Polyacrylate–Peptide Antigen Conjugate as a Single-Dose Oral Vaccine against Group A <i>Streptococcus</i>

Group A <i>Streptococcus</i> (GAS)-associated rheumatic heart disease is a leading cause of death caused by GAS infection. While antibiotics can treat the infection in most cases, growing antibiotic resistance, late medical intervention, and recurrent infection are major obstacles to the...

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Main Authors: Mohammad Omer Faruck, Lili Zhao, Waleed M. Hussein, Zeinab G. Khalil, Robert J. Capon, Mariusz Skwarczynski, Istvan Toth
Format: Article
Language:English
Published: MDPI AG 2020-01-01
Series:Vaccines
Subjects:
Online Access:https://www.mdpi.com/2076-393X/8/1/23
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author Mohammad Omer Faruck
Lili Zhao
Waleed M. Hussein
Zeinab G. Khalil
Robert J. Capon
Mariusz Skwarczynski
Istvan Toth
author_facet Mohammad Omer Faruck
Lili Zhao
Waleed M. Hussein
Zeinab G. Khalil
Robert J. Capon
Mariusz Skwarczynski
Istvan Toth
author_sort Mohammad Omer Faruck
collection DOAJ
description Group A <i>Streptococcus</i> (GAS)-associated rheumatic heart disease is a leading cause of death caused by GAS infection. While antibiotics can treat the infection in most cases, growing antibiotic resistance, late medical intervention, and recurrent infection are major obstacles to the effective treatment of GAS-associated diseases. As GAS infection typically originates from the bacterial colonization of mucosal tissue in the throat, an oral vaccine that can generate both systemic and mucosal immune responses would solve problems associated with traditional medical interventions. Moreover, orally delivered vaccines are more easily administered and less expensive for mass immunization. In this study, the B-cell epitope J8, derived from GAS M protein, and universal T-helper Pan HLA-DR-binding epitope peptide (PADRE), were conjugated to poly (methyl acrylate) (PMA) to form a self-assembled nanoparticle vaccine candidate (PMA-P-J8). Strong systemic and mucosal immune responses were induced upon single oral immunization of mice with the conjugate. The antibodies generated were opsonic against GAS clinical isolates as measured after boost immunization. Thus, we developed a simple conjugate as an effective, adjuvant-free oral peptide-based vaccine.
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spelling doaj.art-f1b76c83d3d540dfb4de265e12d40fb92022-12-22T03:19:23ZengMDPI AGVaccines2076-393X2020-01-01812310.3390/vaccines8010023vaccines8010023Polyacrylate–Peptide Antigen Conjugate as a Single-Dose Oral Vaccine against Group A <i>Streptococcus</i>Mohammad Omer Faruck0Lili Zhao1Waleed M. Hussein2Zeinab G. Khalil3Robert J. Capon4Mariusz Skwarczynski5Istvan Toth6School of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, Brisbane, QLD 4072, AustraliaSchool of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, Brisbane, QLD 4072, AustraliaSchool of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, Brisbane, QLD 4072, AustraliaInstitute for Molecular Bioscience, The University of Queensland, St. Lucia, QLD 4072, AustraliaInstitute for Molecular Bioscience, The University of Queensland, St. Lucia, QLD 4072, AustraliaSchool of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, Brisbane, QLD 4072, AustraliaSchool of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, Brisbane, QLD 4072, AustraliaGroup A <i>Streptococcus</i> (GAS)-associated rheumatic heart disease is a leading cause of death caused by GAS infection. While antibiotics can treat the infection in most cases, growing antibiotic resistance, late medical intervention, and recurrent infection are major obstacles to the effective treatment of GAS-associated diseases. As GAS infection typically originates from the bacterial colonization of mucosal tissue in the throat, an oral vaccine that can generate both systemic and mucosal immune responses would solve problems associated with traditional medical interventions. Moreover, orally delivered vaccines are more easily administered and less expensive for mass immunization. In this study, the B-cell epitope J8, derived from GAS M protein, and universal T-helper Pan HLA-DR-binding epitope peptide (PADRE), were conjugated to poly (methyl acrylate) (PMA) to form a self-assembled nanoparticle vaccine candidate (PMA-P-J8). Strong systemic and mucosal immune responses were induced upon single oral immunization of mice with the conjugate. The antibodies generated were opsonic against GAS clinical isolates as measured after boost immunization. Thus, we developed a simple conjugate as an effective, adjuvant-free oral peptide-based vaccine.https://www.mdpi.com/2076-393X/8/1/23peptide vaccinepoly (methyl acrylate)oral deliverynanoparticlespolymer–peptide conjugategroup a <i>streptococcus</i>
spellingShingle Mohammad Omer Faruck
Lili Zhao
Waleed M. Hussein
Zeinab G. Khalil
Robert J. Capon
Mariusz Skwarczynski
Istvan Toth
Polyacrylate–Peptide Antigen Conjugate as a Single-Dose Oral Vaccine against Group A <i>Streptococcus</i>
Vaccines
peptide vaccine
poly (methyl acrylate)
oral delivery
nanoparticles
polymer–peptide conjugate
group a <i>streptococcus</i>
title Polyacrylate–Peptide Antigen Conjugate as a Single-Dose Oral Vaccine against Group A <i>Streptococcus</i>
title_full Polyacrylate–Peptide Antigen Conjugate as a Single-Dose Oral Vaccine against Group A <i>Streptococcus</i>
title_fullStr Polyacrylate–Peptide Antigen Conjugate as a Single-Dose Oral Vaccine against Group A <i>Streptococcus</i>
title_full_unstemmed Polyacrylate–Peptide Antigen Conjugate as a Single-Dose Oral Vaccine against Group A <i>Streptococcus</i>
title_short Polyacrylate–Peptide Antigen Conjugate as a Single-Dose Oral Vaccine against Group A <i>Streptococcus</i>
title_sort polyacrylate peptide antigen conjugate as a single dose oral vaccine against group a i streptococcus i
topic peptide vaccine
poly (methyl acrylate)
oral delivery
nanoparticles
polymer–peptide conjugate
group a <i>streptococcus</i>
url https://www.mdpi.com/2076-393X/8/1/23
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