Dedkova L M, Gladkova S V, Bormotov N I, Tkachenko T N, Belanov E F
Med Parazitol (Mosk). 2000 Jan-Mar(1):20-4.
The major proteins of T. gondii excretory and secretory antigens (ESA) obtained during cultivation of tachyzoites by using cultured Vero cells were shown to have molecular weights of 79, 70, 57, 48, 36, and 29 kD. ESA and somatic antigen immunoblotting demonstrated that there were noticeable differences in the immunoactive proteins of these antigens. The antibodies of the sera of patients with toxoplasmosis mainly interacted with ESA proteins having molecular weights of 79, 70, 57, 48, 36, and 29 kD, 57-kD ESA protein antibodies being present on the immunoblots of all the tested sera. When ESA was used as an antigen during enzyme immunoassay, it showed a high sensitivity in the detection of IgM antigens in congenital toxoplasmosis. At the same time, ESA identified the antibodies of this class in the sera of healthy donors much infrequently than somatic antigen (p < 0.05).
通过培养Vero细胞来培养速殖子,从而获得的弓形虫排泄和分泌抗原(ESA)的主要蛋白质,其分子量显示为79、70、57、48、36和29 kD。ESA和体细胞抗原免疫印迹表明,这些抗原的免疫活性蛋白存在明显差异。弓形虫病患者血清中的抗体主要与分子量为79、70、57、48、36和29 kD的ESA蛋白相互作用,57-kD ESA蛋白抗体存在于所有检测血清的免疫印迹中。当在酶免疫测定中使用ESA作为抗原时,它在先天性弓形虫病IgM抗原的检测中显示出高灵敏度。同时,与体细胞抗原相比,ESA在健康供体血清中很少能识别出此类抗体(p < 0.05)。