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  3. Targeted Lymph Node Immunization with Serotype-Specific Dengue VLP Vaccines Enhances Antibody Avidity and Specificity.
 

Targeted Lymph Node Immunization with Serotype-Specific Dengue VLP Vaccines Enhances Antibody Avidity and Specificity.

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Description
Dominik A. Rothen and Alessandro Pardini contributed equally to this work.
BORIS DOI
10.48620/91550
Publisher DOI
10.3390/vaccines13090941
PubMed ID
41012144
Description
Introduction
Dengue virus (DENV) remains a global health threat, with four distinct serotypes (DENV1-4) that complicate vaccine development due to low-affinity, cross-reactive antibodies that increase the risk of antibody-dependent enhancement (ADE).
Objective
To address the challenge of inducing strictly serotype-specific immune responses, this study explored the use of targeting individual lymph nodes (LNs) for the creation of simultaneous but independent immune responses as a targeted approach to reduce cross-reactivity and improve vaccine specificity.
Methods
In the initial experiments, targeting individual LN successfully induced specific germinal centers (GCs) for different antigens in distinct LNs, highlighting its potential to enhance immune specificity. This approach was further tested using two virus-like particle (VLP)-based vaccines based on AP205 for DENV1 and DENV4, selected due to their genetic divergence and to probe the potential to minimize cross-reactive immune responses. In this setup, AP205-DV1 and AP205-DV4 were administered in targeted separate LNs, and the specificity of the immune response was compared to subcutaneous administration of a mixture of both vaccines.
Results
Our data show that targeting distinct LNs elicited antibodies with significantly higher avidity, which is a critical factor in determining the neutralizing capacity of the immune response. Avidity measurements confirmed that this segregation approach results in a more refined selection of high-affinity B cells. Neutralization experiments demonstrated that targeting distinct LNs with individual vaccines induced a more potent and serotype-specific neutralizing response, compared to the injection of a vaccine mixture.
Conclusions
These findings suggest that targeting individual LNs could be a promising method for enhancing both the specificity and potency of immune responses, particularly for flaviviruses. Targeting distinct LNs by direct administration of individual vaccines into distinct watersheds rather than individual lymph nodes will offer the opportunity to facilitate the approach in humans.
Date of Publication
2025-09-03
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
Keyword(s)
AP205
•
VLP
•
dengue
•
flaviviruses
•
lymph node
•
vaccine
•
virus
•
virus-like particle
Language(s)
en
Contributor(s)
Rothen, Dominik A.
Universitätsklinik für Rheumatologie und Immunologie - Gruppe Bachmann Anna-Seiler-Haus
Department for BioMedical Research, Forschungsgruppe Rheumatologie
Pardini, Alessandroorcid-logo
Universitätsklinik für Rheumatologie und Immunologie - Gruppe Bachmann Anna-Seiler-Haus
Department for BioMedical Research, Forschungsgruppe Rheumatologie
Dutta, Sudip Kumar
Krenger, Pascal S.
Universitätsklinik für Rheumatologie und Immunologie - Gruppe Bachmann
Department for BioMedical Research, Forschungsgruppe Rheumatologie
Vogt, Anne-Cathrine
Universitätsklinik für Rheumatologie und Immunologie - Fachbereich Immunologie Anna-Seiler-Haus
Clinic of Rheumatology and Immunology
Josi, Romano
Universitätsklinik für Rheumatologie und Immunologie - Gruppe Bachmann Anna-Seiler-Haus
Department for BioMedical Research, Forschungsgruppe Rheumatologie
Vogel, Monique
Department for BioMedical Research (DBMR)
Clinic of Rheumatology and Immunology
Department for BioMedical Research, Forschungsgruppe Rheumatologie
Engeroff, Paulorcid-logo
Department for BioMedical Research, Forschungsgruppe Rheumatologie
Universitätsklinik für Rheumatologie und Immunologie - Fachbereich Immunologie
Mohsen, Mona O.
Universitätsklinik für Rheumatologie und Immunologie - Gruppe Bachmann Anna-Seiler-Haus
Department for BioMedical Research, Forschungsgruppe Rheumatologie
Tars, Kaspars
Martina, Byron
Bachmann, Martin F.
Clinic of Rheumatology and Immunology
Department for BioMedical Research, Forschungsgruppe Rheumatologie
Additional Credits
Universitätsklinik für Rheumatologie und Immunologie - Gruppe Bachmann Anna-Seiler-Haus
Universitätsklinik für Rheumatologie und Immunologie - Fachbereich Immunologie Anna-Seiler-Haus
Department for BioMedical Research, Forschungsgruppe Rheumatologie
Clinic of Rheumatology and Immunology
Graduate School for Cellular and Biomedical Sciences (GCB)
Department for BioMedical Research (DBMR)
Universitätsklinik für Rheumatologie und Immunologie - Fachbereich Rheumatologie
Series
Vaccines
Publisher
MDPI
ISSN
2076-393X
Access(Rights)
open.access
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