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Efficacy of Multivalent Dengue Vaccine Candidates Predicted In Silico
Seokhwan Hyeon1, Kwangwook Kim1, Yoo Jin Na1
1Division of Vaccine Development, Center for Vaccine Research National Institute of Infectious Diseases, Korea National Institute of Health, Korea Disease Control and Prevention Agency, Cheongju 28159, Republic of Korea.
Vaccines
|February 26, 2026
Summary
This study identifies immunogenic peptides from the Dengue virus (DENV) envelope protein. These peptides stimulate cellular immunity and cytokine production, offering potential for new DENV vaccines.
Area of Science:
- Virology
- Immunology
- Vaccine Development
Background:
- Dengue virus (DENV) poses a growing global health threat.
- The immunogenicity of DENV structural proteins remains incompletely understood, hindering vaccine design.
Purpose of the Study:
- To predict and evaluate the immunogenicity of DENV structural proteins, particularly the envelope protein.
- To identify potential vaccine candidates by assessing T-cell mediated immune responses.
Main Methods:
- In silico prediction of B-cell and T-cell epitopes using BepiPred-2.0 and IEDB.
- In vitro validation through T-cell proliferation assays.
- In vivo assessment in mice using ELISpot, qRT-PCR, and plaque reduction neutralization tests.
Main Results:
- Identified nine-amino-acid peptide candidates with high immunogenicity scores.
- Confirmed T-cell stimulation and significant cytokine regulation (IFN-γ, TNF-α, IL-4) in vaccinated mice.
- Demonstrated induction of cellular immunity via plaque reduction neutralization tests.
Conclusions:
- Selected DENV envelope protein peptides elicit robust cellular immune responses.
- These findings support the development of epitope-based vaccines against Dengue virus.
Keywords:
antigen presentationcellular immunitycytokinesdengue vaccinesepitopeshumoral immunityimmunizationneutralizing antibodiesprotein subunit vaccinesviral structural proteins
