Centro de Biotecnología Genómica, Instituto Politécnico Nacional, Ciudad Reynosa, Tamaulipas, México.
Adv Parasitol. 2011;77:175-226. doi: 10.1016/B978-0-12-391429-3.00008-3.
Onchocerciasis has historically been one of the leading causes of infectious blindness worldwide. It is endemic to tropical regions both in Africa and Latin America and in the Yemen. In Latin America, it is found in 13 foci located in 6 different countries. The epidemiologically most important focus of onchocerciasis in the Americas is located in a region spanning the border between Guatemala and Mexico. However, the Amazonian focus straddling the border of Venezuela and Brazil is larger in overall area because the Yanomami populations are scattered over a very large geographical region. Onchocerciasis is caused by infection with the filarial parasite Onchocerca volvulus. The infection is spread through the bites of an insect vector, black flies of the genus Simulium. In Africa, the major vectors are members of the S. damnosum complex, while numerous species serve as vectors of the parasite in Latin America. Latin America has had a long history of attempts to control onchocerciasis, stretching back almost 100 years. The earliest programmes used a strategy of surgical removal of the adult parasites from affected individuals. However, because many of the adult parasites lodge in undetectable and inaccessible areas of the body, the overall effect of this strategy on the prevalence of infection was relatively minor. In 1988, a new drug, ivermectin, was introduced that effectively killed the larval stage (microfilaria) of the parasite in infected humans. As the microfilaria is both the stage that is transmitted by the vector fly and the cause of most of the pathologies associated with the infection, ivermectin opened up a new strategy for the control of onchocerciasis. Concurrent with the use of ivermectin for the treatment of onchocerciasis, a number of sensitive new diagnostic tools were developed (both serological and nucleic acid based) that provided the efficiency, sensitivity and specificity necessary to monitor the decline and eventual elimination of onchocerciasis as a result of successful control. As a result of these advances, a strategy for the elimination of onchocerciasis was developed, based upon mass distribution of ivermectin to afflicted communities for periods lasting long enough to ensure that the parasite population was placed on the road to local elimination. This strategy has been applied for the past decade to the foci in Latin America by a programme overseen by the Onchocerciasis Elimination Program for the Americas (OEPA). The efforts spearheaded by OEPA have been very successful, eliminating ocular disease caused by O. volvulus, and eliminating and interrupting transmission of the parasite in 8 of the 13 foci in the region. As onchocerciasis approaches elimination in Latin America, several questions still need to be addressed. These include defining an acceptable upper limit for transmission in areas in which transmission is thought to have been suppressed (e.g. what is the maximum value for the upper bound of the 95% confidence interval for transmission rates in areas where transmission is no longer detectable), how to develop strategies for conducting surveillance for recrudescence of infection in areas in which transmission is thought to be interrupted and how to address the problem in areas where the mass distribution of ivermectin seems to be unable to completely eliminate the infection.
盘尾丝虫病历来是全世界导致传染性失明的主要原因之一。它在非洲和拉丁美洲以及也门的热带地区流行。在拉丁美洲,有 13 个流行区分布在 6 个不同的国家。美洲最重要的盘尾丝虫病流行区位于危地马拉和墨西哥边境地区。然而,横跨委内瑞拉和巴西边境的亚马孙流行区面积更大,因为雅诺马米人分布在非常大的地理区域。盘尾丝虫病是由感染旋盘尾丝虫引起的。这种感染是通过一种昆虫媒介,即类蚋属的黑蝇的叮咬传播的。在非洲,主要的媒介是 S. damnosum 复合体的成员,而在拉丁美洲,许多物种都是寄生虫的媒介。拉丁美洲有很长的控制盘尾丝虫病的历史,可以追溯到近 100 年以前。最早的方案使用的是从受感染的个体中手术切除成虫的策略。然而,由于许多成虫都寄居在身体内无法检测和无法到达的部位,因此这种策略对感染流行率的总体影响相对较小。1988 年,引入了一种新的药物伊维菌素,它能有效地杀死感染人体内的幼虫(微丝蚴)阶段。由于微丝蚴既是媒介蝇传播的阶段,也是与感染相关的大多数病理的原因,伊维菌素为盘尾丝虫病的控制开辟了新的策略。在使用伊维菌素治疗盘尾丝虫病的同时,还开发了许多新的、敏感的诊断工具(包括血清学和基于核酸的方法),这些工具提供了监测由于成功控制而导致盘尾丝虫病下降和最终消除所需的效率、敏感性和特异性。由于这些进展,制定了消灭盘尾丝虫病的策略,该策略基于向受感染的社区大量分发伊维菌素,持续时间足以确保寄生虫种群走上局部消除的道路。过去十年来,美洲盘尾丝虫病消除方案(OEPA)一直在拉丁美洲的流行区实施这一策略。OEPA 领导的努力非常成功,消除了由旋盘尾丝虫引起的眼部疾病,并在该地区的 13 个流行区中的 8 个区消除和中断了寄生虫的传播。随着盘尾丝虫病在拉丁美洲接近消除,仍有几个问题需要解决。这些问题包括为认为已经被抑制的传播地区(例如,在传播已不再可检测的地区,传播率 95%置信区间上限的最大值是多少)定义可接受的传播上限,以及如何制定策略,对认为已经被阻断的传播地区进行感染复发的监测,以及如何解决伊维菌素大量分发似乎无法完全消除感染的地区的问题。