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首页> 外文期刊>The American Journal of Tropical Medicine and Hygiene >Development and evaluation of a rapid diagnostic test for Plasmodium falciparum, P. vivax, and mixed-species malaria antigens.
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Development and evaluation of a rapid diagnostic test for Plasmodium falciparum, P. vivax, and mixed-species malaria antigens.

机译:恶性疟原虫,间日疟原虫和混合物种疟疾抗原的快速诊断测试的开发和评估。

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摘要

Plasmodium falciparum and P. vivax malaria are endemic to many parts of the world and humans can be co-infected with both species. Because each Plasmodium species has different biological and clinical characteristics, accurate differentiation of the infecting species is essential for effective treatment. Therefore, we produced three monoclonal antibodies that recognize the lactate dehydrogenase of P. falciparum, P. vivax, or both to develop the first P. falciparum, P. vivax, and mixed-species infections malaria antigen detection kit. The detection limits of this kit were 150 and 250 parasites/muL for P. falciparum and P. vivax, respectively, and the kit was able to detect mixed-species infections. The sensitivity and specificity of this kit was assessed with 722 clinical specimens. Our results showed that its sensitivities for P. falciparum, P. vivax, and mixed-species infection were 96.5%, 95.3%, and 85.7%, respectively. In addition, its specificity was high (99.4%).
机译:恶性疟原虫和间日疟原虫是世界许多地方的地方病,人类可能同时感染这两个物种。由于每种疟原虫物种都有不同的生物学和临床特征,因此准确区分感染物种对于有效治疗至关重要。因此,我们生产了三种单克隆抗体,可识别恶性疟原虫,间日疟原虫或两者的乳酸脱氢酶,以开发第一个恶性疟原虫,间日疟原虫和混合物种感染疟疾抗原检测试剂盒。该试剂盒对于恶性疟原虫和间日疟原虫的检出限分别为150和250寄生虫/微升,该试剂盒能够检测混合物种感染。用722个临床标本评估了该试剂盒的敏感性和特异性。我们的结果表明,其对恶性疟原虫,间日疟原虫和混合物种感染的敏感性分别为96.5%,95.3%和85.7%。此外,它的特异性很高(99.4%)。

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