Target intelligence / Profile preview

Dabie bandavirus antigen (DBV antigen (or SFTSV antigen, as SFTSV is widely used synonymously for this virus))

Target
DBV antigen (or SFTSV antigen, as SFTSV is widely used synonymously for this virus)
Molecular classification
Viral antigen, Structural protein (includes Gn, Gc, NP), Non-structural protein (NSs), Membrane protein (Gn, Gc)
01

Overview

Dabie bandavirus antigens are proteins expressed by Dabie bandavirus (SFTSV), a tick-borne member of the Phenuiviridae family and genus Bandavirus, and primary causative agent of severe fever with thrombocytopenia syndrome (SFTS). The viral genome is segmented and encodes several immunogenic proteins including: Gn and Gc glycoproteins (M segment): major structural and surface antigens, critical for viral attachment and membrane fusion. These are targets for host neutralizing antibodies and are of key interest for vaccine development. Host cell entry occurs via interaction with surface receptors such as DC-SIGN. Nucleocapsid protein (NP, S segment): encapsidates viral RNA, has high immunogenicity, and is the main target for diagnostic antibodies, but antibodies against NP are generally non-neutralizing. Nonstructural protein (NSs, S segment): plays a role in immune evasion by inhibiting interferon signaling, and can manipulate host cell machinery to benefit the virus. Serological assays for DBV antigens are core to current lab diagnosis of SFTS. Vaccine research efforts are ongoing, primarily targeting the Gn and Gc proteins for their role in virus neutralization. DBV antigenic variation requires careful vaccine and diagnostic design to ensure broad efficacy across genotypes.

Other names
Severe fever with thrombocytopenia syndrome virus antigenSFTSV antigenSevere fever with thrombocytopenia syndrome virus (SFTSV)Bandavirus dabieense antigenSFTS virus antigen
02

Mechanism of action

Neutralizing antibodies bind to Gn and Gc, blocking viral entry and fusion. Non-neutralizing antibodies bind to NP, useful for diagnosis, but do not block viral infection. Vaccine-induced immune responses target surface antigens (Gn/Gc) to promote immunity.

03

Biological functions

Virus entry and membrane fusion (Gn and Gc)Recognition by host immune system, target for neutralizing antibodies (Gn, Gc, NP)Inhibition of host innate immune response (NSs suppresses interferon signaling)Genome protection and replication (NP)
04

Disease associations

Infection (severe fever with thrombocytopenia syndrome)Potential for multiorgan failure, hemorrhagic fever
05

Safety considerations

Antigenic variation/genetic diversity among DBV strains complicates diagnostic and vaccine coverageNo licensed vaccine; current exposure risk from tick bite, and human-to-human transmission is possible in certain settings
06

Interacting drugs

Monoclonal antibodies (under development for diagnostics and experimental therapeutics)

1 more in the full profile.

07

Biomarkers

Gn, Gc, and NP antigens (used in serological diagnosis)Antibody titers to DBV antigens used for monitoring infection and vaccine efficacy

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