The Immunogenicity of Capsid-Like Particle Vaccines in Combination with Different Adjuvants Using Different Routes of Administration

Capsid-like particle (CLP) displays can be used to enhance the immunogenicity of vaccine antigens, but a better understanding of how CLP vaccines are best formulated and delivered is needed. This study compared the humoral immune responses in mice elicited against two different vaccine antigens (a b...

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Main Authors: Christoph M. Janitzek, Philip H. R. Carlsen, Susan Thrane, Vijansh M. Khanna, Virginie Jakob, Christophe Barnier-Quer, Nicolas Collin, Thor G. Theander, Ali Salanti, Morten A. Nielsen, Adam F. Sander
Format: Article
Language:English
Published: MDPI AG 2021-02-01
Series:Vaccines
Subjects:
Online Access:https://www.mdpi.com/2076-393X/9/2/131
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spelling doaj-0008c113a9bf495698d73e1a4d92b23b2021-02-07T00:03:07ZengMDPI AGVaccines2076-393X2021-02-01913113110.3390/vaccines9020131The Immunogenicity of Capsid-Like Particle Vaccines in Combination with Different Adjuvants Using Different Routes of AdministrationChristoph M. Janitzek0Philip H. R. Carlsen1Susan Thrane2Vijansh M. Khanna3Virginie Jakob4Christophe Barnier-Quer5Nicolas Collin6Thor G. Theander7Ali Salanti8Morten A. Nielsen9Adam F. Sander10Centre for Medical Parasitology at the Department of Immunology and Microbiology, University of Copenhagen, 1165 København, DenmarkCentre for Medical Parasitology at the Department of Immunology and Microbiology, University of Copenhagen, 1165 København, DenmarkCentre for Medical Parasitology at the Department of Immunology and Microbiology, University of Copenhagen, 1165 København, DenmarkCentre for Medical Parasitology at the Department of Immunology and Microbiology, University of Copenhagen, 1165 København, DenmarkVaccine Formulation Institute, Plan-Les-Ouates, 1228 Geneva, SwitzerlandVaccine Formulation Laboratory, University of Lausanne, 1015 Lausanne, SwitzerlandVaccine Formulation Laboratory, University of Lausanne, 1015 Lausanne, SwitzerlandCentre for Medical Parasitology at the Department of Immunology and Microbiology, University of Copenhagen, 1165 København, DenmarkCentre for Medical Parasitology at the Department of Immunology and Microbiology, University of Copenhagen, 1165 København, DenmarkCentre for Medical Parasitology at the Department of Immunology and Microbiology, University of Copenhagen, 1165 København, DenmarkCentre for Medical Parasitology at the Department of Immunology and Microbiology, University of Copenhagen, 1165 København, DenmarkCapsid-like particle (CLP) displays can be used to enhance the immunogenicity of vaccine antigens, but a better understanding of how CLP vaccines are best formulated and delivered is needed. This study compared the humoral immune responses in mice elicited against two different vaccine antigens (a bacterial protein and a viral peptide) delivered on an AP205 CLP platform using six different adjuvant formulations. In comparison to antibody responses obtained after immunization with the unadjuvanted CLP vaccine, three of the adjuvant systems (neutral liposomes/monophosphoryl lipid A/quillaja saponaria 21, squalene-in-water emulsion, and monophosphoryl lipid A) caused significantly increased antibody levels, whereas formulation with the three other adjuvants (aluminum hydroxide, cationic liposomes, and cationic microparticles) resulted in similar or even decreased antibody responses. When delivering the soluble bacterial protein in a squalene-in-water emulsion, 4-log lower IgG levels were obtained compared to when the protein was delivered on CLPs without the adjuvant. The AP205 CLP platform promoted induction of both IgG1 and IgG2 subclasses, which could be skewed towards a higher production of IgG1 (aluminum hydroxide). Compared to other routes, intramuscular administration elicited the highest IgG levels. These results indicate that the effect of the external adjuvant does not always synergize with the adjuvant effect of the CLP display, which underscores the need for empirical testing of different extrinsic adjuvants.https://www.mdpi.com/2076-393X/9/2/131vaccinecapsid-like particlevirus-like particleadjuvantsAP205route of immunization
