Department of Pathobiology and Population Sciences and London Centre for Neglected Tropical Disease Research, Royal Veterinary College, Hatfield.
Department of Infectious Disease Epidemiology and London Centre for Neglected Tropical Disease Research, Imperial College London, United Kingdom.
Clin Infect Dis. 2017 Nov 29;65(12):2026-2034. doi: 10.1093/cid/cix616.
Mass drug administration (MDA) with ivermectin is the cornerstone of efforts to eliminate human onchocerciasis by 2020 or 2025. The feasibility of elimination crucially depends on the effects of multiple ivermectin doses on Onchocerca volvulus. A single ivermectin (standard) dose clears the skin-dwelling microfilarial progeny of adult worms (macrofilariae) and temporarily impedes the release of such progeny by female macrofilariae, but a macrofilaricidal effect has been deemed minimal. Multiple doses of ivermectin may cumulatively and permanently reduce the fertility and shorten the lifespan of adult females. However, rigorous quantification of these effects necessitates interrogating longitudinal data on macrofilariae with suitably powerful analytical techniques.
Using a novel mathematical modeling approach, we analyzed, at an individual participant level, longitudinal data on viability and fertility of female worms from the single most comprehensive multiple-dose clinical trial of ivermectin, comparing 3-monthly with annual treatments administered for 3 years in Cameroon.
Multiple doses of ivermectin have a partial macrofilaricidal and a modest permanent sterilizing effect after 4 or more consecutive treatments, even at routine MDA doses (150 µg/kg) and frequencies (annual). The life expectancy of adult O. volvulus is reduced by approximately 50% and 70% after 3 years of annual or 3-monthly (quarterly) exposures to ivermectin.
Our quantification of macrofilaricidal and sterilizing effects of ivermectin should be incorporated into transmission models to inform onchocerciasis elimination efforts in Africa and residual foci in Latin America. It also provides a framework to assess macrofilaricidal candidate drugs currently under development.
大规模药物治疗(MDA)用伊维菌素是到 2020 年或 2025 年消除人体盘尾丝虫病的基石。消除的可行性主要取决于多次伊维菌素剂量对盘尾丝虫的影响。单次伊维菌素(标准)剂量可清除成虫(大丝虫)在皮肤中寄居的微丝蚴后代,并暂时阻止雌性大丝虫释放此类后代,但被认为微丝蚴杀伤力极小。多次伊维菌素剂量可能会累积并永久降低雌性成虫的生育能力并缩短其寿命。然而,严格量化这些影响需要利用适当强大的分析技术来检测大丝虫的纵向数据。
我们采用一种新颖的数学建模方法,在个体参与者水平上分析了来自单次最全面的伊维菌素多次剂量临床试验的女性蠕虫的存活力和生育力的纵向数据,该试验在喀麦隆比较了每 3 个月和每年治疗 3 年的效果。
多次伊维菌素剂量在连续 4 次以上治疗后,即使在常规 MDA 剂量(150μg/kg)和频率(每年)下,也具有部分杀微丝蚴和适度的永久绝育作用。在每年或每 3 个月(每季度)接触伊维菌素 3 年后,成年盘尾丝虫的预期寿命缩短了约 50%和 70%。
我们对伊维菌素的杀微丝蚴和绝育作用的量化应纳入传播模型,以指导非洲的盘尾丝虫病消除工作和拉丁美洲的残留焦点。它还为评估目前正在开发的杀微丝蚴候选药物提供了一个框架。