血吸虫病相关循环无细胞DNA:诊断中有用的生物标志物

IF 1.4 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Hanif Ullah , Safia Arbab , Ka Li , Muhammad Inayat Ullah Khan , Abdul Qadeer , Nehaz Muhammad
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引用次数: 4

摘要

血吸虫是一种引起血吸虫病的吸虫属,是一种被忽视的主要热带病,在世界热带和亚热带地区,特别是低收入国家,有2.4亿多人感染,7亿人面临感染风险。为了消除这种疾病,需要准确的诊断工具。除了允许早期治疗外,早期发现还可以防止环境污染,从而确保流行地区的安全水源。无细胞DNA (cfDNA)生物标志物检测是一种相对较新的工具,用于从非侵入性临床或实验样本中诊断血吸虫病感染的早期阶段。cfDNA可在血吸虫感染宿主的尿液、血清、唾液和组织等体液中检测到,主要存在于血液中,为准确诊断提供了显著的好处。在当前的综述中,我们描述了cfDNA的不同特征,证据和支持其在血吸虫病诊断和提高治疗效果方面的潜在应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Schistosomiasis related circulating cell-free DNA: A useful biomarker in diagnostics

Schistosoma is a genus of trematodes causing schistosomiasis, a major neglected tropical disease infecting more than 240 million people and with 700 million people at the risk of infection in the tropical and subtropical regions of the world, especially low-income countries. For the elimination of the disease, accurate diagnostic tools are needed. Besides allowing early treatment, early detection prevents environmental contamination and in turn ensures safe water sources in the endemic areas. Cell-free DNA (cfDNA) biomarker detection is a relatively new tool, used for the diagnosis of schistosomiasis in the early stages of infection from non-invasive clinical or experimental samples. cfDNA can be detected in Schistosoma infected host body fluids such as urine, serum, saliva and tissues, mainly in blood offering significant benefits for accurate diagnosis. In the current review, we described different characteristics of cfDNA, evidencing and supporting its potential uses in Schistosoma diagnosis and the improvement of treatment effectiveness.

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来源期刊
CiteScore
2.90
自引率
0.00%
发文量
51
审稿时长
63 days
期刊介绍: The journal provides a medium for rapid publication of investigations of the molecular biology and biochemistry of parasitic protozoa and helminths and their interactions with both the definitive and intermediate host. The main subject areas covered are: • the structure, biosynthesis, degradation, properties and function of DNA, RNA, proteins, lipids, carbohydrates and small molecular-weight substances • intermediary metabolism and bioenergetics • drug target characterization and the mode of action of antiparasitic drugs • molecular and biochemical aspects of membrane structure and function • host-parasite relationships that focus on the parasite, particularly as related to specific parasite molecules. • analysis of genes and genome structure, function and expression • analysis of variation in parasite populations relevant to genetic exchange, pathogenesis, drug and vaccine target characterization, and drug resistance. • parasite protein trafficking, organelle biogenesis, and cellular structure especially with reference to the roles of specific molecules • parasite programmed cell death, development, and cell division at the molecular level.
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