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Dengue virus peptide epitopes are specific amino acid sequences within the Dengue virus (DENV) polyprotein that are recognized by the host's immune system, specifically B-cells and T-cells (Immune Epitope Database, 2024). These epitopes are derived from both structural proteins (Envelope, Membrane, and Capsid) and non-structural proteins (NS1, NS2A, NS2B, NS3, NS4A, NS4B, and NS5) (WHO, 2023). The Envelope (E) protein contains critical B-cell epitopes that are the primary targets for neutralizing antibodies, while non-structural proteins like NS3 and NS5 are rich in T-cell epitopes essential for cellular immunity (PubMed, PMID: 24103314). In the context of vaccine development, these epitopes are the functional targets used to elicit a protective immune response against all four DENV serotypes (Nature Reviews Drug Discovery, 2020). However, the presence of certain epitopes can also lead to antibody-dependent enhancement (ADE), where sub-neutralizing antibodies facilitate viral entry into Fc-receptor-bearing cells, complicating therapeutic strategies (Science, 2016). Understanding the landscape of these epitopes is vital for designing next-generation vaccines and monoclonal antibody therapies that provide broad protection without increasing the risk of severe disease (Cell, 2015).
Induction of neutralizing antibodies and cellular immune responses to prevent viral entry and clear infected cells.
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