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IL-1 Fragment Modulates Immune Response Elicited by Recombinant Bacillus subtilis Spores Presenting an Antigen/Adjuvant Chimeric Protein
Mucosal immunizations are convenient ways of vaccination, which do not require any trained personnel for administration. One of the major challenges for developing an effective mucosal vaccine is finding appropriate adjuvant. Bacillus subtilis endospores have been shown to help solving these obstacl...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer US
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182635/ https://www.ncbi.nlm.nih.gov/pubmed/30178298 http://dx.doi.org/10.1007/s12033-018-0117-0 |
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author | Potocki, Wojciech Negri, Alessandro Peszyńska-Sularz, Grażyna Hinc, Krzysztof Obuchowski, Michał Iwanicki, Adam |
author_facet | Potocki, Wojciech Negri, Alessandro Peszyńska-Sularz, Grażyna Hinc, Krzysztof Obuchowski, Michał Iwanicki, Adam |
author_sort | Potocki, Wojciech |
collection | PubMed |
description | Mucosal immunizations are convenient ways of vaccination, which do not require any trained personnel for administration. One of the major challenges for developing an effective mucosal vaccine is finding appropriate adjuvant. Bacillus subtilis endospores have been shown to help solving these obstacles while serving as a platform for presentation of both, antigens and adjuvants. In this study, we have successfully designed and constructed recombinant spores displaying an antigen/adjuvant chimeric protein. We have used a fragment of Clostridium difficile flagellar cap FliD protein as antigen and VQGEESNDK peptide, a fragment of human IL-1β, as adjuvant. Recombinant spores presenting FliD were able to elicit immune response in orally immunized mice which could be evaluated by detection of FliD-specific IgA antibodies in feces of immunized animals. Moreover, the presence of IL-1β fragment significantly changed characteristics of elicited immune response. Obtained results show that recombinant spores presenting an antigen/adjuvant chimeric protein exhibit both properties in mucosal immunization of mice. Moreover, IL-1β fragment could serve as valuable adjuvant in B. subtilis spore-based mucosal vaccines. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12033-018-0117-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6182635 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-61826352018-10-24 IL-1 Fragment Modulates Immune Response Elicited by Recombinant Bacillus subtilis Spores Presenting an Antigen/Adjuvant Chimeric Protein Potocki, Wojciech Negri, Alessandro Peszyńska-Sularz, Grażyna Hinc, Krzysztof Obuchowski, Michał Iwanicki, Adam Mol Biotechnol Original Paper Mucosal immunizations are convenient ways of vaccination, which do not require any trained personnel for administration. One of the major challenges for developing an effective mucosal vaccine is finding appropriate adjuvant. Bacillus subtilis endospores have been shown to help solving these obstacles while serving as a platform for presentation of both, antigens and adjuvants. In this study, we have successfully designed and constructed recombinant spores displaying an antigen/adjuvant chimeric protein. We have used a fragment of Clostridium difficile flagellar cap FliD protein as antigen and VQGEESNDK peptide, a fragment of human IL-1β, as adjuvant. Recombinant spores presenting FliD were able to elicit immune response in orally immunized mice which could be evaluated by detection of FliD-specific IgA antibodies in feces of immunized animals. Moreover, the presence of IL-1β fragment significantly changed characteristics of elicited immune response. Obtained results show that recombinant spores presenting an antigen/adjuvant chimeric protein exhibit both properties in mucosal immunization of mice. Moreover, IL-1β fragment could serve as valuable adjuvant in B. subtilis spore-based mucosal vaccines. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12033-018-0117-0) contains supplementary material, which is available to authorized users. Springer US 2018-09-03 2018 /pmc/articles/PMC6182635/ /pubmed/30178298 http://dx.doi.org/10.1007/s12033-018-0117-0 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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. |
spellingShingle | Original Paper Potocki, Wojciech Negri, Alessandro Peszyńska-Sularz, Grażyna Hinc, Krzysztof Obuchowski, Michał Iwanicki, Adam IL-1 Fragment Modulates Immune Response Elicited by Recombinant Bacillus subtilis Spores Presenting an Antigen/Adjuvant Chimeric Protein |
title | IL-1 Fragment Modulates Immune Response Elicited by Recombinant Bacillus subtilis Spores Presenting an Antigen/Adjuvant Chimeric Protein |
title_full | IL-1 Fragment Modulates Immune Response Elicited by Recombinant Bacillus subtilis Spores Presenting an Antigen/Adjuvant Chimeric Protein |
title_fullStr | IL-1 Fragment Modulates Immune Response Elicited by Recombinant Bacillus subtilis Spores Presenting an Antigen/Adjuvant Chimeric Protein |
title_full_unstemmed | IL-1 Fragment Modulates Immune Response Elicited by Recombinant Bacillus subtilis Spores Presenting an Antigen/Adjuvant Chimeric Protein |
title_short | IL-1 Fragment Modulates Immune Response Elicited by Recombinant Bacillus subtilis Spores Presenting an Antigen/Adjuvant Chimeric Protein |
title_sort | il-1 fragment modulates immune response elicited by recombinant bacillus subtilis spores presenting an antigen/adjuvant chimeric protein |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182635/ https://www.ncbi.nlm.nih.gov/pubmed/30178298 http://dx.doi.org/10.1007/s12033-018-0117-0 |
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