Antibodies against influenza viruses primarily target hemagglutinin (HA) or neuraminidase (NA) surface proteins. These antibodies are categorized by their binding regions and functional mechanisms:
6F12 Antibody: Neutralizes H1 viruses spanning 79 years of antigenic drift. Prevents weight loss in mice at low doses (0.3–0.9 mg/kg) and binds the HA stalk via a conformational epitope .
CR6261: Targets group 1 HAs (H1, H5) and protects against lethal H1N1 challenge in mice .
KPF1: Binds a conserved epitope on the H1 HA globular head, neutralizing 83% of tested H1 isolates (including 1918 H1N1). In vivo efficacy includes 100% survival in prophylactic mouse models .
FNI9: Inhibits NA activity across all group 1 and 2 IAVs. Prophylactic administration (0.3 mg/kg) fully protects mice from H1N1 challenge without requiring Fc-mediated effector functions .
HA Stalk Antibodies: Associated with reduced viral shedding in human challenge studies but do not independently predict disease severity .
HA Head Antibodies: Potent neutralizers but limited to specific subtypes (e.g., H1) due to antigenic drift .
NA Antibodies: Synergize with HA-targeting antibodies; FNI9’s Fc-independent activity suggests therapeutic potential even in late-stage infection .
HUA1 is involved in flower development. It functions in floral reproductive organ identity determination by binding to and promoting the processing of AGAMOUS (AG) pre-messenger RNA (pre-mRNA). This activity occurs in association with HUA2 and HEN4 proteins.