细胞附近,一些无细菌的肺细胞和血管内皮细胞也会受损。细胞损伤可能是由降解病原体释放的脂多糖引起的。感染过程还与肺炎病灶中T细胞的流入、T细胞与降解病原体的巨噬细胞的附着以及一些巨噬细胞的融合有关。这些被认为是感染过程中细胞介导免疫的形态学表现。