Target intelligence / Profile preview

Influenza B virus hemagglutinin (HA) (Victoria lineage) (HA)

Target
HA
Molecular classification
Receptor, Other
01

Overview

Influenza B virus hemagglutinin (HA) is a primary surface glycoprotein essential for the viral infection cycle, specifically within the Victoria lineage (often designated as Lineage 2). HA functions as a homotrimeric class I fusion protein that mediates both host cell attachment and membrane fusion (UniProt P03460). The protein's head domain binds to sialic acid receptors on the respiratory epithelium, while the stem domain undergoes a dramatic conformational change at low pH to facilitate viral entry (PubMed 25733861). As the dominant antigen on the viral surface, HA is the primary target for neutralizing antibodies induced by seasonal quadrivalent influenza vaccines (CDC, 2023). Therapeutic efforts targeting this molecule include the development of broadly neutralizing monoclonal antibodies, such as CR9114, which bind to the conserved stem region to prevent fusion across multiple influenza lineages (Science, 2012). Additionally, small-molecule inhibitors like Umifenovir target the HA-mediated fusion process to inhibit viral replication (PubMed 30812941). The continuous evolution of HA through antigenic drift remains a significant challenge, necessitating ongoing surveillance and periodic vaccine strain updates to maintain clinical efficacy.

Other names
Influenza B hemagglutinin – B lineage 2B/Victoria/2/87-like hemagglutininLineage II hemagglutininVictoria lineage HAHemagglutinin
02

Mechanism of action

Inhibition of viral attachment and membrane fusion

03

Biological functions

Immune responseOther
04

Disease associations

Infection
05

Safety considerations

Antigenic driftEgg-adaptive mutationsLineage mismatch in vaccines
06

Interacting drugs

Umifenovir

3 more in the full profile.

07

Biomarkers

Hemagglutination inhibition (HAI) titerMicroneutralization (MN) titerHA-specific IgG levels

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