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DOI 10.1016/j.ijid.2026.108771

Медицинская библиотека · International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2026

Dengue antibody dynamics resolved at epitope level using a dengue 1 human infection model.

Bouckaert Johanna, Waickman Adam T, Thomas Stephen J, Ariën Kevin K, Lagatie Ole

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Аннотация

OBJECTIVES

To characterize longitudinal antibody responses at the epitope level following primary dengue virus serotype 1 (DENV1) infection in a controlled human infection model, and to identify antigenic regions that could guide the development of improved dengue serodiagnostics.

METHODS

In this study, we leveraged samples from a dengue human infection model, in which nine flavivirus-naïve individuals were experimentally infected with the under-attenuated DENV1 strain 45AZ5. IgM and IgG reactivity to 7888 overlapping 15-mer peptides spanning the dengue, Zika, yellow fever, and chikungunya virus proteomes was evaluated using peptide microarrays. Top candidates were validated using multiplex peptide immunoassays.

RESULTS

Primary DENV1 infection elicited responses primarily targeting the DENV proteome, including antigenic regions in both structural and non-structural proteins. Several known and novel antigenic regions showed elevated reactivity upon primary infection, notably the highly reactive NS1 wing domain epitope with distinct IgM and IgG profiles in early and late convalescent phases.

CONCLUSIONS

These findings provide detailed insight into humoral responses following primary DENV1 infection and highlight specific linear B cell epitopes and antigenic regions that could inform the development of improved diagnostic tests based on defined linear B cell epitopes.

Для цитирования: Bouckaert Johanna, Waickman Adam T, Thomas Stephen J, Ariën Kevin K, Lagatie Ole. Dengue antibody dynamics resolved at epitope level using a dengue 1 human infection model.. International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases. 2026. DOI: 10.1016/j.ijid.2026.108771.

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