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Human cytomegalovirus envelope glycoprotein (primarily glycoprotein B, gB, plus related viral surface proteins) (CMV gB (for glycoprotein B); others do not have standardized abbreviations)

Target
CMV gB (for glycoprotein B); others do not have standardized abbreviations
Molecular classification
Viral surface glycoprotein, Viral fusion protein, MHC-I-like immunoevasins
01

Overview

The CMV viral surface antigens are a group of proteins exposed on the outer lipid envelope of human cytomegalovirus. The primary antigen, glycoprotein B (gB), is a class III viral fusion protein essential for viral entry, and serves as the major immunogenic determinant for neutralizing antibody responses. Other key antigens include the trimeric (gH/gL/gO) and pentameric (gH/gL/UL128/UL130/UL131) glycoprotein complexes, which mediate host cell recognition and entry. In addition, CMV encodes MHC-I-like molecules that contribute to immune evasion by interfering with host natural killer and cytotoxic T-cell responses. These surface antigens are central to vaccine development and antibody-based therapeutics but present unique challenges due to extensive glycosylation, immunoevasive strategies, and the predominance of non-neutralizing antibody responses. They play a critical role in CMV pathogenesis, especially in immunocompromised and congenitally infected populations

Other names
Cytomegalovirus envelope glycoproteinsHCMV surface antigensCMV glycoprotein BCMV gBCMV gH/gLCMV pentamer/trimer complexCMV MHC-I-like molecules
02

Mechanism of action

Neutralizing antibodies: Block viral attachment or membrane fusion Vaccine-induced immunity: Induces antibody and T-cell responses

03

Biological functions

Viral entry (membrane fusion, receptor binding)Immune evasion (glycosylation shielding, MHC-I mimicry)Elicitation of immune response (antibody and cellular immunity)
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Disease associations

Infection (Cytomegalovirus disease, congenital CMV, immunocompromised host infections)
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Safety considerations

High antigenic and glycosylation variability reduces vaccine efficacyNon-neutralizing antibody responses often predominatePotential for immune evasion or incomplete protection due to diversity of antigens
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Interacting drugs

Vaccines under development or experimental (e.g., recombinant CMV gB vaccine candidates)

1 more in the full profile.

07

Biomarkers

CMV gB antibody titers (used to assess vaccine efficacy, immune status)Other antigen-specific antibody responses (e.g., to gH/gL complexes)

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