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Comparison of Recombinant Trypanosoma cruzi Peptide Mixtures versus Multiepitope Chimeric Proteins as Sensitizing Antigens for Immunodiagnosis▿

机译:重组克氏锥虫多肽混合物与多表位嵌合蛋白作为免疫诊断敏感抗原的比较▿

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摘要

The aim of this work was to determine the best strategy to display antigens (Ags) on immunochemical devices to improve test selectivity and sensitivity. We comparatively evaluated five Trypanosoma cruzi antigenic recombinant peptides, chose the three more sensitive ones, built up chimeras bearing these selected Ags, and systematically compared by enzyme-linked immunosorbent assay the performance of the assortments of those peptides with that of the multiepitope constructions bearing all those peptides lineally fused. The better-performing Ags that were compared included peptides homologous to the previously described T. cruzi flagellar repetitive Ag (here named RP1), shed acute-phase Ag (RP2), B13 (RP5), and the chimeric recombinant proteins CP1 and CP2, bearing repetitions of RP1-RP2 and RP1-RP2-RP5, respectively. The diagnostic performances of these Ags were assessed for discrimination efficiency by the formula +OD/cutoff value (where +OD is the mean optical density value of the positive serum samples tested), in comparison with each other either alone, in mixtures, or as peptide-fused chimeras and with total parasite homogenate (TPH). The discrimination efficiency values obtained for CP1 and CP2 were 25% and 52% higher, respectively, than those of their individual-Ag mixtures. CP2 was the only Ag that showed enhanced discrimination efficiency between Chagas' disease-positive and -negative samples, compared with TPH. This study highlights the convenience of performing immunochemical assays using hybrid, single-molecule, chimeric Ags instead of peptide mixtures. CP2 preliminary tests rendered 98.6% sensitivity when evaluated with a 141-Chagas' disease-positive serum sample panel and 99.4% specificity when assessed with a 164-Chagas' disease-negative serum sample panel containing 15 samples from individuals infected with Leishmania spp.
机译:这项工作的目的是确定在免疫化学设备上展示抗原(Ags)的最佳策略,以提高测试的选择性和灵敏度。我们比较评估了五种克氏锥虫抗原性重组肽,选择了三种敏感性更高的肽,构建了带有这些选定Ag的嵌合体,并通过酶联免疫吸附试验系统地比较了这些肽的分类与携带所有肽的多表位构建物的性能。那些肽线性融合。相比之下,性能更好的Ags包括与先前描述的克鲁氏鞭毛鞭毛重复Ag(此处称为RP1)同源的肽,脱落的急性期Ag(RP2),B13(RP5)以及嵌合重组蛋白CP1和CP2,分别重复RP1-RP2和RP1-RP2-RP5。单独,以混合物形式或以混合物形式比较,通过公式+ OD /临界值(其中+ OD是测试的阳性血清样品的平均光密度值),评估了这些Ag的诊断性能。肽融合的嵌合体,并具有总寄生虫匀浆(TPH)。 CP1和CP2的辨别效率值分别比其单独的Ag混合物高25%和52%。与TPH相比,CP2是唯一在Chagas疾病阳性和阴性样品之间显示出更高鉴别效率的Ag。这项研究强调了使用杂交,单分子,嵌合Ags而非肽混合物进行免疫化学分析的便利性。当使用141-Chagas's疾病阳性血清样本组进行评估时,CP2初步测试的灵敏度为98.6%,而使用包含15例来自利什曼原虫属个体的样本的164-Chagas's疾病阴性血清样本组进行评估时,特异性为99.4%。

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