Rehg J E, Hancock M L, Woodmansee D B
Comparative Medicine Division, St. Jude Children's Research Hospital, Memphis, Tennessee 38101.
Infect Immun. 1987 Nov;55(11):2669-74. doi: 10.1128/iai.55.11.2669-2674.1987.
A cyclophosphamide-treated-rat model for cryptosporidiosis is described. The optimal conditions for inducing a cryptosporidial infection in rats were a 50 mg/kg dose of cyclophosphamide per day in the drinking water for a minimum of 14 days before inoculation with 10(4) or more infectious oocysts. Eighteen days after inoculation, 80% or more of the animals were infected. Cryptosporidia were attached to the terminal 24 cm of the small intestine, and the immunosuppressed animals remained infected as long as they received cyclophosphamide. However, the intestinal infection cleared within 7 to 10 days after cyclophosphamide was withdrawn. Oocysts continued to be detected in the feces for an additional 5 to 7 days after cryptosporidia were no longer visibly attached to the ideal enterocytes. This study characterized an animal model that can be used to investigate the pathogenesis of and evaluate therapeutic regimens for cryptosporidiosis in the immunocompromised host.
描述了一种用于隐孢子虫病的环磷酰胺处理大鼠模型。在大鼠中诱导隐孢子虫感染的最佳条件是,在接种10(4)个或更多感染性卵囊前,在饮用水中每天给予50 mg/kg剂量的环磷酰胺,持续至少14天。接种后18天,80%或更多的动物被感染。隐孢子虫附着在小肠末端24 cm处,免疫抑制动物在接受环磷酰胺期间一直处于感染状态。然而,停用环磷酰胺后,肠道感染在7至10天内清除。在隐孢子虫不再明显附着于理想肠上皮细胞后,粪便中仍能检测到卵囊5至7天。本研究描述了一种动物模型,可用于研究免疫受损宿主中隐孢子虫病的发病机制并评估治疗方案。