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Immunocontraception: Filamentous Bacteriophage as a Platform for Vaccine Development

BACKGROUND: Population control of domestic, wild, invasive, and captive animal species is a global issue of importance to public health, animal welfare and the economy. There is pressing need for effective, safe, and inexpensive contraceptive technologies to ad-dress this problem. Contraceptive vacc...

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Autores principales: Samoylova, Tatiana I., Braden, Timothy D., Spencer, Jennifer A., Bartol, Frank F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5738698/
https://www.ncbi.nlm.nih.gov/pubmed/28901276
http://dx.doi.org/10.2174/0929867324666170911160426
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author Samoylova, Tatiana I.
Braden, Timothy D.
Spencer, Jennifer A.
Bartol, Frank F.
author_facet Samoylova, Tatiana I.
Braden, Timothy D.
Spencer, Jennifer A.
Bartol, Frank F.
author_sort Samoylova, Tatiana I.
collection PubMed
description BACKGROUND: Population control of domestic, wild, invasive, and captive animal species is a global issue of importance to public health, animal welfare and the economy. There is pressing need for effective, safe, and inexpensive contraceptive technologies to ad-dress this problem. Contraceptive vaccines, designed to stimulate the immune system in order to block critical reproductive events and suppress fertility, may provide a solution. Fil-amentous bacteriophages can be used as platforms for development of such vaccines. OBJECTIVE: In this review authors highlight structural and immunogenic properties of fila-mentous phages, and discuss applications of phage-peptide vaccines for advancement of immunocontraception technology in animals. RESULTS: Phages can be engineered to display fusion (non-phage) peptides as coat proteins. Such modifications can be accomplished via genetic manipulation of phage DNA, or by chemical conjugation of synthetic peptides to phage surface proteins. Phage fusions with antigenic determinants induce humoral as well as cell-mediated immune responses in ani-mals, making them attractive as vaccines. Additional advantages of the phage platform include environmental stability, low cost, and safety for immunized animals and those ad-ministering the vaccines. CONCLUSION: Filamentous phages are viable platforms for vaccine development that can be engineered with molecular and organismal specificity. Phage-based vaccines can be pro-duced in abundance at low cost, are environmentally stable, and are immunogenic when administered via multiple routes. These features are essential for a contraceptive vaccine to be operationally practical in animal applications. Adaptability of the phage platform also makes it attractive for design of human immunocontraceptive agents.
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spelling pubmed-57386982017-12-29 Immunocontraception: Filamentous Bacteriophage as a Platform for Vaccine Development Samoylova, Tatiana I. Braden, Timothy D. Spencer, Jennifer A. Bartol, Frank F. Curr Med Chem Article BACKGROUND: Population control of domestic, wild, invasive, and captive animal species is a global issue of importance to public health, animal welfare and the economy. There is pressing need for effective, safe, and inexpensive contraceptive technologies to ad-dress this problem. Contraceptive vaccines, designed to stimulate the immune system in order to block critical reproductive events and suppress fertility, may provide a solution. Fil-amentous bacteriophages can be used as platforms for development of such vaccines. OBJECTIVE: In this review authors highlight structural and immunogenic properties of fila-mentous phages, and discuss applications of phage-peptide vaccines for advancement of immunocontraception technology in animals. RESULTS: Phages can be engineered to display fusion (non-phage) peptides as coat proteins. Such modifications can be accomplished via genetic manipulation of phage DNA, or by chemical conjugation of synthetic peptides to phage surface proteins. Phage fusions with antigenic determinants induce humoral as well as cell-mediated immune responses in ani-mals, making them attractive as vaccines. Additional advantages of the phage platform include environmental stability, low cost, and safety for immunized animals and those ad-ministering the vaccines. CONCLUSION: Filamentous phages are viable platforms for vaccine development that can be engineered with molecular and organismal specificity. Phage-based vaccines can be pro-duced in abundance at low cost, are environmentally stable, and are immunogenic when administered via multiple routes. These features are essential for a contraceptive vaccine to be operationally practical in animal applications. Adaptability of the phage platform also makes it attractive for design of human immunocontraceptive agents. Bentham Science Publishers 2017-10 2017-10 /pmc/articles/PMC5738698/ /pubmed/28901276 http://dx.doi.org/10.2174/0929867324666170911160426 Text en © 2017 Bentham Science Publishers https://creativecommons.org/licenses/by-nc/4.0/legalcode This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/legalcode), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Samoylova, Tatiana I.
Braden, Timothy D.
Spencer, Jennifer A.
Bartol, Frank F.
Immunocontraception: Filamentous Bacteriophage as a Platform for Vaccine Development
title Immunocontraception: Filamentous Bacteriophage as a Platform for Vaccine Development
title_full Immunocontraception: Filamentous Bacteriophage as a Platform for Vaccine Development
title_fullStr Immunocontraception: Filamentous Bacteriophage as a Platform for Vaccine Development
title_full_unstemmed Immunocontraception: Filamentous Bacteriophage as a Platform for Vaccine Development
title_short Immunocontraception: Filamentous Bacteriophage as a Platform for Vaccine Development
title_sort immunocontraception: filamentous bacteriophage as a platform for vaccine development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5738698/
https://www.ncbi.nlm.nih.gov/pubmed/28901276
http://dx.doi.org/10.2174/0929867324666170911160426
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