Johnson K J, Ward P A
J Clin Invest. 1974 Aug;54(2):349-57. doi: 10.1172/JCI107770.
Acute immunologic injury of rat lung has been induced by the intrabronchial injection of heterologous antibody and the intravenous injection of radiolabeled antigen. Within 4 h an acute hemorrhagic neutrophil-rich exudate develops in alveolar and interstitial areas and then gradually fades. Lung injury in this model can be quantitated by measurements of increased vascular permeability and extractable hemoglobin. By the use of immunofluorescent techniques, alveolar and interstitial deposits of antigen and antibody have been demonstrated, but not the third component of complement (C3). Although not found in relation to immune complexes, C3 is nevertheless present in damaged lung as measured by accumulation of radiolabeled C3 from the circulation. Ablation experiments indicate the requirement for both circulating neutrophils and C3 for the development of lung injury. These studies provide definition for the development of lung damage induced by immune complexes.
通过支气管内注射异源抗体和静脉注射放射性标记抗原,已诱导大鼠肺发生急性免疫损伤。在4小时内,肺泡和间质区域会出现富含中性粒细胞的急性出血性渗出物,然后逐渐消退。该模型中的肺损伤可通过测量血管通透性增加和可提取血红蛋白来定量。通过免疫荧光技术,已证实抗原和抗体在肺泡和间质中沉积,但未发现补体第三成分(C3)。虽然未发现C3与免疫复合物有关,但通过循环中放射性标记C3的积累测量发现,受损肺中存在C3。切除实验表明,肺损伤的发生需要循环中的中性粒细胞和C3。这些研究为免疫复合物诱导的肺损伤的发展提供了定义。