Title
Immunodiagnosis of human neurocysticercosis using a synthetic peptide selected by phage-display
Date Issued
01 January 2009
Access level
metadata only access
Resource Type
journal article
Author(s)
Hell R.C.R.
Amim P.
de Andrade H.M.
de Avila R.A.M.
Felicori L.
Oliveira A.G.
Oliveira C.A.
Nascimento E.
Tavares C.A.P.
Granier C.
Universidad Federal de Minas Gerais
Abstract
The usefulness of a synthetic peptide in the serodiagnosis of Taenia solium human neurocysticercosis (NC) has been evaluated. Phage-displayed peptides were screened with human antibodies to scolex protein antigen from cysticercus cellulosae (SPACc). One clone was found to interact specifically with anti-SPACc IgGs. The corresponding synthetic peptide was found to be recognized in ELISA by NC patient's sera. The study was carried out with sera from 28 confirmed NC patients, 13 control sera and 73 sera from patients suffering from other infectious diseases. A 93% sensibility and a 94.3% specificity was achieved. Figures of 89% and 31.4% of sensibility and specificity were obtained in a SPACc-based ELISA. Immunoblotting of SPACc with anti-peptide antibodies revealed a single band of ∼ 45 kDa in 1D and four 45 kDa isoforms in 2D-gel electrophoresis. A strong and specific immunostaining in the fibers beneath the suckers, at the base of the rostellum, and in the tissue surrounding the scolex of cysticerci was observed by immunomicroscopy. Our results show that a peptide-based immunodiagnostic of neurocisticercosis can be envisioned. © 2008 Elsevier Inc. All rights reserved.
Start page
129
End page
138
Volume
131
Issue
1
Language
English
OCDE Knowledge area
Inmunología
Scopus EID
2-s2.0-85042592010
PubMed ID
Source
Clinical Immunology
ISSN of the container
15216616
Sponsor(s)
Funding text This work was supported by Fundacão de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG), Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) and carried out within the frame of an exchange program funded by the Institut National de la Santé et de la Recherche Médicale (INSERM, France) and CNPq, Brasil. The authors wish to thank the Biomolecules Group of Federal University of Minas Gerais, Brazil for mass spectrometry analysis. We thank Dr. J. Scott for the gift of phage libraries.
Sources of information: Directorio de Producción Científica Scopus