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Recombinant Enolase of Trypanosoma cruzi as a Novel Vaccine Candidate against Chagas Disease in a Mouse Model of Acute Infection

Trypanosoma cruzi is the protozoan parasite that causes Chagas disease, which is considered by the World Health Organization to be a neglected tropical disease. Two drugs exist for the treatment of Chagas disease, nifurtimox and benznidazole; they are only effective in the acute phase, and a vaccine...

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Autores principales: Arce-Fonseca, Minerva, González-Vázquez, María Cristina, Rodríguez-Morales, Olivia, Graullera-Rivera, Verónica, Aranda-Fraustro, Alberto, Reyes, Pedro A., Carabarin-Lima, Alejandro, Rosales-Encina, José Luis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5964559/
https://www.ncbi.nlm.nih.gov/pubmed/29854848
http://dx.doi.org/10.1155/2018/8964085
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author Arce-Fonseca, Minerva
González-Vázquez, María Cristina
Rodríguez-Morales, Olivia
Graullera-Rivera, Verónica
Aranda-Fraustro, Alberto
Reyes, Pedro A.
Carabarin-Lima, Alejandro
Rosales-Encina, José Luis
author_facet Arce-Fonseca, Minerva
González-Vázquez, María Cristina
Rodríguez-Morales, Olivia
Graullera-Rivera, Verónica
Aranda-Fraustro, Alberto
Reyes, Pedro A.
Carabarin-Lima, Alejandro
Rosales-Encina, José Luis
author_sort Arce-Fonseca, Minerva
collection PubMed
description Trypanosoma cruzi is the protozoan parasite that causes Chagas disease, which is considered by the World Health Organization to be a neglected tropical disease. Two drugs exist for the treatment of Chagas disease, nifurtimox and benznidazole; they are only effective in the acute phase, and a vaccine is currently not available. In this study, we used the recombinant enolase from T. cruzi H8 strain (MHOM/MX/1992/H8 Yucatán) (rTcENO) and its encoding DNA (pBKTcENO) to immunize mice and evaluate their protective effects in an experimental murine model of acute phase infection. Our results showed that mice vaccinated with rTcENO or its encoding DNA were able to generate typical specific antibodies (IgG1, IgG2a, and IgG2b), suggesting that a mixed Th1/Th2 immune response was induced. The parasite burden in the blood was reduced to 69.8% and 71% in mice vaccinated with rTcENO and pBKTcENO, respectively. The group vaccinated with rTcENO achieved 75% survival, in contrast to the group vaccinated with pBKTcENO that showed no survival in comparison to the control groups. Moreover, rTcENO immunization elevated the production of IFN-γ and IL-2 after the parasite challenge, suggesting that the Th1-type immune response was polarized. These results indicated that rTcENO could be used as a vaccine against Chagas disease.
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spelling pubmed-59645592018-05-31 Recombinant Enolase of Trypanosoma cruzi as a Novel Vaccine Candidate against Chagas Disease in a Mouse Model of Acute Infection Arce-Fonseca, Minerva González-Vázquez, María Cristina Rodríguez-Morales, Olivia Graullera-Rivera, Verónica Aranda-Fraustro, Alberto Reyes, Pedro A. Carabarin-Lima, Alejandro Rosales-Encina, José Luis J Immunol Res Research Article Trypanosoma cruzi is the protozoan parasite that causes Chagas disease, which is considered by the World Health Organization to be a neglected tropical disease. Two drugs exist for the treatment of Chagas disease, nifurtimox and benznidazole; they are only effective in the acute phase, and a vaccine is currently not available. In this study, we used the recombinant enolase from T. cruzi H8 strain (MHOM/MX/1992/H8 Yucatán) (rTcENO) and its encoding DNA (pBKTcENO) to immunize mice and evaluate their protective effects in an experimental murine model of acute phase infection. Our results showed that mice vaccinated with rTcENO or its encoding DNA were able to generate typical specific antibodies (IgG1, IgG2a, and IgG2b), suggesting that a mixed Th1/Th2 immune response was induced. The parasite burden in the blood was reduced to 69.8% and 71% in mice vaccinated with rTcENO and pBKTcENO, respectively. The group vaccinated with rTcENO achieved 75% survival, in contrast to the group vaccinated with pBKTcENO that showed no survival in comparison to the control groups. Moreover, rTcENO immunization elevated the production of IFN-γ and IL-2 after the parasite challenge, suggesting that the Th1-type immune response was polarized. These results indicated that rTcENO could be used as a vaccine against Chagas disease. Hindawi 2018-05-07 /pmc/articles/PMC5964559/ /pubmed/29854848 http://dx.doi.org/10.1155/2018/8964085 Text en Copyright © 2018 Minerva Arce-Fonseca et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Arce-Fonseca, Minerva
González-Vázquez, María Cristina
Rodríguez-Morales, Olivia
Graullera-Rivera, Verónica
Aranda-Fraustro, Alberto
Reyes, Pedro A.
Carabarin-Lima, Alejandro
Rosales-Encina, José Luis
Recombinant Enolase of Trypanosoma cruzi as a Novel Vaccine Candidate against Chagas Disease in a Mouse Model of Acute Infection
title Recombinant Enolase of Trypanosoma cruzi as a Novel Vaccine Candidate against Chagas Disease in a Mouse Model of Acute Infection
title_full Recombinant Enolase of Trypanosoma cruzi as a Novel Vaccine Candidate against Chagas Disease in a Mouse Model of Acute Infection
title_fullStr Recombinant Enolase of Trypanosoma cruzi as a Novel Vaccine Candidate against Chagas Disease in a Mouse Model of Acute Infection
title_full_unstemmed Recombinant Enolase of Trypanosoma cruzi as a Novel Vaccine Candidate against Chagas Disease in a Mouse Model of Acute Infection
title_short Recombinant Enolase of Trypanosoma cruzi as a Novel Vaccine Candidate against Chagas Disease in a Mouse Model of Acute Infection
title_sort recombinant enolase of trypanosoma cruzi as a novel vaccine candidate against chagas disease in a mouse model of acute infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5964559/
https://www.ncbi.nlm.nih.gov/pubmed/29854848
http://dx.doi.org/10.1155/2018/8964085
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