2007
DOI: 10.1590/s0074-02762007005000084
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Taenia solium metacestode immunodominant peptides recognized by IgG antibodies in cerebrospinal fluid and serum paired samples from patients with active and inactive neurocysticercosis

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Cited by 8 publications
(10 citation statements)
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“…However, the explanation for the specific selection of reactive peptides to NC‐In sera may be derived from results presented elsewhere (41), which demonstrated that active and inactive NC patients sera presented differential protein profiles. The immunodominant bands of 47–52, 64–68 and 70 kDa were predominant when testing the NC‐Ac sera, while the 12‐ to 14‐ and 39‐ to 42‐kDa bands were not recognized by the NC‐In sera.…”
Section: Discussionmentioning
confidence: 99%
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“…However, the explanation for the specific selection of reactive peptides to NC‐In sera may be derived from results presented elsewhere (41), which demonstrated that active and inactive NC patients sera presented differential protein profiles. The immunodominant bands of 47–52, 64–68 and 70 kDa were predominant when testing the NC‐Ac sera, while the 12‐ to 14‐ and 39‐ to 42‐kDa bands were not recognized by the NC‐In sera.…”
Section: Discussionmentioning
confidence: 99%
“…Other studies have also demonstrated the ability to distinguish active from inactive NC forms (13–16,41), suggesting that this is related to differential patterns of antigen’s epitope recognition in the two phases of the disease, and part of this antigenic variations may be attributed to protein conformation and glycosylation (33). In our study, preparation of antigen extracts and chicken immunization may have generated loss of protein conformation or differential protein modifications, and these alterations may have artificially created antigens and specific epitopes that are mainly recognized by patients’ sera with the inactive NC form.…”
Section: Discussionmentioning
confidence: 99%
“…A total saline extract with 50 metacestodes of T. solium was prepared and the obtained extract was divided into aliquots of 200 μL, identified and stored at −20 °C until processing. Serum samples were submitted to the ELISA test in accordance with Barcelos et al 10 Some 200 μg of the total saline extract protein was applied by 10 × 8 cm gel and subjected to 12% polyacrylamide gel electrophoresis (SDS-PAGE) for separation of the peptides present in the antigenic extract and subsequent transfer to 0.45 μm pore size nitrocellulose membranes. After transfer, the nitrocellulose membranes were cut into 3 mm strips.…”
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confidence: 99%
“…The antigenic peptides recognized by IgG antibodies present in the reagent serum samples in the ELISA were analyzed by Western blotting (WB). 10 The criterion for positivity in WB adopted was the recognition of at least two of the peptides, 18, 24, 28–32, 39–42, 47–52, 64–68, and 70 kDa, in WB specific for cysticercosis. 10 The results obtained in the ELISA and WB were analyzed using two-way ANOVA and Fisher's exact tests with p ≤ 0.05 in the software GraphPad Prism version 5.0.…”
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confidence: 99%
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