Nogueira Denise Silva, Gazzinelli-Guimarães Pedro Henrique, Barbosa Fernando Sérgio, Resende Nathália Maria, Silva Caroline Cavalcanti, de Oliveira Luciana Maria, Amorim Chiara Cássia Oliveira, Oliveira Fabrício Marcus Silva, Mattos Matheus Silvério, Kraemer Lucas Rocha, Caliari Marcelo Vidigal, Gaze Soraya, Bueno Lilian Lacerda, Russo Remo Castro, Fujiwara Ricardo Toshio
Laboratory of Immunology and Parasite Genomics, Department of Parasitology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Institute of Biological and Health Sciences, Universidade Federal do Mato Grosso, Cuiabá, Brazil.
PLoS Negl Trop Dis. 2016 Jan 27;10(1):e0004382. doi: 10.1371/journal.pntd.0004382. eCollection 2016 Jan.
Ascaris spp. infection affects 800 million people worldwide, and half of the world population is currently at risk of infection. Recurrent reinfection in humans is mostly due to the simplicity of the parasite life cycle, but the impact of multiple exposures to the biology of the infection and the consequences to the host's homeostasis are poorly understood. In this context, single and multiple exposures in mice were performed in order to characterize the parasitological, histopathological, tissue functional and immunological aspects of experimental larval ascariasis. The most important findings revealed that reinfected mice presented a significant reduction of parasite burden in the lung and an increase in the cellularity in the bronchoalveolar lavage (BAL) associated with a robust granulocytic pulmonary inflammation, leading to a severe impairment of respiratory function. Moreover, the multiple exposures to Ascaris elicited an increased number of circulating inflammatory cells as well as production of higher levels of systemic cytokines, mainly IL-4, IL-5, IL-6, IL-10, IL-17A and TNF-α when compared to single-infected animals. Taken together, our results suggest the intense pulmonary inflammation associated with a polarized systemic Th2/Th17 immune response are crucial to control larval migration after multiple exposures to Ascaris.
蛔虫属感染影响着全球8亿人,目前世界上一半的人口面临感染风险。人类反复再感染主要是由于寄生虫生命周期简单,但多次接触感染生物学及其对宿主内环境稳态的影响却知之甚少。在此背景下,在小鼠中进行了单次和多次接触实验,以表征实验性幼虫蛔虫病的寄生虫学、组织病理学、组织功能和免疫学方面。最重要的发现表明,再次感染的小鼠肺部寄生虫负荷显著降低,支气管肺泡灌洗(BAL)中的细胞数量增加,伴有强烈的粒细胞性肺部炎症,导致呼吸功能严重受损。此外,与单次感染动物相比,多次接触蛔虫会使循环炎症细胞数量增加,并产生更高水平的全身细胞因子,主要是IL-4、IL-5、IL-6、IL-10、IL-17A和TNF-α。综上所述,我们的结果表明,与极化的全身Th2/Th17免疫反应相关的强烈肺部炎症对于多次接触蛔虫后控制幼虫迁移至关重要。