Severi M A, Ferragut G, Nieto A
Laboratoria de Inmunología Regional Norte sede Salto, Universidad de la República, Uruguay.
Parasite Immunol. 1997 Dec;19(12):545-52. doi: 10.1046/j.1365-3024.1997.d01-172.x.
The antibody response was followed during 68 weeks in 17 Balb/c mice intraperitoneally (i.p.) infected with Echinococcus granulosus protoscoleces (PSC) and in three mice i.p. immunized with dead PSC. Titres of antibodies recognizing peptidic and glucidic PSC epitopes, as well as their isotypic and avidity profiles were followed by ELISA. In addition, antigen recognition patterns were analysed by immunoblot. The response against carbohydrate epitopes was dominant in infected and immunized mice but stronger in the first group. Infected mice showed similar profiles of specific IgG and IgM with maximum titres from week 38 to 53. Although IgG1 and IgG3 were the predominant antibody subclasses, the ratio of IgG1/IgG3 antibody titres as well as antibody avidity decreased during the experiment, encompassing a decrease in recognition of peptidic epitopes. Immunized mice did not show significant levels of specific IgM and, after week 15, showed IgG titres lower than the infected mice. IgG1 was the predominant IgG subclass during all the experiment with background levels of IgG3. The mean Ab avidity was high and showed no significant changes during immunization. Different patterns of response were thus produced by dead and developing live parasites. Although high avidity IgG1 antibodies were early found in both cases, lower avidity IgG3 antibodies were increasingly produced afterwards only in infected animals. The isotype switch and avidity decrease observed only during infection are consistent with a possible parasitic mechanism to evade host immunity.
在17只经腹腔感染细粒棘球绦虫原头节(PSC)的Balb/c小鼠以及3只经腹腔注射死PSC免疫的小鼠中,持续68周观察其抗体反应。通过ELISA追踪识别肽类和糖类PSC表位的抗体滴度,以及它们的同种型和亲和力谱。此外,通过免疫印迹分析抗原识别模式。在感染和免疫的小鼠中,针对碳水化合物表位的反应占主导,但在第一组中更强。感染小鼠显示出相似的特异性IgG和IgM谱,在第38周至53周达到最高滴度。虽然IgG1和IgG3是主要的抗体亚类,但在实验过程中,IgG1/IgG3抗体滴度的比值以及抗体亲和力均下降,包括对肽类表位识别的减少。免疫小鼠未显示出显著水平的特异性IgM,在第15周后,其IgG滴度低于感染小鼠。在整个实验过程中,IgG1是主要的IgG亚类,IgG3处于背景水平。平均抗体亲和力较高,在免疫过程中未显示出显著变化。因此,死寄生虫和正在发育的活寄生虫产生了不同的反应模式。虽然在两种情况下均早期发现了高亲和力的IgG1抗体,但仅在感染动物中,随后越来越多地产生了低亲和力的IgG3抗体。仅在感染期间观察到的同种型转换和亲和力下降与寄生虫逃避宿主免疫的可能机制一致。