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成年免疫功能正常和免疫抑制小鼠的微小隐孢子虫胆道感染

Cryptosporidium parvum biliary tract infection in adult immunocompetent and immunosuppressed mice.

作者信息

Verdon R, Polianski J, Grodet A, Garry L, Carbon C

机构信息

Service de Réanimation Médicale et Maladies Infectieuses, CHU Côte de Nacre, Caen, France.

出版信息

J Med Microbiol. 1998 Jan;47(1):71-7. doi: 10.1099/00222615-47-1-71.

Abstract

Biliary tract infection by Cryptosporidium parvum is a frequent complication of intestinal cryptosporidiosis in immunosuppressed patients. Although biliary tract infection can be produced in immunosuppressed models as a late complication of intestinal infection, there is no infection model in immunocompetent animals. A murine model of biliary tract cryptosporidiosis was developed by direct intra-gall bladder injection of C. parvum oocysts. In adult immunocompetent mice, intracellular parasitic stages were detected in the epithelium of the common bile duct in all animals on day 7 post-inoculation (p.i.). These findings were associated with a strong inflammatory reaction. Infection was cleared between days 14 and 21 p.i. All animals developed significant levels of specific serum and bile IgG, IgA and IgM. Dexamethasone treatment resulted in the inability of animals to eradicate the parasite and the establishment of ileal parasitism. This model can be used to study the immunological mechanisms involved in the control of biliary cryptosporidiosis.

摘要

隐孢子虫引起的胆道感染是免疫抑制患者肠道隐孢子虫病的常见并发症。尽管在免疫抑制模型中,胆道感染可作为肠道感染的晚期并发症出现,但在免疫功能正常的动物中尚无感染模型。通过直接向胆囊内注射微小隐孢子虫卵囊,建立了一种小鼠胆道隐孢子虫病模型。在成年免疫功能正常的小鼠中,接种后第7天,所有动物胆总管上皮细胞内均检测到细胞内寄生阶段。这些发现与强烈的炎症反应有关。感染在接种后第14天至21天清除。所有动物均产生了显著水平的特异性血清和胆汁IgG、IgA和IgM。地塞米松治疗导致动物无法清除寄生虫,并导致回肠寄生。该模型可用于研究控制胆道隐孢子虫病的免疫机制。

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