Handali Sukwan, Gonzalez Armando E, Hancock Kathy, Garcia Hector H, Roberts Jacquelin M, Gilman Robert H, Tsang Victor C W
Immunology Branch, Division of Parasitic Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia 30341-3724, USA.
Am J Trop Med Hyg. 2004 Sep;71(3):322-6.
Cysticercosis, a disease caused by the larval form of Taenia solium, is diagnosed by detection of specific antibodies or by imaging techniques. Our preferred immunologic assay for cysticercosis is the enzyme-linked immunoelectrodifusion transfer blot, or immunoblot, using the lentil lectin bound antigens from larval cysts. Antibody reactivity with any one of seven glycoproteins is diagnostic for cysticercosis. To develop a simple antibody detection assay for field use, we have synthesized an 8-kD diagnostic antigen, sTs18var1 (a secreted protein with a mature size of 67 amino acids), and expressed a 50-kD membrane protein antigen, rGp50. We used these two diagnostic proteins in a quantitative Falcon assay screening test-enzyme-linked immunosorbent assay (FAST-ELISA) to measure the antibody responses in Peruvian pigs with cysticercosis. Three study designs were used. First, we followed the kinetics of antibody responses against these two diagnostic proteins in pigs with cysticercosis that were treated with oxfendazole. Second, we measured antibody response in naive experimentally infected pigs. Third, we followed the maternal antibodies against rGp50 and sTs18var1 in piglets born from sows with cysticercosis. These studies showed that antibody responses against the two diagnostic proteins in the FAST-ELISA are quantitatively correlated with infection by viable cysts, with anti-sTs18var1 activity being most responsive to the status of infection.
囊尾蚴病是由猪带绦虫幼虫引起的疾病,可通过检测特异性抗体或成像技术进行诊断。我们用于囊尾蚴病的首选免疫测定方法是酶联免疫电扩散转移印迹法,即免疫印迹法,使用来自幼虫囊肿的扁豆凝集素结合抗原。与七种糖蛋白中任何一种的抗体反应性可诊断囊尾蚴病。为了开发一种适用于现场使用的简单抗体检测方法,我们合成了一种8-kD诊断抗原sTs18var1(一种成熟大小为67个氨基酸的分泌蛋白),并表达了一种50-kD膜蛋白抗原rGp50。我们在定量Falcon检测筛选试验-酶联免疫吸附测定法(FAST-ELISA)中使用这两种诊断蛋白来测量患有囊尾蚴病的秘鲁猪的抗体反应。采用了三种研究设计。首先,我们追踪了用奥芬达唑治疗的患有囊尾蚴病的猪对这两种诊断蛋白的抗体反应动力学。其次,我们测量了初次实验感染猪的抗体反应。第三,我们追踪了患有囊尾蚴病的母猪所生仔猪中针对rGp50和sTs18var1的母源抗体。这些研究表明,FAST-ELISA中针对这两种诊断蛋白的抗体反应与活囊肿感染在数量上相关,其中抗sTs18var1活性对感染状态最敏感。