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Updated: May 8, 2026

A Murine Model of Dengue Virus-induced Acute Viral Encephalitis-like Disease
Published on: April 28, 2019
Nanobody conjugated with dendrimer nanoparticles effectively neutralizes tick-borne encephalitis virus
Jana Jozefiaková1, Amod Kulkarni1,2, Dinesh Dhumal3
1Laboratory of Biomedical Microbiology and Immunology, University of Veterinary Medicine and Pharmacy in Košice, Komenského 73, Košice, 04181, Slovakia.
None:
Tick-borne encephalitis virus (TBEV) is a neurotropic flavivirus causing severe meningitis, encephalitis, or meningoencephalitis. The blood-brain barrier (BBB) prevents therapeutic agents from reaching the brain; therefore, specific antiviral therapy that can cross the BBB and treat TBEV-induced infection is urgently needed. In this study, nanobodies (NBs) targeting domain III (DIII) of the envelope (E) glycoprotein of TBEV were developed and conjugated to drug delivery nanosystems based on self-assembling dendrimer nanomicelles (DNs) and gold nanoparticles (AuNs) to facilitate BBB passage and viral neutralization. NBs were derived from the variable region of heavy chain-only llama antibodies and panned against DIII using phage display. The most active NBs were conjugated with DNs and AuNs. Remarkably, the dendrimer nanosystem decorated with the nanobody clone TA3 (TA3-DNs) and the peptide Angiopep-2 effectively crossed the BBB model and neutralized TBEV. Therefore, TA3-DNs constitute a promising candidate for treating TBEV, and merit further validation in animal models for future translational studies.
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