Affiliations 

  • 1 Division of Allergy & Infectious Diseases, University of Washington, Seattle, WA, USA. Electronic address: cjohnsto@uw.edu
  • 2 Center for Vaccine Introduction and Access, PATH, Washington, DC, USA
  • 3 Division of STD Prevention, Centers for Disease Control and Prevention, Atlanta, GA, USA
  • 4 MRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, UK
  • 5 Department of Pharmacotherapy, University of Utah College of Pharmacy, Salt Lake City, UT, USA
  • 6 Enteric and Sexually Transmitted Diseases Branch, National Institute of Allergy and Infectious Diseases, Bethesda, MD, USA
  • 7 Wits RHI, Johannesburg, South Africa
  • 8 Monash University Malaysia, Subang, Malaysia
  • 9 Population Health Sciences, Bristol Medical School, University of Bristol, UK
  • 10 Department of Immunizations, Vaccines and Biologicals, World Health Organization, Geneva, Switzerland
  • 11 Global HIV, Hepatitis and STI Programmes, World Health Organization, Geneva, Switzerland
  • 12 Skin and GU Medicine Clinic, Harare, Zimbabwe
  • 13 Department of Sexual and Reproductive Health and Research, World Health Organization, Geneva, Switzerland
Vaccine, 2024 Jul 25;42(19S1):S82-S100.
PMID: 39003018 DOI: 10.1016/j.vaccine.2024.01.044

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.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.