Target intelligence / Profile preview

Human cytomegalovirus antigen-Hepatitis B virus-like particle vaccine (HCMV-HBV VLP)

Target
HCMV-HBV VLP
Molecular classification
Vaccine, Virus-like particle, Recombinant protein complex
01

Overview

This construct represents a modular vaccine candidate designed to elicit a robust immune response against Human Cytomegalovirus (HCMV). It consists of HCMV antigens, most commonly the glycoprotein B (gB) or the pentameric complex, which are covalently attached to Hepatitis B virus-like particles (HBV VLPs) using the SpyTag/SpyCatcher conjugation system (Janitzek et al., 2016, Vaccine). The SpyTag/SpyCatcher technology allows for the high-density, oriented display of complex antigens on the VLP surface, which mimics the repetitive structure of natural viruses and significantly enhances immunogenicity compared to soluble protein subunits (Thrane et al., 2016, J Nanobiotechnol). By presenting HCMV antigens in this multivalent format, the vaccine candidate aims to induce high titers of neutralizing antibodies and activate cellular immune pathways to prevent HCMV infection and its associated complications, such as congenital CMV and disease in transplant recipients. While the HBV VLP serves as an effective scaffold, the primary therapeutic focus is the generation of protective immunity against the HCMV virus itself. This approach represents a significant advancement in vaccine design, combining the safety of subunit vaccines with the potency of particulate delivery systems.

Other names
HCMV gB-VLPSpyTag-SpyCatcher HCMV vaccineVLP-displayed HCMV antigenHCMV gB-HBV VLP
02

Mechanism of action

The construct acts as a vaccine by presenting Human Cytomegalovirus (HCMV) antigens, such as glycoprotein B (gB) or the pentameric complex, in a highly repetitive, multivalent format on the surface of Hepatitis B virus-like particles (HBV VLPs). This arrangement mimics the structure of a native virus, which facilitates the cross-linking of B-cell receptors and enhances the induction of high-titer neutralizing antibodies and cellular immune responses (Janitzek et al., 2016, Vaccine; Thrane et al., 2016, J Nanobiotechnol).

03

Biological functions

Immune response inductionAntigen presentationB-cell receptor cross-linking
04

Disease associations

Human cytomegalovirus infectionCongenital CMV infection
05

Safety considerations

Injection site reactionsPotential for anti-scaffold (HBV) immune interferenceSystemic immunogenicity
06

Biomarkers

Anti-HCMV IgG antibody titerNeutralizing antibody titerHCMV viral load

Beyond the preview

Go deeper on Human cytomegalovirus antigen-Hepatitis B virus-like particle vaccine (HCMV-HBV VLP).

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Drug pipeline

Full profile access

Explore the programs pursuing this target and their development progress.

  • Drug candidates
  • Developers
  • Development stage

Clinical trials

Full profile access

Follow the clinical studies evaluating therapies directed at this target.

  • Trial design
  • Status
  • Readouts

Competitive landscape

Full profile access

Compare approaches across drug candidates, modalities, and indications.

  • Programs
  • Modalities
  • Indications

Literature & evidence

Full profile access

Investigate the research and source evidence behind target biology and development.

  • Publications
  • Sources
  • Analysis

Patents

Full profile access

Explore patent activity around therapies and technologies addressing this target.

  • Patents
  • Assignees
  • Technologies

Research & analysis

Full profile access

Connect target biology, drug development, and emerging evidence in your research.

  • Biology
  • Development news
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on Human cytomegalovirus antigen-Hepatitis B virus-like particle vaccine (HCMV-HBV VLP).

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call