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昏睡病的分子诊断:对患者有何益处?

Molecular diagnostics for sleeping sickness: what is the benefit for the patient?

机构信息

Department of Parasitology, Institute of Tropical Medicine, Antwerp, Belgium.

出版信息

Lancet Infect Dis. 2010 Jun;10(6):433-9. doi: 10.1016/S1473-3099(10)70077-3.

Abstract

Sleeping sickness, or human African trypanosomiasis, is a vector-borne disease caused by two subspecies of the protozoan parasite Trypanosoma brucei, and is geographically restricted to sub-Saharan Africa. Although the disease causes major public-health and socioeconomic problems among affected populations, sleeping sickness is one of the world's most neglected diseases. Within the rapidly evolving field of biotechnology, many molecular diagnostics have been developed to detect the parasite. These range from conventional, high-tech, and low-tech PCR formats (eg, isothermal nucleic-acid-amplification techniques), to direct visualisation of the parasite's nucleic acids by fluorescent probes. Besides reviewing the most important molecular diagnostics available, we discuss their current role in diagnosis and disease control. Although powerful, molecular diagnostics are confined to research settings and do not reach the patient or national control programmes. The current formats are not applicable to field conditions, and simplification, standardisation, and proper test evaluation in the target setting should be the main focus for future development.

摘要

昏睡病,又称非洲人类锥虫病,是一种由原生动物寄生虫布氏锥虫的两个亚种引起的虫媒病,仅在撒哈拉以南非洲流行。尽管该病给受影响人群带来了重大的公共卫生和社会经济问题,但昏睡病仍是世界上被忽视程度最高的疾病之一。在快速发展的生物技术领域,已经开发出许多分子诊断方法来检测寄生虫。这些方法包括传统的、高科技的和低技术的 PCR 格式(例如,等温核酸扩增技术),以及通过荧光探针直接观察寄生虫的核酸。除了回顾现有的最重要的分子诊断方法外,我们还讨论了它们在诊断和疾病控制中的当前作用。尽管分子诊断方法非常强大,但它们仅限于研究环境,无法到达患者或国家控制计划。目前的方法不适用于野外条件,简化、标准化和在目标环境中进行适当的测试评估应是未来发展的主要重点。

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