Scharfstein J, Luquetti A, Murta A C, Senna M, Rezende J M, Rassi A, Mendonça-Previato L
Am J Trop Med Hyg. 1985 Nov;34(6):1153-60. doi: 10.4269/ajtmh.1985.34.1153.
Development of a highly specific test system for the diagnosis of Chagas' disease (CD) was sought using Gp25, a surface glycoprotein recently isolated from Trypanosoma cruzi culture forms. Radioimmunoprecipitation assays were performed to screen 567 sera for IgG antibodies to Gp25. Correct diagnosis was attained in 97.8% of the 321 sera collected from chagasic patients in several endemic areas of South America. Sera from patients with various clinical forms of chronic disease displayed similar levels of antibodies (Abs) to Gp25. Moreover, there was little cross-reactivity when assayed against 246 sera from non-chagasic individuals, including 105 samples from individuals infected with unrelated trypanosomatids. Cross-reactivity was found in two such sera; these were used to identify a minor protein contaminant as the nonspecific antigen. Residual cross-reactive molecules were eliminated from Gp25 by affinity purification on Concanavalin A (Con A) columns. We recommend this antigen-antibody system for use in routine screening of blood donors.
人们试图利用Gp25(一种最近从克氏锥虫培养形式中分离出的表面糖蛋白)开发一种用于诊断恰加斯病(CD)的高特异性检测系统。进行放射免疫沉淀试验以筛选567份血清中针对Gp25的IgG抗体。从南美洲几个流行地区的恰加斯病患者收集的321份血清中,97.8%的血清得到了正确诊断。患有各种临床形式慢性病的患者血清显示出对Gp25的抗体(Abs)水平相似。此外,用246份非恰加斯病个体的血清进行检测时,交叉反应性很低,其中包括105份感染无关锥虫的个体样本。在两份这样的血清中发现了交叉反应性;这些血清被用来鉴定一种微量蛋白质污染物为非特异性抗原。通过在伴刀豆球蛋白A(Con A)柱上进行亲和纯化,从Gp25中去除了残留的交叉反应性分子。我们推荐这种抗原-抗体系统用于献血者的常规筛查。