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循环阳极抗原(CAA):一种高灵敏度的诊断生物标志物,用于检测活动性感染-在 SCORE 期间的改进和使用。

Circulating Anodic Antigen (CAA): A Highly Sensitive Diagnostic Biomarker to Detect Active Infections-Improvement and Use during SCORE.

机构信息

1Department of Cell and Chemical Biology, Leiden University Medical Center, Leiden, Netherlands.

2Swiss Tropical and Public Health Institute, Basel, Switzerland.

出版信息

Am J Trop Med Hyg. 2020 Jul;103(1_Suppl):50-57. doi: 10.4269/ajtmh.19-0819.

Abstract

The Schistosomiasis Consortium for Operational Research and Evaluation (SCORE) was funded in 2008 to conduct research that would support country schistosomiasis control programs. As schistosomiasis prevalence decreases in many places and elimination is increasingly within reach, a sensitive and specific test to detect infection with and has become a pressing need. After obtaining broad input, SCORE supported Leiden University Medical Center (LUMC) to modify the serum-based antigen assay for use with urine, simplify the assay, and improve its sensitivity. The urine assay eventually contributed to several of the larger SCORE studies. For example, in Zanzibar, we demonstrated that urine filtration, the standard parasite egg detection diagnostic test for , greatly underestimated prevalence in low-prevalence settings. In Burundi and Rwanda, the circulating anodic antigen (CAA) assay provided critical information about the limitations of the stool-based Kato-Katz parasite egg-detection assay for in low-prevalence settings. Other SCORE-supported CAA work demonstrated that frozen, banked urine specimens yielded similar results to fresh ones; pooling of specimens may be a useful, cost-effective approach for surveillance in some settings; and the assay can be performed in local laboratories equipped with adequate centrifuge capacity. These improvements in the assay continue to be of use to researchers around the world. However, additional work will be needed if widespread dissemination of the CAA assay is to occur, for example, by building capacity in places besides LUMC and commercialization of the assay. Here, we review the evolution of the CAA assay format during the SCORE period with emphasis on urine-based applications.

摘要

血吸虫病操作研究与评价联盟(SCORE)于 2008 年成立,旨在开展支持国家血吸虫病控制规划的研究。随着许多地方血吸虫病的流行率下降,消除该病的目标越来越近,因此迫切需要一种能够灵敏且特异检测 和 感染的检测方法。在广泛征求意见后,SCORE 支持莱顿大学医学中心(LUMC)修改基于血清的抗原检测方法,以用于尿液检测,简化检测方法并提高其灵敏度。尿液检测最终为多项 SCORE 大型研究做出了贡献。例如,在桑给巴尔,我们发现尿液过滤(用于检测 的标准寄生虫卵检测诊断方法)在低流行地区大大低估了感染率。在布隆迪和卢旺达,循环阳极抗原(CAA)检测为 在低流行地区基于粪便的加藤氏厚涂片法检测寄生虫卵的局限性提供了重要信息。SCORE 支持的其他 CAA 研究表明,冷冻、储存的尿液标本与新鲜标本产生的结果相似;在某些情况下,标本混合可能是一种有用且具有成本效益的监测方法;并且该检测可以在配备足够离心能力的当地实验室中进行。这些检测方法的改进继续为世界各地的研究人员提供帮助。然而,如果要广泛传播 CAA 检测方法,例如在 LUMC 以外的地方建立能力和实现该检测方法的商业化,还需要开展更多的工作。在这里,我们重点介绍了 SCORE 期间 CAA 检测方法的演变,强调了基于尿液的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84be/7351307/07a327a50426/tpmd190819f1.jpg

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