Target intelligence / Profile preview

Varicella-zoster virus glycoproteins and structural proteins (VZV glycoproteins)

Target
VZV glycoproteins
Molecular classification
Viral protein, Glycoprotein, Structural protein, Antigen
01

Overview

Varicella-zoster virus (VZV) glycoproteins and structural proteins are essential components of the Human Herpesvirus 3 virion, playing pivotal roles in the viral life cycle and pathogenesis (Source: PubMed, PMID: 25231300). The glycoproteins, including gE, gB, gH, and gL, are embedded in the viral envelope and mediate critical processes such as attachment to host cells, membrane fusion, and efficient cell-to-cell spread (Source: UniProt, P09258). Structural proteins, including those in the capsid and tegument, facilitate viral assembly and the transport of the viral genome to the nucleus (Source: PubMed, PMID: 19710391). These proteins are central to the pathogenesis of both primary varicella (chickenpox) and the reactivation of latent virus as herpes zoster (shingles) (Source: StatPearls, NBK448139). These proteins are the primary targets for both active immunization and passive immunization strategies. Glycoprotein E (gE) is the most abundant surface protein and serves as the primary antigen in modern recombinant vaccines like Shingrix due to its high immunogenicity (Source: CDC, 2023). Vaccines and immunoglobulins targeting these structural components aim to elicit or provide neutralizing antibodies and T-cell responses to prevent infection and reactivation (Source: NIH, 2022). Consequently, these proteins are fundamental to the clinical management and prevention of VZV-related diseases and their complications, such as postherpetic neuralgia (Source: PubMed, PMID: 29661577).

Other names
VZV envelope glycoproteinsHuman herpesvirus 3 structural proteinsVZV gE/gI complexVZV gBVZV gH/gL complexVZV tegument proteins
02

Mechanism of action

These proteins serve as the primary antigenic targets for vaccines and immunoglobulins; vaccines induce the production of neutralizing antibodies and activate VZV-specific CD4+ T-cells to prevent viral entry and cell-to-cell spread, while immunoglobulins provide immediate passive immunity by binding to surface glycoproteins and neutralizing the virus (Source: PubMed, PMID: 29661577; FDA, VariZIG Label).

03

Biological functions

Viral entryMembrane fusionViral assemblyCell-to-cell spreadImmune evasion (Source: UniProt, P09258)
04

Disease associations

InfectionChickenpoxShinglesPostherpetic neuralgiaVZV vasculopathy (Source: PubMed, PMID: 25231300)
05

Safety considerations

Injection site reactions such as pain, redness, and swelling (Source: CDC, 2023)Systemic reactions including fatigue, myalgia, and headache (Source: FDA, Shingrix Label)Risk of vaccine-derived infection in immunocompromised individuals for live-attenuated vaccines (Source: CDC, 2023)Rare association with Guillain-Barré syndrome following recombinant zoster vaccination (Source: FDA, 2021)
06

Interacting drugs

Varicella Virus Vaccine Live (Varivax)

3 more in the full profile.

07

Biomarkers

VZV-specific IgG antibody titers (Source: Mayo Clinic Laboratories)VZV-specific T-cell frequency via IFN-gamma ELISPOT (Source: PubMed, PMID: 30125529)Detection of VZV DNA by PCR (Source: CDC, 2023)

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