Negrão-Corrêa Deborah, Silveira Micheline R, Borges Cynthia M, Souza Danielle G, Teixeira Mauro M
Departamento de Parasitologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Infect Immun. 2003 May;71(5):2607-14. doi: 10.1128/IAI.71.5.2607-2614.2003.
The prevalence of allergic diseases such as asthma has increased markedly over the past few decades. To evaluate the possible mutual influence of helminth infection and allergy, the combined effects of experimental allergic airway inflammation and infection with Strongyloides venezuelensis on various parasitological and inflammatory indices were evaluated in the rat. A challenge of immunized rats with aerosolized ovalbumin (OVA) resulted in eosinophilic inflammation that peaked 48 h after the challenge and was accompanied by airway hyperresponsiveness (AHR) to an intravenous acetylcholine challenge. S. venezuelensis infection concomitant with an OVA challenge of immunized rats resulted in prolonged pulmonary inflammation with increased eosinophil infiltration in bronchoalveolar lavage fluid but not in the lung tissue. These rats also showed a significant parasite burden reduction, especially during parasite migration through the lungs. However, the fecundity rates of worms that reached the intestine were similar in allergic and nonallergic animals. Despite airway inflammation, the increased responsiveness of the airways in the experimental asthma model was suppressed during parasite migration through the lungs (2 days). In contrast, parasite-induced AHR was unchanged 5 days after infection in immunized and challenged rats. In conclusion, infection with S. venezuelensis interfered with the onset of AHR following an antigen challenge of immunized rats. The ability of parasites to switch off functional airway responses is therapeutically relevant because we may learn from parasites how to modulate lung function and, hence, the AHR characteristic of asthmatic patients.
在过去几十年中,哮喘等过敏性疾病的患病率显著上升。为了评估蠕虫感染与过敏之间可能的相互影响,我们在大鼠中评估了实验性过敏性气道炎症和委内瑞拉类圆线虫感染对各种寄生虫学和炎症指标的综合影响。用雾化卵清蛋白(OVA)攻击免疫大鼠会导致嗜酸性炎症,在攻击后48小时达到峰值,并伴有对静脉注射乙酰胆碱攻击的气道高反应性(AHR)。在免疫大鼠接受OVA攻击的同时感染委内瑞拉类圆线虫,会导致肺部炎症延长,支气管肺泡灌洗液中的嗜酸性粒细胞浸润增加,但肺组织中没有。这些大鼠的寄生虫负担也显著降低,尤其是在寄生虫通过肺部迁移期间。然而,到达肠道的蠕虫的繁殖率在过敏和非过敏动物中相似。尽管存在气道炎症,但在寄生虫通过肺部迁移期间(2天),实验性哮喘模型中气道的反应性增加受到抑制。相比之下,在免疫和攻击的大鼠中,感染后5天寄生虫诱导的AHR没有变化。总之,委内瑞拉类圆线虫感染干扰了免疫大鼠抗原攻击后AHR的发作。寄生虫关闭功能性气道反应的能力在治疗上具有相关性,因为我们可以从寄生虫身上学习如何调节肺功能,从而调节哮喘患者的AHR特征。