Steel Cathy, Golden Allison, Kubofcik Joseph, LaRue Nicole, de Los Santos Tala, Domingo Gonzalo J, Nutman Thomas B
Laboratory of Parasitic Diseases, National Institutes of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
Clin Vaccine Immunol. 2013 Aug;20(8):1155-61. doi: 10.1128/CVI.00252-13. Epub 2013 Jun 5.
The Global Programme to Eliminate Lymphatic Filariasis has an urgent need for rapid assays to detect ongoing transmission of lymphatic filariasis (LF) following multiple rounds of mass drug administration (MDA). Current WHO guidelines support using the antigen card immunochromatographic test (ICT), which detects active filarial infection but does not detect early exposure to LF. Recent studies found that antibody-based assays better serve this function. In the present study, two tests, a rapid IgG4 enzyme-linked immunosorbent assay (ELISA) and a lateral-flow strip immunoassay, were developed based on the highly sensitive and specific Wuchereria bancrofti antigen Wb123. A comparison of W. bancrofti-infected and -uninfected patients (with or without other helminth infections) demonstrated that both tests had high sensitivities and specificities (93 and 97% [ELISA] and 92 and 96% [strips], respectively). When the W. bancrofti-uninfected group was separated into those with other filarial/helminth infections (i.e., onchocerciasis, loiasis, and strongyloidiasis) and those who were parasite uninfected, the specificities of the assays varied between 91 and 100%. In addition, the geometric mean response by ELISA of W. bancrofti-infected patients was significantly higher than the response of those without W. bancrofti infection (P < 0.0001). Furthermore, the Wb123 ELISA and the lateral-flow strips had high positive and negative predictive values, giving valuable information on the size of survey population needed to be reasonably certain whether or not transmission is ongoing. These highly sensitive and specific IgG4 tests to the W. bancrofti Wb123 protein give every indication that they will serve as useful tools for post-MDA monitoring.
全球消除淋巴丝虫病规划迫切需要快速检测方法,以在多轮大规模药物给药(MDA)后检测淋巴丝虫病(LF)的持续传播情况。世界卫生组织现行指南支持使用抗原卡片免疫层析试验(ICT),该试验可检测活动性丝虫感染,但无法检测LF的早期暴露情况。最近的研究发现基于抗体的检测方法更适合此功能。在本研究中,基于高度敏感和特异的班氏吴策线虫抗原Wb123开发了两种检测方法,即快速IgG4酶联免疫吸附试验(ELISA)和侧向流动试纸免疫测定法。对感染和未感染班氏吴策线虫的患者(有无其他蠕虫感染)进行比较表明,两种检测方法均具有高灵敏度和特异性(ELISA分别为93%和97%,试纸法分别为92%和96%)。当将未感染班氏吴策线虫的组分为有其他丝虫/蠕虫感染(即盘尾丝虫病、罗阿丝虫病和粪类圆线虫病)的患者和未感染寄生虫的患者时,检测方法的特异性在91%至100%之间变化。此外,感染班氏吴策线虫患者的ELISA几何平均反应显著高于未感染班氏吴策线虫患者的反应(P<0.0001)。此外,Wb123 ELISA和侧向流动试纸具有高阳性和阴性预测值,可为合理确定传播是否正在进行所需的调查人群规模提供有价值的信息。这些针对班氏吴策线虫Wb123蛋白的高度敏感和特异的IgG4检测方法表明,它们将成为MDA后监测的有用工具。