呼吸道隐孢子虫病免疫抑制大鼠模型。

The Journal of protozoology Pub Date : 1991-11-01
J A Meulbroek, M N Novilla, W L Current
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引用次数: 0

摘要

描述了一种大鼠模型,其中动物发展为呼吸道隐孢子虫病,这种疾病在免疫功能低下的患者,特别是艾滋病患者中有很好的记录。我们目前对细小隐孢子虫呼吸道感染的病理生理学和免疫学知识的缺乏保证了实验动物模型的发展。皮下注射醋酸甲基强的松龙免疫抑制的Lewis大鼠,气管内接种10(6)个小孢子虫卵囊,在从气管到末端细支气管的气道上皮内发生了可复制的感染,包括所有已知的发育阶段。发育阶段在形态学上与肠上皮中所见的难以区分。接种后4天感染明显,接种后10-14天,大鼠表现出呼吸窘迫和严重体重减轻,肺扩大,有弹性。黏液分泌增加和上皮脱落性坏死导致大量黏液细胞渗出物在气道内积聚,并发斑片状肺泡炎,累及呼吸性细支气管的肺泡。
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An immunosuppressed rat model of respiratory cryptosporidiosis.

A rat model is described in which animals develop respiratory cryptosporidiosis, a disease which is well documented in immunocompromised patients, especially those with AIDS. Our present lack of knowledge of the pathophysiology and immunology of Cryptosporidium parvum respiratory infections warrants the development of a laboratory animal model. Lewis rats immunosuppressed by subcutaneous injection of methylprednisolone acetate and inoculated intratracheally with 10(6) C. parvum oocysts developed a reproducible infection consisting of all known developmental stages in the epithelium lining airways from the trachea to the terminal bronchioles. Developmental stages were morphologically indistinguishable from those seen in gut epithelium. Infections were apparent at 4 days post-inoculation, and at 10-14 days post-inoculation, rats exhibited respiratory distress and severe weight loss and had enlarged, elastic lungs. Increased mucus production and exfoliative necrosis of the epithelium resulted in accumulation of large amounts of mucocellular exudate throughout the airways and patchy alveolitis involving alveoli emerging from respiratory bronchioles.

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Proliferation patterns of latent Pneumocystis carinii in rat organs during progressive stages of immunosuppression. 7th European Conference on Cell and Molecular Biology of Ciliates. Toledo, Spain, September 2-6, 1991. Abstracts. The Society of Protozoologists. 1991 Abstracts. John O. Corliss--ciliatologist extraordinaire. Calcium transport and compartment analysis of free and exchangeable calcium in Plasmodium falciparum-infected red blood cells.
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