Fernandes A, Pereira A T M, Eschenazi P D, Schilter H C, Sousa A L S, Teixeira M M, Negrão-Corrêa D
Santa Casa de Misericórdia de Belo Horizonte, Belo Horizonte, MG, Brazil.
Parasite Immunol. 2008 Mar;30(3):139-49. doi: 10.1111/j.1365-3024.2007.01009.x. Epub 2007 Dec 18.
The present study was carried out to investigate the immune response against Strongyloides venezuelensis infection in Balb/c mice previously immunized with larva-antigens or primed with live-larvae. Our results indicate that all primed mice developed a strong protection against challenge infection that remained active for 45 days. In mice primed with live-larvae the challenge infection resulted in great reduction of migrating larvae and the worms were completely eliminated from the small intestine before maturation. The protection pattern did not alter when the primary infection was aborted by drug treatment. In these experimental groups, the challenge infection was accompanied by a type-2 predominant immune response, intense IgE and reactive IgG1 production, and granulocyte infiltration in skin, lungs and intestine. The challenge infection in antigen-immunized mice also resulted in great reduction of migrating larvae. However, the worms that reached the host intestine matured, produced eggs and were eliminated similarly to the ones from nonimmunized mice. Protective mechanisms after immunization with larva antigen were migrating larva-specific and associated with a strong and mixed Th1 and Th2 response, without tissue granulocyte infiltration. In conclusion, protective immunity induced by a previous infection or antigen-immunization are stage-specific and operate through different effector mechanisms.
本研究旨在调查先前用幼虫抗原免疫或用活幼虫致敏的Balb/c小鼠对委内瑞拉类圆线虫感染的免疫反应。我们的结果表明,所有致敏小鼠均对攻击感染产生了强大的保护作用,且这种保护作用持续45天。在用活幼虫致敏的小鼠中,攻击感染导致迁移幼虫数量大幅减少,并且蠕虫在成熟前从小肠中完全清除。当通过药物治疗中止初次感染时,保护模式并未改变。在这些实验组中,攻击感染伴随着以2型为主的免疫反应、强烈的IgE和反应性IgG1产生,以及皮肤、肺和肠道中的粒细胞浸润。在用抗原免疫的小鼠中,攻击感染也导致迁移幼虫数量大幅减少。然而,到达宿主肠道的蠕虫成熟、产卵,并与未免疫小鼠的蠕虫一样被清除。用幼虫抗原免疫后的保护机制是针对迁移幼虫的特异性机制,与强烈的混合Th1和Th2反应相关,且无组织粒细胞浸润。总之,先前感染或抗原免疫诱导的保护性免疫具有阶段特异性,并通过不同的效应机制发挥作用。