An improved rat model of Pneumocystis carinii pneumonia: induced infections in Pneumocystis-free animals.

The Journal of protozoology Pub Date : 1991-11-01
C J Boylan, W L Current
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引用次数: 0

Abstract

An immunosuppressed rat model of Pneumocystis carinii pneumonia (PCP) is described that results in a predictable course of disease development which includes moderate P. carinii (Pc) infections in 2 to 3 weeks, heavy infections in 4 to 5 wk, and a high percentage of mortality due to PCP in 6 wk. The model also provides uninfected, immunosuppressed contemporary controls, an experimental compartment that is needed to correctly interpret results obtained from many different studies. Non-invasive intratracheal inoculation of cryopreserved parasites into Pc- and virus-free rats immunosuppressed by weekly injections of methylprednisolone are key features of the model that result in the development of consistent heavy Pc infections and very few secondary infections by bacteria and fungi. This model is useful for (1) maintaining isolates or strains of Pc over time, (2) producing large numbers of parasites for laboratory studies, and (3) evaluating the anti-Pc activity of experimental compounds and approved drugs.

改良的卡氏肺囊虫肺炎大鼠模型:无肺囊虫动物诱导感染。
本文描述了一种免疫抑制的卡氏肺囊虫肺炎(PCP)大鼠模型,其结果是可预测的疾病发展过程,包括2至3周的中度卡氏肺囊虫(Pc)感染,4至5周的重度感染,以及6周内卡氏肺囊虫肺炎的高死亡率。该模型还提供了未感染的、免疫抑制的当代对照,这是正确解释从许多不同研究中获得的结果所需要的实验隔间。通过每周一次注射甲基强的松龙,将冷冻保存的寄生虫无创气管内接种到无Pc和无病毒的大鼠中,这是该模型的关键特征,导致持续的重度Pc感染和很少由细菌和真菌引起的继发感染。该模型可用于(1)长期维持Pc的分离株或菌株,(2)产生用于实验室研究的大量寄生虫,以及(3)评估实验化合物和批准药物的抗Pc活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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