Malinverni R, Kuo C C, Campbell L A, Grayston J T
Department of Pathobiology, University of Washington, Seattle 98195.
J Infect Dis. 1995 Aug;172(2):593-4. doi: 10.1093/infdis/172.2.593.
To study persistent infection, reactivation of Chlamydia pneumoniae lung infection in mice was attempted by immunosuppression with cortisone treatment. Four-week-old Swiss-Webster mice were treated with cortisone acetate (125 mg/kg) every other day for a total of six doses, starting on day 28 after intranasal inoculation of C. pneumoniae AR-39. C. pneumoniae was recovered from the lungs in 6 of 13 animals after six doses of cortisone, while control animals given saline remained negative. C. pneumoniae DNA was detected by polymerase chain reaction in the 6 culture-positive mice and 2 of 10 controls. The presence of pathogen DNA in this animal model suggested viable organisms in a culture-negative state.
为了研究持续性感染,尝试通过可的松治疗进行免疫抑制,以激活小鼠肺部肺炎衣原体感染的再激活。4周龄的瑞士韦伯斯特小鼠从鼻内接种肺炎衣原体AR-39后的第28天开始,每隔一天接受醋酸可的松(125 mg/kg)治疗,共六剂。在接受六剂可的松治疗后,13只动物中有6只从肺部分离出肺炎衣原体,而给予生理盐水的对照动物仍为阴性。通过聚合酶链反应在6只培养阳性小鼠和10只对照中的2只中检测到肺炎衣原体DNA。该动物模型中病原体DNA的存在表明在培养阴性状态下存在活的生物体。