Vergara U, Veloso C, Gonzalez A, Lorca M
Departamento de Ciencas Biologicas y de Preclinicos, Facultad de Medicina, Universidad de Chile, Santiago.
Am J Trop Med Hyg. 1992 Jan;46(1):39-43. doi: 10.4269/ajtmh.1992.46.39.
An enzyme-linked immunosorbent assay (ELISA) has been developed to detect antibodies in human sera to synthetic peptides derived from the repeating amino acid sequence in recombinant Trypanosoma cruzi antigens. Sixty serum samples from patients with chronic Chagas' disease were used to determine the reactivity against the synthetic repeat peptides derived from clones 1, 2, 30, 36, and shed acute phase antigen (SAPA). Ninety-eight percent of the samples had detectable antibodies to one or more of the synthetic peptides at titers greater than 1:100. The percentage of reactive sera increased from 28% with peptide SAPA to 93% with peptide 2. The exposure of patients to T. cruzi was reflected in indirect immunofluorescent antibody titers to fixed epimastigotes. Comparisons between ELISA and immunoradiometric assay data indicated that both tests were of approximately equal sensitivity.
已开发出一种酶联免疫吸附测定(ELISA)法,用于检测人血清中针对重组克氏锥虫抗原重复氨基酸序列衍生的合成肽的抗体。使用60份慢性恰加斯病患者的血清样本,来确定其对来自克隆1、2、30、36的合成重复肽以及急性期释放抗原(SAPA)的反应性。98%的样本在滴度大于1:100时可检测到针对一种或多种合成肽的抗体。反应血清的百分比从针对肽SAPA的28%增至针对肽2的93%。患者对克氏锥虫的暴露情况通过对固定后鞭毛体的间接免疫荧光抗体滴度反映出来。ELISA和免疫放射测定数据的比较表明,两种检测方法的灵敏度大致相同。