Evaluation of an enzyme-linked immunosorbent assay for the diagnosis of Chagas' disease using synthetic peptides
Author
dc.contributor.author
Vergara Vergara, Geraldine
Author
dc.contributor.author
Veloso,
Author
dc.contributor.author
Gonzalez, R.
Author
dc.contributor.author
Lorca,
Admission date
dc.date.accessioned
2019-01-29T14:52:12Z
Available date
dc.date.available
2019-01-29T14:52:12Z
Publication date
dc.date.issued
1992
Cita de ítem
dc.identifier.citation
American Journal of Tropical Medicine and Hygiene, Volumen 46, Issue 1, 2018, Pages 39-43
Identifier
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00029637
Identifier
dc.identifier.other
10.4269/ajtmh.1992.46.39
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/161037
Abstract
dc.description.abstract
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 > 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.