Potential Effects of Human Papillomavirus Type Substitution, Superinfection Exclusion and Latency on the Efficacy of the Current L1 Prophylactic Vaccines

Viruses. 2020 Dec 24;13(1):22. doi: 10.3390/v13010022.

Abstract

There are >200 different types of human papilloma virus (HPV) of which >51 infect genital epithelium, with the ~14 of these classed as high-risk being more commonly associated with cervical cancer. During development of the disease, high-risk types have an increased tendency to develop a truncated non-replicative life cycle, whereas low-risk, non-cancer-associated HPV types are either asymptomatic or cause benign lesions completing their full replicative life cycle. HPVs can also be present as non-replicative so-called "latent" infections and they can also show superinfection exclusion, where cells with pre-existing infections with one type cannot be infected with a different HPV type. Thus, the HPV repertoire and replication status present in an individual can form a complex dynamic meta-community which changes with respect to both time and exposure to different HPV types. In light of these considerations, it is not clear how current prophylactic HPV vaccines will affect this system and the potential for iatrogenic outcomes is discussed in light of recent outcome data.

Keywords: CIN; HPV; L1; latency; prophylactic vaccine; superinfection exclusion; type replacement.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Capsid Proteins / immunology*
  • Female
  • Humans
  • Incidence
  • Neoplasms / etiology
  • Oncogene Proteins, Viral / immunology*
  • Papillomaviridae / classification
  • Papillomaviridae / physiology*
  • Papillomavirus Infections / complications
  • Papillomavirus Infections / pathology
  • Papillomavirus Infections / prevention & control*
  • Papillomavirus Infections / virology
  • Papillomavirus Vaccines / immunology*
  • Prevalence
  • Squamous Intraepithelial Lesions of the Cervix / etiology
  • Squamous Intraepithelial Lesions of the Cervix / pathology
  • Superinfection / virology*
  • Vaccination
  • Virus Latency* / immunology
  • Virus Replication

Substances

  • Capsid Proteins
  • HPV L1 protein, Human papillomavirus
  • Oncogene Proteins, Viral
  • Papillomavirus Vaccines