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Development of Multilayer Nanoparticles for the Delivery of Peptide-Based Subunit Vaccine against Group A Streptococcus
Peptide-based subunit vaccines include only minimal antigenic determinants, and, therefore, are less likely to induce allergic immune responses and adverse effects compared to traditional vaccines. However, peptides are weakly immunogenic and susceptible to enzymatic degradation when administered on...
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/PMC9610843/ https://www.ncbi.nlm.nih.gov/pubmed/36297584 http://dx.doi.org/10.3390/pharmaceutics14102151 |
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author | Kiong, Jolynn Nahar, Ummey Jannatun Jin, Shengbin Shalash, Ahmed O. Zhang, Jiahui Koirala, Prashamsa Khalil, Zeinab G. Capon, Robert J. Skwarczynski, Mariusz Toth, Istvan Hussein, Waleed M. |
author_facet | Kiong, Jolynn Nahar, Ummey Jannatun Jin, Shengbin Shalash, Ahmed O. Zhang, Jiahui Koirala, Prashamsa Khalil, Zeinab G. Capon, Robert J. Skwarczynski, Mariusz Toth, Istvan Hussein, Waleed M. |
author_sort | Kiong, Jolynn |
collection | PubMed |
description | Peptide-based subunit vaccines include only minimal antigenic determinants, and, therefore, are less likely to induce allergic immune responses and adverse effects compared to traditional vaccines. However, peptides are weakly immunogenic and susceptible to enzymatic degradation when administered on their own. Hence, we designed polyelectrolyte complex (PEC)-based delivery systems to protect peptide antigens from degradation and improve immunogenicity. Lipopeptide (LCP-1) bearing J8 B-cell epitope derived from Group A Streptococcus (GAS) M-protein was selected as the model peptide antigen. In the pilot study, LCP-1 incorporated in alginate/cross-linked polyarginine-J8-based PEC induced high J8-specific IgG antibody titres. The PEC system was then further modified to improve its immune stimulating capability. Of the formulations tested, PEC-4, bearing LCP-1, alginate and cross-linked polylysine, induced the highest antibody titres in BALB/c mice following subcutaneous immunisation. The antibodies produced were more opsonic than those induced by mice immunised with other PECs, and as opsonic as those induced by antigen adjuvanted with powerful complete Freund’s adjuvant. |
format | Online Article Text |
id | pubmed-9610843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96108432022-10-28 Development of Multilayer Nanoparticles for the Delivery of Peptide-Based Subunit Vaccine against Group A Streptococcus Kiong, Jolynn Nahar, Ummey Jannatun Jin, Shengbin Shalash, Ahmed O. Zhang, Jiahui Koirala, Prashamsa Khalil, Zeinab G. Capon, Robert J. Skwarczynski, Mariusz Toth, Istvan Hussein, Waleed M. Pharmaceutics Article Peptide-based subunit vaccines include only minimal antigenic determinants, and, therefore, are less likely to induce allergic immune responses and adverse effects compared to traditional vaccines. However, peptides are weakly immunogenic and susceptible to enzymatic degradation when administered on their own. Hence, we designed polyelectrolyte complex (PEC)-based delivery systems to protect peptide antigens from degradation and improve immunogenicity. Lipopeptide (LCP-1) bearing J8 B-cell epitope derived from Group A Streptococcus (GAS) M-protein was selected as the model peptide antigen. In the pilot study, LCP-1 incorporated in alginate/cross-linked polyarginine-J8-based PEC induced high J8-specific IgG antibody titres. The PEC system was then further modified to improve its immune stimulating capability. Of the formulations tested, PEC-4, bearing LCP-1, alginate and cross-linked polylysine, induced the highest antibody titres in BALB/c mice following subcutaneous immunisation. The antibodies produced were more opsonic than those induced by mice immunised with other PECs, and as opsonic as those induced by antigen adjuvanted with powerful complete Freund’s adjuvant. MDPI 2022-10-10 /pmc/articles/PMC9610843/ /pubmed/36297584 http://dx.doi.org/10.3390/pharmaceutics14102151 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 Kiong, Jolynn Nahar, Ummey Jannatun Jin, Shengbin Shalash, Ahmed O. Zhang, Jiahui Koirala, Prashamsa Khalil, Zeinab G. Capon, Robert J. Skwarczynski, Mariusz Toth, Istvan Hussein, Waleed M. Development of Multilayer Nanoparticles for the Delivery of Peptide-Based Subunit Vaccine against Group A Streptococcus |
title | Development of Multilayer Nanoparticles for the Delivery of Peptide-Based Subunit Vaccine against Group A Streptococcus |
title_full | Development of Multilayer Nanoparticles for the Delivery of Peptide-Based Subunit Vaccine against Group A Streptococcus |
title_fullStr | Development of Multilayer Nanoparticles for the Delivery of Peptide-Based Subunit Vaccine against Group A Streptococcus |
title_full_unstemmed | Development of Multilayer Nanoparticles for the Delivery of Peptide-Based Subunit Vaccine against Group A Streptococcus |
title_short | Development of Multilayer Nanoparticles for the Delivery of Peptide-Based Subunit Vaccine against Group A Streptococcus |
title_sort | development of multilayer nanoparticles for the delivery of peptide-based subunit vaccine against group a streptococcus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9610843/ https://www.ncbi.nlm.nih.gov/pubmed/36297584 http://dx.doi.org/10.3390/pharmaceutics14102151 |
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