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A Novel Vaccine Approach for Chagas Disease Using Rare Adenovirus Serotype 48 Vectors
Due to the increasing amount of people afflicted worldwide with Chagas disease and an increasing prevalence in the United States, there is a greater need to develop a safe and effective vaccine for this neglected disease. Adenovirus serotype 5 (Ad5) is the most common adenovirus vector used for gene...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4810268/ https://www.ncbi.nlm.nih.gov/pubmed/26978385 http://dx.doi.org/10.3390/v8030078 |
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author | Farrow, Anitra L. Peng, Binghao J. Gu, Linlin Krendelchtchikov, Alexandre Matthews, Qiana L. |
author_facet | Farrow, Anitra L. Peng, Binghao J. Gu, Linlin Krendelchtchikov, Alexandre Matthews, Qiana L. |
author_sort | Farrow, Anitra L. |
collection | PubMed |
description | Due to the increasing amount of people afflicted worldwide with Chagas disease and an increasing prevalence in the United States, there is a greater need to develop a safe and effective vaccine for this neglected disease. Adenovirus serotype 5 (Ad5) is the most common adenovirus vector used for gene therapy and vaccine approaches, but its efficacy is limited by preexisting vector immunity in humans resulting from natural infections. Therefore, we have employed rare serotype adenovirus 48 (Ad48) as an alternative choice for adenovirus/Chagas vaccine therapy. In this study, we modified Ad5 and Ad48 vectors to contain T. cruzi’s amastigote surface protein 2 (ASP-2) in the adenoviral early gene. We also modified Ad5 and Ad48 vectors to utilize the “Antigen Capsid-Incorporation” strategy by adding T. cruzi epitopes to protein IX (pIX). Mice that were immunized with the modified vectors were able to elicit T. cruzi-specific humoral and cellular responses. This study indicates that Ad48-modified vectors function comparable to or even premium to Ad5-modified vectors. This study provides novel data demonstrating that Ad48 can be used as a potential adenovirus vaccine vector against Chagas disease. |
format | Online Article Text |
id | pubmed-4810268 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-48102682016-04-04 A Novel Vaccine Approach for Chagas Disease Using Rare Adenovirus Serotype 48 Vectors Farrow, Anitra L. Peng, Binghao J. Gu, Linlin Krendelchtchikov, Alexandre Matthews, Qiana L. Viruses Article Due to the increasing amount of people afflicted worldwide with Chagas disease and an increasing prevalence in the United States, there is a greater need to develop a safe and effective vaccine for this neglected disease. Adenovirus serotype 5 (Ad5) is the most common adenovirus vector used for gene therapy and vaccine approaches, but its efficacy is limited by preexisting vector immunity in humans resulting from natural infections. Therefore, we have employed rare serotype adenovirus 48 (Ad48) as an alternative choice for adenovirus/Chagas vaccine therapy. In this study, we modified Ad5 and Ad48 vectors to contain T. cruzi’s amastigote surface protein 2 (ASP-2) in the adenoviral early gene. We also modified Ad5 and Ad48 vectors to utilize the “Antigen Capsid-Incorporation” strategy by adding T. cruzi epitopes to protein IX (pIX). Mice that were immunized with the modified vectors were able to elicit T. cruzi-specific humoral and cellular responses. This study indicates that Ad48-modified vectors function comparable to or even premium to Ad5-modified vectors. This study provides novel data demonstrating that Ad48 can be used as a potential adenovirus vaccine vector against Chagas disease. MDPI 2016-03-10 /pmc/articles/PMC4810268/ /pubmed/26978385 http://dx.doi.org/10.3390/v8030078 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Farrow, Anitra L. Peng, Binghao J. Gu, Linlin Krendelchtchikov, Alexandre Matthews, Qiana L. A Novel Vaccine Approach for Chagas Disease Using Rare Adenovirus Serotype 48 Vectors |
title | A Novel Vaccine Approach for Chagas Disease Using Rare Adenovirus Serotype 48 Vectors |
title_full | A Novel Vaccine Approach for Chagas Disease Using Rare Adenovirus Serotype 48 Vectors |
title_fullStr | A Novel Vaccine Approach for Chagas Disease Using Rare Adenovirus Serotype 48 Vectors |
title_full_unstemmed | A Novel Vaccine Approach for Chagas Disease Using Rare Adenovirus Serotype 48 Vectors |
title_short | A Novel Vaccine Approach for Chagas Disease Using Rare Adenovirus Serotype 48 Vectors |
title_sort | novel vaccine approach for chagas disease using rare adenovirus serotype 48 vectors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4810268/ https://www.ncbi.nlm.nih.gov/pubmed/26978385 http://dx.doi.org/10.3390/v8030078 |
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