Key result
Monoclonal antibodies BD70-4003 and BD70-4017 provide 100% protection against SFTSV in a lethal mouse model.
Why the study?
Severe fever with thrombocytopenia syndrome virus (SFTSV) is a lethal bunyavirus lacking approved countermeasures.
Identification of potent human monoclonal antibodies against SFTSV Gn head that provide 100% protection in a lethal mouse model, offering potential therapeutic candidates.
Should not yet change SFTSV clinical practice; supports Gn head mAbs as therapeutic candidates for further development.
Severe fever with thrombocytopenia syndrome virus (SFTSV) is a lethal bunyavirus lacking approved countermeasures. From SFTS survivors, we isolate 84 human monoclonal antibodies (mAbs) against the viral glycoproteins Gn and Gc. Gn-specific mAbs demonstrate superior neutralization breadth and potency compared to the restricted neutralizing activity observed with Gc. Using a high-throughput yeast display deep mutational scanning (DMS) platform, we classify Gn-head mAbs into eight epitope groups, among which four groups (IA, ID, IIIA, and IIIB) confer neutralization. Notably, mAbs BD70-4003 (group IA) and BD70-4017 (group IIIA) exhibit broad neutralization and provide 100% protection in a lethal mouse model. Cryo-electron microscopy (cryo-EM) structural analysis of these mAbs in complex with the Gn head reveals their binding interfaces, directly validating the epitope residues identified by DMS. Our study delineates the antigenic landscape of SFTSV Gn, identifies potent therapeutic candidates, and establishes DMS coupled with structural validation as a powerful framework for antibody discovery against bunyaviruses.
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Wang et al. (2026) studied this question. Monoclonal antibodies BD70-4003 and BD70-4017 targeting the SFTSV Gn head exhibited broad neutralization and provided 100% protection against the virus in a lethal mouse model.
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