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免疫功能正常大鼠感染人隐孢子虫和微小隐孢子虫模型。

An immunocompetent rat model of infection with Cryptosporidium hominis and Cryptosporidium parvum.

机构信息

Department of Infectious Disease and Global Health, Cummings School of Veterinary Medicine, Tufts University, USA.

Department of Infectious Disease and Global Health, Cummings School of Veterinary Medicine, Tufts University, USA.

出版信息

Int J Parasitol. 2020 Jan;50(1):19-22. doi: 10.1016/j.ijpara.2019.10.002. Epub 2019 Nov 22.

Abstract

A major obstacle to developing vaccines against cryptosporidiosis, a serious diarrheal disease of children in developing countries, is the lack of rodent models essential to identify and screen protective immunogens. Rodent models commonly used for drug discovery are unsuitable for vaccine development because they either are purposefully immunodeficient or immunosuppressed. Here, we describe the development and optimization of an immunocompetent intratracheal (IT) rat model susceptible to infections with sporozoites of Cryptosporidium parvum and Cryptosporidium hominis - the primary causes of human cryptosporidiosis. A model suitable for screening of parasite immunogens is a prerequisite for immunogen screening and vaccine development.

摘要

开发针对隐孢子虫病(发展中国家儿童严重腹泻病)疫苗的主要障碍是缺乏识别和筛选保护性免疫原所必需的啮齿动物模型。用于药物发现的常用啮齿动物模型不适合疫苗开发,因为它们要么是故意免疫缺陷的,要么是免疫抑制的。在这里,我们描述了一种免疫功能健全的经气管(IT)大鼠模型的开发和优化,该模型易感染微小隐孢子虫和人隐孢子虫的孢子,这是人隐孢子虫病的主要原因。适合筛选寄生虫免疫原的模型是免疫原筛选和疫苗开发的前提。

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