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治疗隐孢子虫病的化疗方法综述。

A review of chemotherapeutic approaches to the treatment of cryptosporidiosis.

作者信息

Armson Anthony, Thompson R C Andrew, Reynoldson James A

机构信息

Western Australian Biomedical Research Institute, Division of Health Sciences, Murdoch University, Perth. Western Australia.

出版信息

Expert Rev Anti Infect Ther. 2003 Aug;1(2):297-305. doi: 10.1586/14787210.1.2.297.

Abstract

This review focuses on chemotherapies used against the parasite, Cryptosporidium parvum, the causative agent of cryptosporidiosis. Populations at risk from severe morbidity or mortality from cryptosporidiosis are discussed with particular reference to those infected with HIV. The review then examines chemotherapies used in the clinical setting, as well as a number of in vitro and in vivo experimental studies. It begins with a discussion of the targets within Cryptosporidium that have been the foci of past treatments and then examines novel target sites that may present an exploitable alternative. Some of the novel target sites discussed include the recently discovered apicomplexan plastid and its associated pathways. Lastly, the review examines tubulin as a potential anticryptosporidial target in view of the fact that it has been exploited successfully for almost 50 years for the treatment of helminthiasis. The review concludes with a five-year outlook on the future of anticryptosporidial drug design.

摘要

本综述聚焦于用于对抗微小隐孢子虫(隐孢子虫病的病原体)的化疗方法。文中讨论了有患严重隐孢子虫病发病或死亡风险的人群,特别提及了感染艾滋病毒的人群。该综述接着审视了临床环境中使用的化疗方法,以及一些体外和体内实验研究。开篇讨论了过去治疗中作为重点的隐孢子虫内部靶点,然后研究了可能提供可利用替代方案的新靶点。所讨论的一些新靶点包括最近发现的顶复门质体及其相关途径。最后,鉴于微管蛋白在治疗蠕虫病方面已成功应用近50年,该综述将其作为潜在的抗隐孢子虫靶点进行了研究。综述最后对抗隐孢子虫药物设计的未来进行了五年展望。

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