Pennington J E
J Infect Dis. 1977 Jul;136(1):127-31. doi: 10.1093/infdis/136.1.127.
The use of immunosuppressive chemotherapy is associated with an increased incidence of pneumonia. An animal model is described in which drug-induced defects in pulmonary host defense may be evaluated. Guinea pigs receiving cyclophosphamide (15 mg/kg) plus cortisone acetate (100 mg/kg) daily for seven days developed leukopenia (1.5 X 10(3) cells/mm3), neutropenia (0.4 X 10(3)/mm3), and lymphocytopenia (0.7 X 10(3)/mm3) and also lost prior skin hypersensitivity to purified protein derivative. No animal bled or died unexpectedly during immunosuppression. Transtracheal bronchoalveolar lavage of normal and immunosuppressed animals revealed a significant decrease in the number of pulmonary alveolar macrophages during immunosuppressed periods. Cell viability, phagocytosis of latex particlex, and adherence to plastic surfaces were not decreased in immunosuppressed alveolar macrophages. This animal model should allow further studies of cellular and humoral pulmonary immune parameters during a variety of immunosuppressive drug regimens.
免疫抑制化疗的使用与肺炎发病率增加有关。本文描述了一种动物模型,可用于评估药物诱导的肺部宿主防御缺陷。豚鼠连续七天每天接受环磷酰胺(15毫克/千克)加醋酸可的松(100毫克/千克),出现白细胞减少(1.5×10³个细胞/立方毫米)、中性粒细胞减少(0.4×10³/立方毫米)和淋巴细胞减少(0.7×10³/立方毫米),并且对纯化蛋白衍生物的皮肤超敏反应也消失。在免疫抑制期间,没有动物意外出血或死亡。对正常和免疫抑制动物进行经气管支气管肺泡灌洗发现,在免疫抑制期间肺泡巨噬细胞数量显著减少。免疫抑制的肺泡巨噬细胞的细胞活力、乳胶颗粒吞噬作用和对塑料表面的黏附性并未降低。该动物模型应有助于在各种免疫抑制药物方案期间进一步研究细胞和体液肺部免疫参数。