Frontiers in Cellular and Infection Microbiology· 2026Q1· Review
Preclinical models of Bandavirus dabieense infection: insights into pathogenesis, host responses, and translational applications
- 0citations
- Q1SCImago
- 2026year
Short summary
This review critically evaluates current cellular and animal models for Bandavirus dabieense (DBV), the pathogen causing SFTS, highlighting their strengths and limitations in recapitulating human disease features for research into viral replication, host responses, and antiviral efficacy.
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Key points
- Bandavirus dabieense (DBV) causes SFTS, a significant emerging tick-borne illness with no approved antiviral therapies.
- A range of preclinical models, from cell lines to non-human primates, are available for DBV research.
- Each model system has distinct strengths and limitations in recapitulating key aspects of human DBV infection.
- Current models are crucial for investigating viral pathogenesis, host immune responses, and evaluating antiviral efficacy.
- There are significant gaps in the current model landscape, necessitating improvements for greater translational value.
AI-generated from the title and abstract; the full text is not read.
Abstract
Bandavirus dabieense (DBV), the causative agent of severe fever with thrombocytopenia syndrome (SFTS), is an emerging tick-borne pathogen associated with substantial morbidity and mortality. Despite increasing incidence across East and Southeast Asia, the pathogenic mechanisms of DBV infection remain incompletely understood, and no specific antiviral therapies have been approved. Robust preclinical models are therefore essential for elucidating viral pathogenesis and accelerating therapeutic and vaccine development. In this Review, we summarize recent advances in cellular and animal models of DBV infection, including established cell lines, primary cells, interferon-deficient rodents, hamsters, ferrets, companion animals, and non-human primates. We critically evaluate the strengths and limitations of these systems in recapitulating key features of human disease and discuss their utility for investigating viral replication, host responses, inflammatory injury, and antiviral efficacy. We further highlight major gaps in the current model landscape and propose priorities for improving the physiological relevance and translational value of DBV experimental systems.
The authors' abstract, as published at the source. Frontiers in Cellular and Infection Microbiology, 2026 · DOI ↗
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Field: Infectious Diseases
Infectious DiseasesMedicine