Iglesias R, Leiro J, Ubeira F M, Santamarina M T, Sanmartín M L
Departamento di Microbiologia y Parasitología, Facultad de Farmacia, Universidad de Santiago de Compostela, La Coruña, Spain.
Parasite Immunol. 1993 May;15(5):243-50. doi: 10.1111/j.1365-3024.1993.tb00607.x.
The kinetics of antibody response to intraperitoneal infection of mice with third stage larvae of Anisakis simplex was investigated by ELISA. Maximum antibody response to excretion-secretion (ES) antigens was reached before maximum response to somatic (SA) antigens. Total immunoglobulin (Ig) production (consisting mainly of IgM and IgG1 isotypes) was very similar in both cases. Immunoblotting was used to characterize the antigens recognized by the host in the presence or absence of the metabolic products released by the parasite in vivo. Sera from mice infected with live larvae (anti-L3 L serum) and immunized with dead larvae (anti-L3 D serum) recognized a similar pattern of bands in immunoblots of ES and SA antigen preparations. In the latter, however, three bands at 14, 17 and 18 kD were only recognized by the anti-L3 L serum. A possible explanation is that these low molecular weight antigens are ES products released only in vivo. Finally, the immune response in mouse was compared using ELISA and immunoblotting with the response of a human anisakiasis reference serum, and was found to display considerable similarities. This suggests that the mouse may be a useful model for studying the immunobiology of A. simplex in man.
通过酶联免疫吸附测定(ELISA)研究了小鼠经单殖吸虫第三期幼虫腹腔感染后抗体反应的动力学。对排泄-分泌(ES)抗原的最大抗体反应在对虫体(SA)抗原的最大反应之前达到。两种情况下总免疫球蛋白(Ig)产生(主要由IgM和IgG1同种型组成)非常相似。免疫印迹用于鉴定在存在或不存在寄生虫在体内释放的代谢产物的情况下宿主识别的抗原。感染活幼虫的小鼠血清(抗L3 L血清)和用死幼虫免疫的小鼠血清(抗L3 D血清)在ES和SA抗原制剂的免疫印迹中识别出相似的条带模式。然而,在后者中,14、17和18 kD的三条带仅被抗L3 L血清识别。一种可能的解释是这些低分子量抗原是仅在体内释放的ES产物。最后,使用ELISA和免疫印迹将小鼠中的免疫反应与人旋毛虫病参考血清的反应进行比较,发现显示出相当大的相似性。这表明小鼠可能是研究人单殖吸虫免疫生物学的有用模型。