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新型基于特异性 IgA 检测的登革热诊断商业快速检测试验评估。

Evaluation of a novel commercial rapid test for dengue diagnosis based on specific IgA detection.

机构信息

Departamento de Virología, Centro de Investigación y Estudios Avanzados del Instituto Politécnico Nacional (CINVESTAV-IPN), Mexico D.F., Mexico.

出版信息

Diagn Microbiol Infect Dis. 2012 Feb;72(2):150-5. doi: 10.1016/j.diagmicrobio.2011.11.002.

Abstract

The performance of the novel commercial test ASSURE® Dengue IgA Rapid test (MP Diagnostics) was evaluated using a panel of 172 sera collected from dengue patients and 47 sera from healthy blood donors. The overall specificity and sensitivity were 61.0% and 85.1%, respectively. However, the positivity rate for IgA went from 33.3% for sera collected the same day of fever onset to 81.2% for sera collected 5 days after fever onset. Infections with serotype 2 viruses were detected more efficiently than those with serotype 1 viruses, and no sera from infections with serotypes 3 and 4 were available. In addition, the kit was twice more efficient at detecting secondary infections than at detecting primary infections. Finally, the ASSURE® test showed good repeatability and reproducibility. The results of this study suggest that the ASSURE® Dengue IgA Rapid test may become a useful and easy-to-use test for early dengue diagnosis.

摘要

该新型商业化检测 ASSURE® Dengue IgA 快速检测试剂盒(MP 诊断公司)的性能,使用从登革热患者中收集的 172 份血清和 47 份健康献血者血清的检测板进行了评估。总体特异性和敏感性分别为 61.0%和 85.1%。然而,IgA 的阳性率从发热当天采集的血清的 33.3%上升到发热后 5 天采集的血清的 81.2%。与血清型 1 病毒感染相比,血清型 2 病毒感染的检测效率更高,而无法获得血清型 3 和 4 感染的血清。此外,该试剂盒在检测二次感染时的效率是检测初次感染时的两倍。最后,ASSURE®检测表现出良好的可重复性和再现性。本研究结果表明,ASSURE® Dengue IgA 快速检测试剂盒可能成为一种有用且易于使用的早期登革热诊断检测方法。

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