Semisynthetic Pneumococcal Glycoconjugate ...
Type de document :
Article dans une revue scientifique: Article original
PMID :
Titre :
Semisynthetic Pneumococcal Glycoconjugate Nanovaccine
Auteur(s) :
Prasanna, Maruthi [Auteur]
Unité en Sciences Biologiques et Biotechnologies de Nantes [US2B]
Universidade de Santiago de Compostela [Spain] [USC ]
Varela Calvino, Rubén [Auteur]
Universidade de Santiago de Compostela [Spain] [USC ]
Lambert, Annie [Auteur]
Unité en Sciences Biologiques et Biotechnologies de Nantes [US2B]
Arista Romero, Maria [Auteur]
Institut de Química Avançada de Catalunya [CSIC] = Instituto de Química Avanzada de Cataluña [CSIC] = Institute of Advanced Chemistry of Catalonia [CSIC] [IQAC [CSIC]]
Pujals, Sylvia [Auteur]
Institut de Química Avançada de Catalunya [CSIC] = Instituto de Química Avanzada de Cataluña [CSIC] = Institute of Advanced Chemistry of Catalonia [CSIC] [IQAC [CSIC]]
Trottein, François [Auteur]
Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204 [CIIL]
Camberlein, Emilie [Auteur]
Unité en Sciences Biologiques et Biotechnologies de Nantes [US2B]
Grandjean, Cyrille [Auteur]
Unité en Sciences Biologiques et Biotechnologies de Nantes [US2B]
Csaba, Noemi [Auteur]
Universidade de Santiago de Compostela [Spain] [USC ]
Unité en Sciences Biologiques et Biotechnologies de Nantes [US2B]
Universidade de Santiago de Compostela [Spain] [USC ]
Varela Calvino, Rubén [Auteur]
Universidade de Santiago de Compostela [Spain] [USC ]
Lambert, Annie [Auteur]
Unité en Sciences Biologiques et Biotechnologies de Nantes [US2B]
Arista Romero, Maria [Auteur]
Institut de Química Avançada de Catalunya [CSIC] = Instituto de Química Avanzada de Cataluña [CSIC] = Institute of Advanced Chemistry of Catalonia [CSIC] [IQAC [CSIC]]
Pujals, Sylvia [Auteur]
Institut de Química Avançada de Catalunya [CSIC] = Instituto de Química Avanzada de Cataluña [CSIC] = Institute of Advanced Chemistry of Catalonia [CSIC] [IQAC [CSIC]]
Trottein, François [Auteur]
Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204 [CIIL]
Camberlein, Emilie [Auteur]
Unité en Sciences Biologiques et Biotechnologies de Nantes [US2B]
Grandjean, Cyrille [Auteur]
Unité en Sciences Biologiques et Biotechnologies de Nantes [US2B]
Csaba, Noemi [Auteur]
Universidade de Santiago de Compostela [Spain] [USC ]
Titre de la revue :
Bioconjugate Chemistry
Pagination :
1563-1575
Éditeur :
American Chemical Society
Date de publication :
2023-09-11
ISSN :
1043-1802
Mot(s)-clé(s) en anglais :
Biopolymers
Glycoconjugate vaccine
Immunology
Rodent models
Vaccination
Pneumococcus
Glycoconjugate vaccine
Immunology
Rodent models
Vaccination
Pneumococcus
Discipline(s) HAL :
Sciences du Vivant [q-bio]
Chimie
Chimie
Résumé en anglais : [en]
Pneumococcal conjugate vaccines offer an excellent safety profile and high protection against the serotypes comprised in the vaccine. However, inclusion of protein antigens from Streptococcus pneumoniaecombined with potent ...
Lire la suite >Pneumococcal conjugate vaccines offer an excellent safety profile and high protection against the serotypes comprised in the vaccine. However, inclusion of protein antigens from Streptococcus pneumoniaecombined with potent adjuvants and a suitable delivery system are expected to both extend protection to serotype strains not represented in the formulation and stimulate a broader immune response, thus more effective in young children, elderly, and immunocompromised populations. Along this line, nanoparticle (NP) delivery systems can enhance the immunogenicity of antigens by protecting them from degradation and increasing their uptake by antigen-presenting cells, as well as offering co-delivery with adjuvants. We report herein the encapsulation of a semisynthetic glycoconjugate (GC) composed of a synthetic tetrasaccharide mimicking theS. pneumoniae serotype 14 capsular polysaccharide (CP14) linked to the Pneumococcal surface protein A (PsaA) using chitosan NPs (CNPs). These GC-loaded chitosan nanoparticles (GC-CNPs) were not toxic to human monocyte-derived dendritic cells (MoDCs), showed enhanced uptake, and displayed better immunostimulatory properties in comparison to the naked GC. A comparative study was carried out in mice to evaluate the immune response elicited by the glycoconjugate-administered subcutaneously (SC), where the GC-CNPs displayed 100-fold higher IgG response as compared with the group treated with nonencapsulated GC. Overall, the study demonstrates the potential of this chitosan-based nanovaccine for efficient delivery of glycoconjugate antigens.Lire moins >
Lire la suite >Pneumococcal conjugate vaccines offer an excellent safety profile and high protection against the serotypes comprised in the vaccine. However, inclusion of protein antigens from Streptococcus pneumoniaecombined with potent adjuvants and a suitable delivery system are expected to both extend protection to serotype strains not represented in the formulation and stimulate a broader immune response, thus more effective in young children, elderly, and immunocompromised populations. Along this line, nanoparticle (NP) delivery systems can enhance the immunogenicity of antigens by protecting them from degradation and increasing their uptake by antigen-presenting cells, as well as offering co-delivery with adjuvants. We report herein the encapsulation of a semisynthetic glycoconjugate (GC) composed of a synthetic tetrasaccharide mimicking theS. pneumoniae serotype 14 capsular polysaccharide (CP14) linked to the Pneumococcal surface protein A (PsaA) using chitosan NPs (CNPs). These GC-loaded chitosan nanoparticles (GC-CNPs) were not toxic to human monocyte-derived dendritic cells (MoDCs), showed enhanced uptake, and displayed better immunostimulatory properties in comparison to the naked GC. A comparative study was carried out in mice to evaluate the immune response elicited by the glycoconjugate-administered subcutaneously (SC), where the GC-CNPs displayed 100-fold higher IgG response as compared with the group treated with nonencapsulated GC. Overall, the study demonstrates the potential of this chitosan-based nanovaccine for efficient delivery of glycoconjugate antigens.Lire moins >
Langue :
Anglais
Comité de lecture :
Oui
Audience :
Internationale
Vulgarisation :
Non
Projet Européen :
Source :
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