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GMMA as an Alternative Carrier for a Glycoconjugate Vaccine against Group A Streptococcus
Group A Streptococcus (GAS) causes about 500,000 annual deaths globally, and no vaccines are currently available. The Group A Carbohydrate (GAC), conserved across all GAS serotypes, conjugated to an appropriate carrier protein, represents a promising vaccine candidate. Here, we explored the possibil...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9324507/ https://www.ncbi.nlm.nih.gov/pubmed/35891202 http://dx.doi.org/10.3390/vaccines10071034 |
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author | Palmieri, Elena Kis, Zoltán Ozanne, James Di Benedetto, Roberta Ricchetti, Beatrice Massai, Luisa Carducci, Martina Oldrini, Davide Gasperini, Gianmarco Aruta, Maria Grazia Rossi, Omar Kontoravdi, Cleo Shah, Nilay Mawas, Fatme Micoli, Francesca |
author_facet | Palmieri, Elena Kis, Zoltán Ozanne, James Di Benedetto, Roberta Ricchetti, Beatrice Massai, Luisa Carducci, Martina Oldrini, Davide Gasperini, Gianmarco Aruta, Maria Grazia Rossi, Omar Kontoravdi, Cleo Shah, Nilay Mawas, Fatme Micoli, Francesca |
author_sort | Palmieri, Elena |
collection | PubMed |
description | Group A Streptococcus (GAS) causes about 500,000 annual deaths globally, and no vaccines are currently available. The Group A Carbohydrate (GAC), conserved across all GAS serotypes, conjugated to an appropriate carrier protein, represents a promising vaccine candidate. Here, we explored the possibility to use Generalized Modules for Membrane Antigens (GMMA) as an alternative carrier system for GAC, exploiting their intrinsic adjuvant properties. Immunogenicity of GAC-GMMA conjugate was evaluated in different animal species in comparison to GAC-CRM(197); and the two conjugates were also compared from a techno-economic point of view. GMMA proved to be a good alternative carrier for GAC, resulting in a higher immune response compared to CRM(197) in different mice strains, as verified by ELISA and FACS analyses. Differently from CRM(197), GMMA induced significant levels of anti-GAC IgG titers in mice also in the absence of Alhydrogel. In rabbits, a difference in the immune response could not be appreciated; however, antibodies from GAC-GMMA-immunized animals showed higher affinity toward purified GAC antigen compared to those elicited by GAC-CRM(197). In addition, the GAC-GMMA production process proved to be more cost-effective, making this conjugate particularly attractive for low- and middle-income countries, where this pathogen has a huge burden. |
format | Online Article Text |
id | pubmed-9324507 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-93245072022-07-27 GMMA as an Alternative Carrier for a Glycoconjugate Vaccine against Group A Streptococcus Palmieri, Elena Kis, Zoltán Ozanne, James Di Benedetto, Roberta Ricchetti, Beatrice Massai, Luisa Carducci, Martina Oldrini, Davide Gasperini, Gianmarco Aruta, Maria Grazia Rossi, Omar Kontoravdi, Cleo Shah, Nilay Mawas, Fatme Micoli, Francesca Vaccines (Basel) Article Group A Streptococcus (GAS) causes about 500,000 annual deaths globally, and no vaccines are currently available. The Group A Carbohydrate (GAC), conserved across all GAS serotypes, conjugated to an appropriate carrier protein, represents a promising vaccine candidate. Here, we explored the possibility to use Generalized Modules for Membrane Antigens (GMMA) as an alternative carrier system for GAC, exploiting their intrinsic adjuvant properties. Immunogenicity of GAC-GMMA conjugate was evaluated in different animal species in comparison to GAC-CRM(197); and the two conjugates were also compared from a techno-economic point of view. GMMA proved to be a good alternative carrier for GAC, resulting in a higher immune response compared to CRM(197) in different mice strains, as verified by ELISA and FACS analyses. Differently from CRM(197), GMMA induced significant levels of anti-GAC IgG titers in mice also in the absence of Alhydrogel. In rabbits, a difference in the immune response could not be appreciated; however, antibodies from GAC-GMMA-immunized animals showed higher affinity toward purified GAC antigen compared to those elicited by GAC-CRM(197). In addition, the GAC-GMMA production process proved to be more cost-effective, making this conjugate particularly attractive for low- and middle-income countries, where this pathogen has a huge burden. MDPI 2022-06-28 /pmc/articles/PMC9324507/ /pubmed/35891202 http://dx.doi.org/10.3390/vaccines10071034 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Palmieri, Elena Kis, Zoltán Ozanne, James Di Benedetto, Roberta Ricchetti, Beatrice Massai, Luisa Carducci, Martina Oldrini, Davide Gasperini, Gianmarco Aruta, Maria Grazia Rossi, Omar Kontoravdi, Cleo Shah, Nilay Mawas, Fatme Micoli, Francesca GMMA as an Alternative Carrier for a Glycoconjugate Vaccine against Group A Streptococcus |
title | GMMA as an Alternative Carrier for a Glycoconjugate Vaccine against Group A Streptococcus |
title_full | GMMA as an Alternative Carrier for a Glycoconjugate Vaccine against Group A Streptococcus |
title_fullStr | GMMA as an Alternative Carrier for a Glycoconjugate Vaccine against Group A Streptococcus |
title_full_unstemmed | GMMA as an Alternative Carrier for a Glycoconjugate Vaccine against Group A Streptococcus |
title_short | GMMA as an Alternative Carrier for a Glycoconjugate Vaccine against Group A Streptococcus |
title_sort | gmma as an alternative carrier for a glycoconjugate vaccine against group a streptococcus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9324507/ https://www.ncbi.nlm.nih.gov/pubmed/35891202 http://dx.doi.org/10.3390/vaccines10071034 |
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