Ryning F W, Remington J S
Infect Immun. 1977 Dec;18(3):746-53. doi: 10.1128/iai.18.3.746-753.1977.
As pulmonary involvement can occur in disseminated toxoplasmosis in immunosuppressed patients, studies were initiated to define local mechanisms of resistance of the lung to Toxoplasma gondii. Alveolar macrophages were obtained from normal mice and mice chronically infected with T. gondii by bronchopulmonary lavage and cultured in vitro. Although normal alveolar macrophages were difficult to infect with Toxoplasma, they supported intracellular multiplication of this organism. When exposed to Toxoplasma that had been pretreated with heat-inactivated serum containing specific antibody, the number of intracellular organisms increased remarkably, and the macrophages destroyed the coated parasites. After development of chronic infections with Toxoplasma, there was a transient period during which a striking increase in numbers of alveolar macrophages was observed in lavage specimens. These macrophages differed from those of normal alveolar macrophages. There was a greater percentage of large cells, a greater tendency to spread on glass, and an increased number of intracellular Toxoplasma, and the cells were activated to kill or inhibit multiplication of the parasite. During the period when activated macrophages were demonstrable in bronchopulmonary washings, histological changes in the lungs revealed a marked mononuclear cell infiltrate. These studies support a role for the activated alveolar macrophage as an effector in resistance of the lung to infection with Toxoplasma.
由于免疫抑制患者的播散性弓形虫病可累及肺部,因此开展了相关研究以明确肺部对刚地弓形虫的局部抵抗机制。通过支气管肺灌洗从正常小鼠和慢性感染弓形虫的小鼠获取肺泡巨噬细胞,并在体外进行培养。虽然正常肺泡巨噬细胞很难被弓形虫感染,但它们支持该病原体在细胞内增殖。当暴露于用含有特异性抗体的热灭活血清预处理过的弓形虫时,细胞内病原体数量显著增加,且巨噬细胞会破坏被包裹的寄生虫。在弓形虫慢性感染形成后,在灌洗标本中观察到肺泡巨噬细胞数量有一个短暂的显著增加期。这些巨噬细胞与正常肺泡巨噬细胞不同。大细胞的比例更高,在玻璃上铺展的倾向更大,细胞内弓形虫数量增加,且细胞被激活以杀死或抑制寄生虫的增殖。在支气管肺灌洗中可检测到活化巨噬细胞的时期,肺部的组织学变化显示有明显的单核细胞浸润。这些研究支持活化肺泡巨噬细胞在肺部抵抗弓形虫感染中作为效应细胞发挥作用。