Journal article : Review
Progress and prospects for herpesvirus vaccination using gB antigens
- Abstract:
- The success of vaccines against varicella zoster virus (VZV) demonstrates the feasibility of high-level efficacy against clinical consequences of herpesvirus infection, but there is a need for new vaccines against others – in particular Epstein-Barr Virus (EBV), human cytomegalovirus (HCMV) and herpes simplex virus 1 and 2 (HSV). Herpesviruses use surface glycoproteins to trigger membrane fusion during cell invasion. Glycoprotein B (gB) is conserved across the family and acts as the fusogen. Vaccines based upon viral fusion proteins protect against many other viruses, and a gB-targeting HCMV vaccine achieved partial efficacy in clinical trials. This experience encourages development of improved gB-based antigens and formulations. There has recently been progress in stabilisation of the pre-fusion conformation of gB, which may be the more relevant structure with respect to immunological protection. Nonetheless gB-targeting vaccines have received less attention recently than vaccines against receptor-binding glycoproteins such as EBV gH/gL and gp350, and HCMV pentamer. We therefore seek to review current knowledge regarding gB as a vaccine antigen: understanding of herpesvirus gB structure and function, within the context of the wider process of herpesvirus entry into host cells; insights relevant to vaccine development from in vitro studies of antibody-gB interactions and effects; and the results from previous in vivo studies using gB-based vaccines. We conclude by critically appraising the potential for gB antigens to contribute to future herpesvirus vaccines, as compared to alternative or complementary approaches.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Version of record, pdf, 36.1MB, Terms of use)
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- Publisher copy:
- 10.3389/fimmu.2026.1827628
Authors
- Publisher:
- Frontiers Media
- Journal:
- Frontiers in Immunology More from this journal
- Volume:
- 17
- Pages:
- 1827628
- Article number:
- 1827628
- Publication date:
- 2026-05-29
- Acceptance date:
- 2026-05-15
- DOI:
- EISSN:
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1664-3224
- ISSN:
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1664-3224
- Language:
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English
- Keywords:
- Subtype:
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Review
- Source identifiers:
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4225545
- Deposit date:
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2026-06-12
- ARK identifier:
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Terms of use
- Copyright date:
- 2026
- Licence:
- CC Attribution (CC BY)
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