Department of Pathology, University of Cambridge, United Kingdom.
J Infect Dis. 2014 Jun 1;209(11):1792-800. doi: 10.1093/infdis/jit826. Epub 2013 Dec 19.
Human type 2 cytokine responsiveness to schistosome antigens increases after treatment; due either to removal of the immunosuppressive effects of active infection or immunological boosting by antigens released from dying parasites. We determined the responsiveness to Schistosoma mansoni over a 2-year period, when reinfection was restricted by interrupting transmission.
The proinflammatory and type 2 responses of Kenyan schoolchildren were measured before, and 1 year and 2 years posttreatment in whole blood cultures stimulated with soluble egg antigen (SEA) or soluble worm antigen (SWA). The site of S. mansoni transmission was molluscicided throughout.
Pretreatment proinflammatory responses to SEA were high but reduced 1 and 2 years posttreatment, whereas type 2 responses were low pretreatment and increased 1 and 2 years posttreatment. Type 2 responses to SWA were high pretreatment and increased at 1 year, with no further increases at 2 years posttreatment. Children infected at follow-up had lower SEA, but not SWA, posttreatment type 2 responsiveness. Increases at 1 year in type 2 SWA, but not SEA, responsiveness correlated with pretreatment egg counts.
Removal of immunosuppressive effects of active infection increases SEA type 2 responsiveness; long-term SWA type 2 responsiveness is due to treatment-induced immunological boosting. Dissociation of type 2 responses potentially protects against severe egg-associated immunopathology during infection, while allowing worm-antigen derived immunity to develop.
人体对血吸虫抗原的 2 型细胞因子反应性在治疗后会增加;这可能是由于消除了活动性感染的免疫抑制作用,或者是由于从死亡寄生虫释放的抗原引起的免疫增强作用。我们在两年的时间里确定了对曼氏血吸虫的反应性,在此期间,通过中断传播来限制再感染。
在肯尼亚学童接受治疗前、治疗后 1 年和 2 年,用可溶性卵抗原(SEA)或可溶性虫抗原(SWA)刺激全血培养物,测量其前炎症和 2 型反应。整个血吸虫传播地点都进行了灭螺处理。
SEA 的预处理前炎症反应较高,但在治疗后 1 年和 2 年降低,而 2 型反应在预处理时较低,在治疗后 1 年和 2 年增加。SWA 的 2 型反应在预处理时较高,并在 1 年时增加,在治疗后 2 年时没有进一步增加。在随访中感染的儿童的 SEA 治疗后 2 型反应较低,但 SWA 则不然。治疗后 1 年时,2 型 SWA 的反应增加,但 SEA 则没有,这与预处理时的卵计数相关。
消除活动性感染的免疫抑制作用会增加 SEA 的 2 型反应性;长期的 SWA 2 型反应性是由于治疗引起的免疫增强作用。2 型反应的分离可能有助于在感染期间防止严重的与卵相关的免疫病理学,同时允许发展出蠕虫抗原衍生的免疫力。