Golden Allison, Stevens Eric J, Yokobe Lindsay, Faulx Dunia, Kalnoky Michael, Peck Roger, Valdez Melissa, Steel Cathy, Karabou Potochoziou, Banla Méba, Soboslay Peter T, Adade Kangi, Tekle Afework H, Cama Vitaliano A, Fischer Peter U, Nutman Thomas B, Unnasch Thomas R, de los Santos Tala, Domingo Gonzalo J
Diagnostics Global Program, PATH, Seattle, Washington, United States of America.
Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, United States of America.
PLoS Negl Trop Dis. 2016 Jan 8;10(1):e0004292. doi: 10.1371/journal.pntd.0004292. eCollection 2016 Jan.
Serological assays for human IgG4 to the Onchocerca volvulus antigen Ov16 have been used to confirm elimination of onchocerciasis in much of the Americas and parts of Africa. A standardized source of positive control antibody (human anti-Ov16 IgG4) will ensure the quality of surveillance data using these tests.
METHODOLOGY/PRINCIPAL FINDINGS: A recombinant human IgG4 antibody to Ov16 was identified by screening against a synthetic human Fab phage display library and converted into human IgG4. This antibody was developed into different positive control formulations for enzyme-linked immunosorbent assay (ELISA) and rapid diagnostic test (RDT) platforms. Variation in ELISA results and utility as a positive control of the antibody were assessed from multiple laboratories. Temperature and humidity conditions were collected across seven surveillance activities from 2011-2014 to inform stability requirements for RDTs and positive controls. The feasibility of the dried positive control for RDT was evaluated during onchocerciasis surveillance activity in Togo, in 2014. When the anti-Ov16 IgG4 antibody was used as a standard dilution in horseradish peroxidase (HRP) and alkaline phosphatase (AP) ELISAs, the detection limits were approximately 1ng/mL by HRP ELISA and 10ng/mL by AP ELISA. Positive control dilutions and spiked dried blood spots (DBS) produced similar ELISA results. Used as a simple plate normalization control, the positive control antibody may improve ELISA data comparison in the context of inter-laboratory variation. The aggregate temperature and humidity monitor data informed temperature parameters under which the dried positive control was tested and are applicable inputs for testing of diagnostics tools intended for sub-Saharan Africa. As a packaged positive control for Ov16 RDTs, stability of the antibody was demonstrated for over six months at relevant temperatures in the laboratory and for over 15 weeks under field conditions.
The recombinant human anti-Ov16 IgG4 antibody-based positive control will benefit inter-laboratory validation of ELISA assays and serve as quality control (QC) reagents for Ov16 RDTs at different points of the supply chain from manufacturer to field use.
针对盘尾丝虫抗原Ov16的人IgG4血清学检测已被用于确认美洲大部分地区和非洲部分地区盘尾丝虫病的消除情况。标准化的阳性对照抗体(人抗Ov16 IgG4)来源将确保使用这些检测方法的监测数据质量。
方法/主要发现:通过筛选合成人Fab噬菌体展示文库鉴定出一种针对Ov16的重组人IgG4抗体,并将其转化为人IgG4。该抗体被开发成用于酶联免疫吸附测定(ELISA)和快速诊断检测(RDT)平台的不同阳性对照制剂。从多个实验室评估了ELISA结果的差异以及该抗体作为阳性对照的效用。收集了2011年至2014年期间七次监测活动的温度和湿度条件,以确定RDT和阳性对照的稳定性要求。2014年在多哥的盘尾丝虫病监测活动中评估了用于RDT的干燥阳性对照的可行性。当抗Ov16 IgG4抗体用作辣根过氧化物酶(HRP)和碱性磷酸酶(AP)ELISA的标准稀释液时,HRP ELISA的检测限约为1ng/mL,AP ELISA的检测限约为10ng/mL。阳性对照稀释液和加标的干血斑(DBS)产生了相似的ELISA结果。用作简单的板标准化对照时,阳性对照抗体可改善实验室间差异情况下的ELISA数据比较。汇总的温度和湿度监测数据提供了测试干燥阳性对照的温度参数,并且是用于撒哈拉以南非洲诊断工具测试的适用输入。作为Ov16 RDT的包装阳性对照,该抗体在实验室相关温度下的稳定性证明超过六个月,在现场条件下超过15周。
基于重组人抗Ov16 IgG4抗体的阳性对照将有利于ELISA检测的实验室间验证,并作为从制造商到现场使用的供应链不同环节Ov16 RDT的质量控制(QC)试剂。