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Laboratory demonstration of a prozone-like effect in HRP2-detecting malaria rapid diagnostic tests: implications for clinical management

机译:HRP2检测疟疾快速诊断测试中类似prozone的作用的实验室演示:对临床管理的意义

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Background Malaria rapid diagnostic tests (RDTs) are now widely used for prompt on-site diagnosis in remote endemic areas where reliable microscopy is absent. Aberrant results, whereby negative test results occur at high parasite densities, have been variously reported for over a decade and have led to questions regarding the reliability of the tests in clinical use. Methods In the first trial, serial dilutions of recombinant HRP2 antigen were tested on an HRP2-detectiing RDT. In a second trial, serial dilutions of culture-derived Plasmodium falciparum parasites were tested against three HRP2-detecting RDTs. Results A prozone-like effect occurred in RDTs at a high concentration of the target antigen, histidine-rich protein-2 (above 15,000 ng/ml), a level that corresponds to more than 312000 parasites per μL. Similar results were noted on three RDT products using dilutions of cultured parasites up to a parasite density of 25%. While reduced line intensity was observed, no false negative results occurred. Conclusions These results suggest that false-negative malaria RDT results will rarely occur due to a prozone-like effect in high-density infections, and other causes are more likely. However, RDT line intensity is poorly indicative of parasite density in high-density infections and RDTs should, therefore, not be considered quantitative. Immediate management of suspected severe malaria should rely on clinical assessment or microscopy. Evaluation against high concentrations of antigen should be considered in malaria RDT product development and lot-release testing, to ensure that very weak or false negative results will not occur at antigen concentrations that might be seen clinically.
机译:背景技术疟疾快速诊断测试(RDT)现在被广泛用于缺少可靠显微镜检查的偏远地方性地区的即时现场诊断。十多年来,各种各样的结果报道了异常结果,即在高寄生虫密度下出现阴性测试结果,并引起了有关测试在临床使用中的可靠性的疑问。方法在第一个试验中,在检测HRP2的RDT上检测了重组HRP2抗原的系列稀释液。在第二项试验中,针对三种检测HRP2的RDT,测试了源自培养物的恶性疟原虫寄生虫的系列稀释液。结果在高浓度的目标抗原富含组氨酸的蛋白质2(高于15,000 ng / ml)时,在RDT中会发生前区样效应,相当于每μL超过312000寄生虫。使用稀释至最高25%的寄生虫培养物的三种RDT产品,也观察到了相似的结果。虽然观察到线强度降低,但未发生假阴性结果。结论这些结果表明,由于在高密度感染中类似prozone的作用,假阴性疟疾RDT的结果将很少发生,而其他原因的可能性更大。但是,RDT谱线强度不能很好地指示高密度感染中的寄生虫密度,因此不应将RDT视为定量的。对可疑的严重疟疾的立即处理应依靠临床评估或显微镜检查。在疟疾RDT产品开发和批次释放测试中,应考虑针对高浓度抗原进行评估,以确保在临床上可能见到的抗原浓度下不会出现非常弱或假阴性的结果。

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