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PilVax – a novel peptide delivery platform for the development of mucosal vaccines
Peptide vaccines are an attractive strategy to engineer the induction of highly targeted immune responses and avoid potentially allergenic and/or reactogenic protein regions. However, peptides by themselves are often unstable and poorly immunogenic, necessitating the need for an adjuvant and a speci...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5803258/ https://www.ncbi.nlm.nih.gov/pubmed/29416095 http://dx.doi.org/10.1038/s41598-018-20863-7 |
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author | Wagachchi, Dasun Tsai, Jia-Yun C. Chalmers, Callum Blanchett, Sam Loh, Jacelyn M. S. Proft, Thomas |
author_facet | Wagachchi, Dasun Tsai, Jia-Yun C. Chalmers, Callum Blanchett, Sam Loh, Jacelyn M. S. Proft, Thomas |
author_sort | Wagachchi, Dasun |
collection | PubMed |
description | Peptide vaccines are an attractive strategy to engineer the induction of highly targeted immune responses and avoid potentially allergenic and/or reactogenic protein regions. However, peptides by themselves are often unstable and poorly immunogenic, necessitating the need for an adjuvant and a specialised delivery system. We have developed a novel peptide delivery platform (PilVax) that allows the presentation of a stabilised and highly amplified peptide as part of the group A streptococcus serotype M1 pilus structure (PilM1) on the surface of the non-pathogenic bacterium Lactococcus lactis. To show proof of concept, we have successfully inserted the model peptide Ova(324–339) into 3 different loop regions of the backbone protein Spy0128, which resulted in the assembly of the pilus containing large numbers of peptide on the surface of L. lactis. Intranasal immunisation of mice with L. lactis PilM1-Ova generated measurable Ova-specific systemic and mucosal responses (IgA and IgG). Furthermore, we show that multiple peptides can be inserted into the PilVax platform and that peptides can also be incorporated into structurally similar, but antigenically different pilus structures. PilVax may be useful as a cost-effective platform for the development of peptide vaccines against a variety of important human pathogens. |
format | Online Article Text |
id | pubmed-5803258 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58032582018-02-14 PilVax – a novel peptide delivery platform for the development of mucosal vaccines Wagachchi, Dasun Tsai, Jia-Yun C. Chalmers, Callum Blanchett, Sam Loh, Jacelyn M. S. Proft, Thomas Sci Rep Article Peptide vaccines are an attractive strategy to engineer the induction of highly targeted immune responses and avoid potentially allergenic and/or reactogenic protein regions. However, peptides by themselves are often unstable and poorly immunogenic, necessitating the need for an adjuvant and a specialised delivery system. We have developed a novel peptide delivery platform (PilVax) that allows the presentation of a stabilised and highly amplified peptide as part of the group A streptococcus serotype M1 pilus structure (PilM1) on the surface of the non-pathogenic bacterium Lactococcus lactis. To show proof of concept, we have successfully inserted the model peptide Ova(324–339) into 3 different loop regions of the backbone protein Spy0128, which resulted in the assembly of the pilus containing large numbers of peptide on the surface of L. lactis. Intranasal immunisation of mice with L. lactis PilM1-Ova generated measurable Ova-specific systemic and mucosal responses (IgA and IgG). Furthermore, we show that multiple peptides can be inserted into the PilVax platform and that peptides can also be incorporated into structurally similar, but antigenically different pilus structures. PilVax may be useful as a cost-effective platform for the development of peptide vaccines against a variety of important human pathogens. Nature Publishing Group UK 2018-02-07 /pmc/articles/PMC5803258/ /pubmed/29416095 http://dx.doi.org/10.1038/s41598-018-20863-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wagachchi, Dasun Tsai, Jia-Yun C. Chalmers, Callum Blanchett, Sam Loh, Jacelyn M. S. Proft, Thomas PilVax – a novel peptide delivery platform for the development of mucosal vaccines |
title | PilVax – a novel peptide delivery platform for the development of mucosal vaccines |
title_full | PilVax – a novel peptide delivery platform for the development of mucosal vaccines |
title_fullStr | PilVax – a novel peptide delivery platform for the development of mucosal vaccines |
title_full_unstemmed | PilVax – a novel peptide delivery platform for the development of mucosal vaccines |
title_short | PilVax – a novel peptide delivery platform for the development of mucosal vaccines |
title_sort | pilvax – a novel peptide delivery platform for the development of mucosal vaccines |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5803258/ https://www.ncbi.nlm.nih.gov/pubmed/29416095 http://dx.doi.org/10.1038/s41598-018-20863-7 |
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