Tiku M L, McNabb P C, Tomasi T B
Infect Immun. 1985 Sep;49(3):641-6. doi: 10.1128/iai.49.3.641-646.1985.
A model of disseminated histoplasmosis in CBA/J mice was developed. Cultures of Histoplasma capsulatum from the spleens of infected mice suggested almost complete clearance of fungi by week 3. The adherent spleen cells from infected mice showed a 2- to 20-fold increase in fibrinolysis. The increase in activity was maximal around 1 to 2 weeks and disappeared after week 3 of infection, and this paralleled the progressively decreasing number of culturable fungi from the spleen. In vitro coculture of infected spleen cells or nylon wool-purified immune T cells and proteose peptone-induced macrophages resulted in increased fibrinolysis. Peritoneal exudate cells from infected mice also showed increased fibrinolysis. The addition of soluble antigen to an in vitro culture system resulted not only in an increase in fibrinolytic activity of peritoneal exudate cells derived from infected mice but also of proteose peptone-induced macrophages. These observations suggest that spleen and peritoneal macrophages from H. capsulatum-infected mice exhibit increased fibrinolysis which in turn is indicative of macrophage activation. The mechanism of activation occurs as a result of immunologically specific T cell-macrophage interaction and by the action of histoplasma products on the macrophages. The significance of these findings and the role of the plasminogen activator assay in studies of disseminated fungal infection are discussed.
建立了CBA/J小鼠播散性组织胞浆菌病模型。从感染小鼠脾脏中培养荚膜组织胞浆菌,结果显示到第3周时真菌几乎完全清除。感染小鼠的贴壁脾细胞纤溶活性增加了2至20倍。活性增加在感染后1至2周左右达到最大值,感染第3周后消失,这与脾脏中可培养真菌数量的逐渐减少相一致。感染的脾细胞或经尼龙毛纯化的免疫T细胞与蛋白胨诱导的巨噬细胞进行体外共培养,导致纤溶活性增加。感染小鼠的腹腔渗出细胞也显示纤溶活性增加。向体外培养系统中添加可溶性抗原,不仅导致感染小鼠来源的腹腔渗出细胞纤溶活性增加,也使蛋白胨诱导的巨噬细胞纤溶活性增加。这些观察结果表明,荚膜组织胞浆菌感染小鼠的脾脏和腹腔巨噬细胞表现出纤溶活性增加,这反过来又表明巨噬细胞被激活。激活机制是免疫特异性T细胞 - 巨噬细胞相互作用以及组织胞浆菌产物对巨噬细胞作用的结果。讨论了这些发现的意义以及纤溶酶原激活物测定在播散性真菌感染研究中的作用。