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Protection against Experimental Melioidosis following Immunisation with a Lipopolysaccharide-Protein Conjugate
Melioidosis is a severe infectious disease caused by Burkholderia pseudomallei. It is refractory to antibiotic treatment and there is currently no licensed vaccine. In this report we detail the construction and protective efficacy of a polysaccharide-protein conjugate composed of B. pseudomallei lip...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4033506/ https://www.ncbi.nlm.nih.gov/pubmed/24892035 http://dx.doi.org/10.1155/2014/392170 |
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author | Scott, Andrew E. Ngugi, Sarah A. Laws, Thomas R. Corser, David Lonsdale, Claire L. D'Elia, Riccardo V. Titball, Richard W. Williamson, E. Diane Atkins, Timothy P. Prior, Joann L. |
author_facet | Scott, Andrew E. Ngugi, Sarah A. Laws, Thomas R. Corser, David Lonsdale, Claire L. D'Elia, Riccardo V. Titball, Richard W. Williamson, E. Diane Atkins, Timothy P. Prior, Joann L. |
author_sort | Scott, Andrew E. |
collection | PubMed |
description | Melioidosis is a severe infectious disease caused by Burkholderia pseudomallei. It is refractory to antibiotic treatment and there is currently no licensed vaccine. In this report we detail the construction and protective efficacy of a polysaccharide-protein conjugate composed of B. pseudomallei lipopolysaccharide and the H(c) fragment of tetanus toxin. Immunisation of mice with the lipopolysaccharide-conjugate led to significantly reduced bacterial burdens in the spleen 48 hours after challenge and afforded significant protection against a lethal challenge with B. pseudomallei. The conjugate generated significantly higher levels of antigen-specific IgG1 and IgG2a than in lipopolysaccharide-immunised mice. Immunisation with the conjugate also demonstrated a bias towards Th1 type responses, evidenced by high levels of IgG2a. In contrast, immunisation with unconjugated lipopolysaccharide evoked almost no IgG2a demonstrating a bias towards Th2 type responses. This study demonstrates the effectiveness of this approach in the development of an efficacious and protective vaccine against melioidosis. |
format | Online Article Text |
id | pubmed-4033506 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-40335062014-06-02 Protection against Experimental Melioidosis following Immunisation with a Lipopolysaccharide-Protein Conjugate Scott, Andrew E. Ngugi, Sarah A. Laws, Thomas R. Corser, David Lonsdale, Claire L. D'Elia, Riccardo V. Titball, Richard W. Williamson, E. Diane Atkins, Timothy P. Prior, Joann L. J Immunol Res Research Article Melioidosis is a severe infectious disease caused by Burkholderia pseudomallei. It is refractory to antibiotic treatment and there is currently no licensed vaccine. In this report we detail the construction and protective efficacy of a polysaccharide-protein conjugate composed of B. pseudomallei lipopolysaccharide and the H(c) fragment of tetanus toxin. Immunisation of mice with the lipopolysaccharide-conjugate led to significantly reduced bacterial burdens in the spleen 48 hours after challenge and afforded significant protection against a lethal challenge with B. pseudomallei. The conjugate generated significantly higher levels of antigen-specific IgG1 and IgG2a than in lipopolysaccharide-immunised mice. Immunisation with the conjugate also demonstrated a bias towards Th1 type responses, evidenced by high levels of IgG2a. In contrast, immunisation with unconjugated lipopolysaccharide evoked almost no IgG2a demonstrating a bias towards Th2 type responses. This study demonstrates the effectiveness of this approach in the development of an efficacious and protective vaccine against melioidosis. Hindawi Publishing Corporation 2014 2014-05-07 /pmc/articles/PMC4033506/ /pubmed/24892035 http://dx.doi.org/10.1155/2014/392170 Text en Copyright © 2014 Andrew E. Scott et al. https://creativecommons.org/licenses/by/3.0/ 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 Scott, Andrew E. Ngugi, Sarah A. Laws, Thomas R. Corser, David Lonsdale, Claire L. D'Elia, Riccardo V. Titball, Richard W. Williamson, E. Diane Atkins, Timothy P. Prior, Joann L. Protection against Experimental Melioidosis following Immunisation with a Lipopolysaccharide-Protein Conjugate |
title | Protection against Experimental Melioidosis following Immunisation with a Lipopolysaccharide-Protein Conjugate |
title_full | Protection against Experimental Melioidosis following Immunisation with a Lipopolysaccharide-Protein Conjugate |
title_fullStr | Protection against Experimental Melioidosis following Immunisation with a Lipopolysaccharide-Protein Conjugate |
title_full_unstemmed | Protection against Experimental Melioidosis following Immunisation with a Lipopolysaccharide-Protein Conjugate |
title_short | Protection against Experimental Melioidosis following Immunisation with a Lipopolysaccharide-Protein Conjugate |
title_sort | protection against experimental melioidosis following immunisation with a lipopolysaccharide-protein conjugate |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4033506/ https://www.ncbi.nlm.nih.gov/pubmed/24892035 http://dx.doi.org/10.1155/2014/392170 |
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