Creative Biolabs provides a series of Influenza B Virus antibody products and services to meet the various needs of researchers. Our offerings include:
Our solutions deliver the tools and expertise necessary to overcome the obstacles in Influenza B Virus research.
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Influenza B virus (IBV), Orthomyxoviridae member, persists as a clinically consequential agent of seasonal respiratory pathology, disproportionately impacting pediatric and geriatric cohorts despite lacking zoonotic reservoirs. Its eight-segment, negative-sense RNA genome encodes the canonical HA/NA glycoprotein dyad, with HA’s α2,6-linked sialic acid tropism dictating upper respiratory tract epithelial tropism—a niche fidelity distinguishing it from broader-tissue-tropic influenza A variants. IBV replication is choreographed through HA-mediated clathrin-dependent endocytosis, pH-dependent endosomal fusion, and nuclear import of viral ribonucleoprotein (vRNP) complexes.
Fig. 1 Overview of influenza B genome and proteins.1
Notably, IBV’s evolutionary epidemiology is constrained by its limited host range, resulting in slower antigenic drift (∼2.3 substitutions/year in HA1) compared to influenza A. Current research dissects its immune evasion stratagems, including NS1-mediated blockade of RIG-I/MAVS signaling and PB1-F2-driven mitochondrial ROS amplification—mechanisms that dysregulate IFN-λ production in ciliated epithelial cells. Paradoxically, IBV’s reduced adaptive plasticity enhances vulnerability to broadly neutralizing antibodies (bnAbs) targeting HA’s conserved vestigial esterase domain, a vulnerability now being exploited in pan-IBV vaccine design.
Antibodies directed against influenza B virus (IBV) surface antigens—notably the hemagglutinin (HA) stalk domain and neuraminidase (NA) catalytic pocket—orchestrate both seroconversion-mediated immunity and vaccine-derived protection through dual mechanisms: steric hindrance of receptor avidity and Fc-effector recruitment. Recent breakthroughs in humoral immunology have yielded mAbs with pan-IBV efficacy, exemplified by the BDA-11 mAb targeting HA’s fusion peptide-proximal hydrophobic groove, which neutralizes all IBV lineages with picomolar potency and confers cross-protection in ferret challenge models.
Structural virology studies reveal that broadly neutralizing mAbs engage quaternary epitopes spanning HA1-HA2 interfaces or NA’s conserved enzymatic cleft, leveraging heterosubtypic breadth through glycan-shield penetration or sialic acid mimetic strategies. These mAbs synergistically activate alveolar macrophage phagocytosis via FcγRIIIa engagement while blocking HA’s pH-dependent conformational rearrangements, as evidenced by cryo-EM reconstructions of HA–Fab complexes.
Creative Biolabs tries its best to provide you with exceptional products and services. Our Influenza B Virus antibody solutions stand out due to:
A1: Yes, Creative Biolabs offers customized antibody solutions to meet your unique research needs. We provide comprehensive custom antibody development services.
A2: Creative Biolabs complies with strict quality control standards during the whole production process. Also, our antibodies products have been validated and characterized.
A3: Please refer to the specific datasheet for detailed handling instructions. In general, antibodies should be stored at the recommended conditions to maintain their activity and avoid repeated freeze-thaw cycles.
For more information about Creative Biolabs' Influenza B Virus antibodies and services, please contact us.
REFERENCE
Anti-IBV Neutralizing Antibody (V3S-0622-YC294) (CAT#: V3S-0622-YC294)
Target: IBV
Host Species: Human
Target Species: Influenza B virus (IBV),
Application: ELISA,Neut,FuncS,