Title |
Immunoinformatics prediction of linear epitopes from Taenia solium TSOL18 |
Authors |
Mirko Zimic1*, Andres Hazaet Gutierrez1, Robert Hugh Gilman2, 3, Cesar Lopez1, Miguel Quiliano1, Wilfredo Evangelista1, Armando Gonzales4, Hector Hugo Garcia2, 5, Patricia Sheen2 |
Affiliation |
1Unidad de Bioinformatica. Laboratorios de Investigacion y Desarrollo, Facultad de Ciencias y Filosofia, Universidad Peruana Cayetano Heredia; 2Laboratorio de Enfermedades Infecciosas. Laboratorios de Investigacion y Desarrollo, Facultad de Ciencias y Filosofia, Universidad Peruana Cayetano Heredia; 3Department of International Health. Bloomberg School of Public Health, Johns Hopkins University; 4Facultad de Veterinaria, Universidad Nacional Mayor de San Marcos, Peru; 5Cysticercosis Unit, Instituto de Ciencias Neurologicas, Peru
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mzimic@jhsph.edu; *Corresponding author
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Phone |
(511) 483-2942
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Fax |
(511) 483-2942
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Article Type |
Hypothesis
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Date |
Received June 02, 2011; Accepted June 03, 2011; Published June 23, 2011
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Abstract |
Cysticercosis is a public health problem in several developing countries. The oncosphere protein TSOL18 is the most immunogenic and protective antigen ever reported against porcine cysticercosis, although no specific epitope has been identified to account for these properties. Recent evidence suggests that protection might be associated with conformational epitopes. Linear epitopes from TSOL18 were computationally predicted and evaluated for immunogenicity and protection against porcine cysticercosis. A synthetic peptide was designed based on predicted linear B cell and T cell epitopes that are exposed on the surface of the theoretically modeled structure of TSOL18. Three surface epitopes from TSOL18 were predicted as immunogenic. A peptide comprising a linear arrangement of these epitopes was chemically synthesized. The capacity of the synthetic peptide to protect pigs against an oral challenge with Taenia solium proglottids was tested in a vaccine trial. The synthetic peptide was able to produce IgG antibodies in pigs and was associated to a reduction of the number of cysts, although was not able to provide complete protection, defined as the complete absence of cysts in necropsy. This study demonstrated that B cell and T cell predicted epitopes from TSOL18 were not able to completely protect pigs against an oral challenge with Taenia solium proglottids. Therefore, other linear epitopes or eventually conformational epitopes may be responsible for the protection conferred by TSOL18.
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Citation |
Zimic et al.
Bioinformation 6(7): 271-274 (2011) |
Edited by |
P Kangueane
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ISSN |
0973-2063
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Publisher |
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License |
This is an Open Access article which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. This is distributed under the terms of the Creative Commons Attribution License. |