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Preclinical evaluation of a chemically detoxified pneumolysin as pneumococcal vaccine antigen
The use of protein antigens able to protect against the majority of Streptococcus pneumoniae serotypes is envisaged as stand-alone and/or complement to the current capsular polysaccharide-based pneumococcal vaccines. Pneumolysin (Ply) is a key virulence factor that is highly conserved in amino acid...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5287308/ https://www.ncbi.nlm.nih.gov/pubmed/27768518 http://dx.doi.org/10.1080/21645515.2016.1234553 |
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author | Hermand, Philippe Vandercammen, Annick Mertens, Emmanuel Di Paolo, Emmanuel Verlant, Vincent Denoël, Philippe Godfroid, Fabrice |
author_facet | Hermand, Philippe Vandercammen, Annick Mertens, Emmanuel Di Paolo, Emmanuel Verlant, Vincent Denoël, Philippe Godfroid, Fabrice |
author_sort | Hermand, Philippe |
collection | PubMed |
description | The use of protein antigens able to protect against the majority of Streptococcus pneumoniae serotypes is envisaged as stand-alone and/or complement to the current capsular polysaccharide-based pneumococcal vaccines. Pneumolysin (Ply) is a key virulence factor that is highly conserved in amino acid sesec-typsecquence across pneumococcal serotypes, and therefore may be considered as a vaccine target. However, native Ply cannot be used in vaccines due to its intrinsic cytolytic activity. In the present work a completely, irreversibly detoxified pneumolysin (dPly) has been generated using an optimized formaldehyde treatment. Detoxi-fication was confirmed by dPly challenge in mice and histological analysis of the injection site in rats. Immunization with dPly elicited Ply-specific functional antibodies that were able to inhibit Ply activity in a hemolysis assay. In addition, immunization with dPly protected mice against lethal intranasal challenge with Ply, and intranasal immunization inhibited nasopharyngeal colonization after intranasal challenge with homologous or heterologous pneumococcal strain. Our findings supported dPly as a valid candidate antigen for further pneumococcal vaccine development. |
format | Online Article Text |
id | pubmed-5287308 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-52873082017-02-15 Preclinical evaluation of a chemically detoxified pneumolysin as pneumococcal vaccine antigen Hermand, Philippe Vandercammen, Annick Mertens, Emmanuel Di Paolo, Emmanuel Verlant, Vincent Denoël, Philippe Godfroid, Fabrice Hum Vaccin Immunother Research Paper The use of protein antigens able to protect against the majority of Streptococcus pneumoniae serotypes is envisaged as stand-alone and/or complement to the current capsular polysaccharide-based pneumococcal vaccines. Pneumolysin (Ply) is a key virulence factor that is highly conserved in amino acid sesec-typsecquence across pneumococcal serotypes, and therefore may be considered as a vaccine target. However, native Ply cannot be used in vaccines due to its intrinsic cytolytic activity. In the present work a completely, irreversibly detoxified pneumolysin (dPly) has been generated using an optimized formaldehyde treatment. Detoxi-fication was confirmed by dPly challenge in mice and histological analysis of the injection site in rats. Immunization with dPly elicited Ply-specific functional antibodies that were able to inhibit Ply activity in a hemolysis assay. In addition, immunization with dPly protected mice against lethal intranasal challenge with Ply, and intranasal immunization inhibited nasopharyngeal colonization after intranasal challenge with homologous or heterologous pneumococcal strain. Our findings supported dPly as a valid candidate antigen for further pneumococcal vaccine development. Taylor & Francis 2016-10-21 /pmc/articles/PMC5287308/ /pubmed/27768518 http://dx.doi.org/10.1080/21645515.2016.1234553 Text en © 2017 GSK Biologicals SA. Published with license by Taylor & Francis. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted. |
spellingShingle | Research Paper Hermand, Philippe Vandercammen, Annick Mertens, Emmanuel Di Paolo, Emmanuel Verlant, Vincent Denoël, Philippe Godfroid, Fabrice Preclinical evaluation of a chemically detoxified pneumolysin as pneumococcal vaccine antigen |
title | Preclinical evaluation of a chemically detoxified pneumolysin as pneumococcal vaccine antigen |
title_full | Preclinical evaluation of a chemically detoxified pneumolysin as pneumococcal vaccine antigen |
title_fullStr | Preclinical evaluation of a chemically detoxified pneumolysin as pneumococcal vaccine antigen |
title_full_unstemmed | Preclinical evaluation of a chemically detoxified pneumolysin as pneumococcal vaccine antigen |
title_short | Preclinical evaluation of a chemically detoxified pneumolysin as pneumococcal vaccine antigen |
title_sort | preclinical evaluation of a chemically detoxified pneumolysin as pneumococcal vaccine antigen |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5287308/ https://www.ncbi.nlm.nih.gov/pubmed/27768518 http://dx.doi.org/10.1080/21645515.2016.1234553 |
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