Institut de Recherche pour le Développement, Unité Mixte de Recherche IRD-CIRAD 177, Campus International de Baillarguet, Montpellier, France.
PLoS Negl Trop Dis. 2012;6(6):e1691. doi: 10.1371/journal.pntd.0001691. Epub 2012 Jun 12.
The final outcome of infection by Trypanosoma brucei gambiense, the main agent of sleeping sickness, has always been considered as invariably fatal. While scarce and old reports have mentioned cases of self-cure in untreated patients, these studies suffered from the lack of accurate diagnostic tools available at that time. Here, using the most specific and sensitive tools available to date, we report on a long-term follow-up (15 years) of a cohort of 50 human African trypanosomiasis (HAT) patients from the Ivory Coast among whom 11 refused treatment after their initial diagnosis. In 10 out of 11 subjects who continued to refuse treatment despite repeated visits, parasite clearance was observed using both microscopy and polymerase chain reaction (PCR). Most of these subjects (7/10) also displayed decreasing serological responses, becoming progressively negative to trypanosome variable antigens (LiTat 1.3, 1.5 and 1.6). Hence, in addition to the "classic" lethal outcome of HAT, we show that alternative natural progressions of HAT may occur: progression to an apparently aparasitaemic and asymptomatic infection associated with strong long-lasting serological responses and progression to an apparently spontaneous resolution of infection (with negative results in parasitological tests and PCR) associated with a progressive drop in antibody titres as observed in treated cases. While this study does not precisely estimate the frequency of the alternative courses for this infection, it is noteworthy that in the field national control programs encounter a significant proportion of subjects displaying positive serologic test results but negative results in parasitological testing. These findings demonstrate that a number of these subjects display such infection courses. From our point of view, recognising that trypanotolerance exists in humans, as is now widely accepted for animals, is a major step forward for future research in the field of HAT.
冈比亚锥虫(引起昏睡病的主要病原体)感染的最终结果一直被认为是不可避免的致命。尽管有少量且陈旧的报告提到未经治疗的患者有自愈的情况,但这些研究受到当时缺乏准确诊断工具的限制。在这里,我们使用目前最特异和敏感的工具,报告了来自科特迪瓦的一组 50 例人类非洲锥虫病(HAT)患者的长期随访(15 年),其中 11 例在初始诊断后拒绝治疗。在 11 例继续拒绝治疗的患者中,尽管多次就诊,但仍通过显微镜和聚合酶链反应(PCR)观察到寄生虫清除。在继续拒绝治疗的 10 例患者中,大多数(7/10)也表现出血清学反应逐渐下降,对锥虫可变抗原(LiTat 1.3、1.5 和 1.6)的反应逐渐转为阴性。因此,除了 HAT 的“经典”致死结果外,我们还表明 HAT 可能出现替代的自然进展:进展为明显无寄生虫血症和无症状感染,并伴有强烈的长期血清学反应,以及进展为感染的自发消退(寄生虫学检测和 PCR 均为阴性),并伴有抗体滴度逐渐下降,如在治疗病例中观察到的那样。虽然本研究不能精确估计这种感染的替代病程的频率,但值得注意的是,在现场,国家控制计划遇到了相当一部分表现出阳性血清学检测结果但寄生虫学检测结果为阴性的患者。这些发现表明,许多患者表现出这种感染的病程。从我们的角度来看,认识到人类存在对锥虫的耐受,就像现在广泛接受的动物一样,是人类非洲锥虫病领域未来研究的一个重大进展。