Vaccine value profile for herpes simplex virus

Christine Johnston*, Suzanne Scheele, Laura Bachmann, Marie-Claude Boily, Nathorn Chaiyakunapruk, Carolyn Deal, Sinead Delany-Moretlwe, Shaun Wen Huey Lee, Katharine J Looker, Caroline Marshall, Maeve Mello, Francis Ndowa, Sami L Gottlieb

*Corresponding author for this work

Research output: Contribution to journalReview article (Academic Journal)peer-review

1 Citation (Scopus)

Abstract

Herpes simplex virus type 1 (HSV-1) and type 2 (HSV-2) are chronic, highly prevalent viral infections that cause significant morbidity around the world. HSV-2 is sexually transmitted and is the leading cause of genital ulcer disease (GUD). It also increases the risk of HIV acquisition, fueling the HIV epidemic. HSV-1 is typically acquired in childhood through nonsexual contact and contributes to oral and ocular disease, but it can also be sexually transmitted to cause GUD. Both HSV-1 and HSV-2 cause neonatal herpes and neurologic disease. Given the ubiquitous nature of HSV-1 and HSV-2 infections and the limited existing prevention and control measures, vaccination would be the most efficient strategy to reduce the global burden of morbidity related to HSV infection. Vaccine strategies include prophylactic vaccination, which would prevent infection among susceptible persons and would likely be given to adolescents, and therapeutic vaccinations, which would be given to people with symptomatic genital HSV-2 infection. This document discusses the vaccine value profile of both types of vaccines. This 'Vaccine Value Profile' (VVP) for HSV is intended to provide a high-level, holistic assessment of the information and data that are currently available to inform the potential public health, economic and societal value of pipeline vaccines and vaccine-like products. This VVP was developed by subject matter experts from academia, non-profit organizations, government agencies and multi-lateral organizations. All contributors have extensive expertise on various elements of the HSV VVP and collectively aimed to identify current research and knowledge gaps. The VVP was developed using only existing and publicly available information.

Original languageEnglish
Pages (from-to)S82-S100
Number of pages19
JournalVaccine
Volume42
Issue number19
Early online date24 May 2024
DOIs
Publication statusPublished - 25 Jul 2024

Bibliographical note

Publisher Copyright:
© 2024 The Authors

Keywords

  • Humans
  • Herpesvirus 2, Human/immunology
  • Herpes Simplex Virus Vaccines/immunology
  • Herpes Genitalis/prevention & control
  • Herpes Simplex/prevention & control
  • Herpesvirus 1, Human/immunology
  • Vaccination

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