collection DOAJ
language English
format Article
sources DOAJ
author Christoph M. Janitzek
Philip H. R. Carlsen
Susan Thrane
Vijansh M. Khanna
Virginie Jakob
Christophe Barnier-Quer
Nicolas Collin
Thor G. Theander
Ali Salanti
Morten A. Nielsen
Adam F. Sander
spellingShingle Christoph M. Janitzek
Philip H. R. Carlsen
Susan Thrane
Vijansh M. Khanna
Virginie Jakob
Christophe Barnier-Quer
Nicolas Collin
Thor G. Theander
Ali Salanti
Morten A. Nielsen
Adam F. Sander
The Immunogenicity of Capsid-Like Particle Vaccines in Combination with Different Adjuvants Using Different Routes of Administration
Vaccines
vaccine
capsid-like particle
virus-like particle
adjuvants
AP205
route of immunization
author_facet Christoph M. Janitzek
Philip H. R. Carlsen
Susan Thrane
Vijansh M. Khanna
Virginie Jakob
Christophe Barnier-Quer
Nicolas Collin
Thor G. Theander
Ali Salanti
Morten A. Nielsen
Adam F. Sander
author_sort Christoph M. Janitzek
title The Immunogenicity of Capsid-Like Particle Vaccines in Combination with Different Adjuvants Using Different Routes of Administration
title_short The Immunogenicity of Capsid-Like Particle Vaccines in Combination with Different Adjuvants Using Different Routes of Administration
title_full The Immunogenicity of Capsid-Like Particle Vaccines in Combination with Different Adjuvants Using Different Routes of Administration
title_fullStr The Immunogenicity of Capsid-Like Particle Vaccines in Combination with Different Adjuvants Using Different Routes of Administration
title_full_unstemmed The Immunogenicity of Capsid-Like Particle Vaccines in Combination with Different Adjuvants Using Different Routes of Administration
title_sort immunogenicity of capsid-like particle vaccines in combination with different adjuvants using different routes of administration
publisher MDPI AG
series Vaccines
issn 2076-393X
publishDate 2021-02-01
description Capsid-like particle (CLP) displays can be used to enhance the immunogenicity of vaccine antigens, but a better understanding of how CLP vaccines are best formulated and delivered is needed. This study compared the humoral immune responses in mice elicited against two different vaccine antigens (a bacterial protein and a viral peptide) delivered on an AP205 CLP platform using six different adjuvant formulations. In comparison to antibody responses obtained after immunization with the unadjuvanted CLP vaccine, three of the adjuvant systems (neutral liposomes/monophosphoryl lipid A/quillaja saponaria 21, squalene-in-water emulsion, and monophosphoryl lipid A) caused significantly increased antibody levels, whereas formulation with the three other adjuvants (aluminum hydroxide, cationic liposomes, and cationic microparticles) resulted in similar or even decreased antibody responses. When delivering the soluble bacterial protein in a squalene-in-water emulsion, 4-log lower IgG levels were obtained compared to when the protein was delivered on CLPs without the adjuvant. The AP205 CLP platform promoted induction of both IgG1 and IgG2 subclasses, which could be skewed towards a higher production of IgG1 (aluminum hydroxide). Compared to other routes, intramuscular administration elicited the highest IgG levels. These results indicate that the effect of the external adjuvant does not always synergize with the adjuvant effect of the CLP display, which underscores the need for empirical testing of different extrinsic adjuvants.
topic vaccine
capsid-like particle
virus-like particle
adjuvants
AP205
route of immunization
url https://www.mdpi.com/2076-393X/9/2/131
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