Kang Keren, Dzakah Emmanuel E, Huang Yongping, Xie Mingquan, Luo Xiaochun, Li Wenmei, Wang Jihua
School of Bioscience and Bioengineering, South China University of Technology, Guangzhou, 510006, Guangdong, China.
National Engineering Laboratory of Rapid Diagnostic Tests, Guangzhou Wondfo Biotech Co Ltd, Guangzhou, 510663, Guangdong, China.
Malar J. 2015 May 30;14:228. doi: 10.1186/s12936-015-0740-1.
The low sensitivity and specificity of Plasmodium falciparum diagnostic tests pose a serious health threat to people living in endemic areas. The objective of the study was to develop a rapid assay for the detection of histidine-rich protein 2 (HRP2) of P. falciparum in whole blood by immunofluorescence chromatographic technology.
A total of 1163 positive and negative blood samples were screened. The double-antibody sandwich assay was used to establish the kit and its performance was evaluated for sensitivity, specificity, accuracy, precision, stability, and clinical effectiveness.
The cut-off level of detection of the kit was 25 parasites/μl. Common interfering substances in human blood specimens, such as bilirubin, triglyceride and cholesterol had no significant effect on HRP2 antigen detection. The precision of the kit was run with different concentration of standard calibrators and the values were less than 10 %. The performance of this diagnostic kit in the detection of the calibrators has shown that a shelf life of about 12 months gives a more reliable result. Among clinical samples tested, the HRP2 test kit and the reference products had good coincidence rate in a parallel experiment and this test kit had a more sensitive detecting level to the target protein than the reference kits used in this study. The specificity and sensitivity for this test were 99.6 % (800/803) and 99.7 % (1160/1163), respectively.
A novel HRP2 immunofluorescence detection method was developed in this study. Overall performance evaluation indicated that the kit has a rapid, high sensitivity and on-spot method for detecting P. falciparum.
恶性疟原虫诊断检测的低灵敏度和特异性对流行地区的居民构成了严重的健康威胁。本研究的目的是通过免疫荧光色谱技术开发一种用于检测全血中恶性疟原虫富含组氨酸蛋白2(HRP2)的快速检测方法。
共筛选了1163份阳性和阴性血样。采用双抗体夹心测定法建立试剂盒,并对其灵敏度、特异性、准确性、精密度、稳定性和临床有效性进行评估。
该试剂盒的检测临界值为25个寄生虫/微升。人血标本中的常见干扰物质,如胆红素、甘油三酯和胆固醇,对HRP2抗原检测无显著影响。用不同浓度的标准校准品对试剂盒进行精密度检测,其值均小于10%。该诊断试剂盒在检测校准品时的性能表明,约12个月的保质期能给出更可靠的结果。在检测的临床样本中,HRP2检测试剂盒与参比产品在平行试验中具有良好的符合率,且该检测试剂盒对目标蛋白的检测水平比本研究中使用的参比试剂盒更灵敏。该检测方法的特异性和灵敏度分别为99.6%(800/803)和99.7%(1160/1163)。
本研究开发了一种新型的HRP2免疫荧光检测方法。总体性能评估表明,该试剂盒是一种用于检测恶性疟原虫的快速、高灵敏度的现场检测方法。