Target intelligence / Profile preview

Glycoprotein B (herpesvirus) (gB)

Target
gB
Molecular classification
Viral envelope glycoprotein, Class III viral fusogen, Viral fusion protein, Other
01

Overview

Glycoprotein B (gB) is an essential envelope protein found in all herpesviruses, including human cytomegalovirus (HCMV), herpes simplex virus (HSV), and Epstein-Barr virus (EBV). As a class III viral fusion protein, gB mediates the fusion of the viral envelope with host cell membranes, a critical step for viral entry and cell-to-cell spread[1][2][6][8][9]. gB elicits strong immune responses and is a major target of neutralizing antibodies, but the majority of the antibody response is non-neutralizing due to extensive glycosylation that shields key neutralizing epitopes[1][3][4][5][8]. It also induces innate immune signaling, interacts with cellular receptors (e.g., Toll-like receptor 2, integrins), and is involved in viral maturation and egress[2][6][9]. gB has been used as a vaccine antigen (e.g., gB/MF59 in HCMV), but challenges remain due to immune evasion mechanisms. Its structure has been elucidated and reveals complex domain organization relevant for therapeutic and vaccine design[1][3][4][5][8].

Other names
HCMV glycoprotein BHuman cytomegalovirus glycoprotein BHSV glycoprotein B (for herpes simplex variants)EBV glycoprotein B (for Epstein-Barr virus variants)UL55 (HCMV gene name)Herpesvirus gB
02

Mechanism of action

Antibody-mediated neutralization of viral entry/fusion; Fusion inhibition: blocking viral fusion with host cell membranes; Interference with immune evasion through neutralizing/non-neutralizing epitope targeting

03

Biological functions

Membrane fusion (virus-cell and cell-cell fusion)Viral entry into host cellsInduction of host immune response, including neutralizing antibody productionActivation of innate immune responses (e.g., interferon)Induction of cellular signaling, including cytokine production and cytoskeletal rearrangements
04

Disease associations

Infection (essential for herpesvirus infectivity, especially cytomegalovirus, herpes simplex virus, and Epstein-Barr virus)Congenital infection (HCMV)Immunocompromised host disease (HCMV in transplant, HIV patients)Other (associated with viral latency, dissemination, and pathogenesis)
05

Safety considerations

Immune evasion: gB glycosylation may shield neutralizing epitopes, reducing vaccine effectivenessLimited neutralizing antibody response in natural infection; most anti-gB antibodies are non-neutralizingPotential for antibody-dependent enhancement is theoretical but not established
06

Interacting drugs

None are FDA-approved for direct gB targeting, but: Vaccine-derived antibodies (e.g., gB/MF59 vaccine for HCMV induces anti-gB antibodies)

2 more in the full profile.

07

Biomarkers

Presence of anti-gB antibodies as a marker of infection and immune responsegB antigenemia in CMV diagnostic assays (clinical virology)

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