Immune evasion in human papillomavirus-associated cervical cancer

Nat Rev Cancer. 2002 Jan;2(1):59-65. doi: 10.1038/nrc700.

Abstract

Tumour-associated viruses produce antigens that, on the face of it, are ideal targets for immunotherapy. Unfortunately, these viruses are experts at avoiding or subverting the host immune response. Cervical-cancer-associated human papillomavirus (HPV) has a battery of immune-evasion mechanisms at its disposal that could confound attempts at HPV-directed immunotherapy. Other virally associated human cancers might prove similarly refractive to immuno-intervention unless we learn how to circumvent their strategies for immune evasion.

Publication types

  • Review

MeSH terms

  • Animals
  • Antigen Presentation
  • Antigen-Presenting Cells / immunology
  • Antigens, Viral / immunology
  • Capsid / immunology
  • Cell Transformation, Viral
  • Codon / genetics
  • Dendritic Cells / immunology
  • Female
  • Gene Expression Regulation, Viral
  • Genetic Code
  • Humans
  • Immune Tolerance
  • Immunologic Surveillance
  • Interferons / physiology
  • Keratinocytes / virology
  • Mice
  • Mice, Transgenic
  • Molecular Mimicry
  • Oncogene Proteins, Viral / immunology
  • Oncogene Proteins, Viral / physiology
  • Papillomaviridae / genetics
  • Papillomaviridae / immunology*
  • Papillomavirus Infections / immunology*
  • Uterine Cervical Neoplasms / immunology*
  • Uterine Cervical Neoplasms / virology
  • Viral Proteins / genetics
  • Viral Proteins / immunology
  • Viral Proteins / physiology

Substances

  • Antigens, Viral
  • Codon
  • Oncogene Proteins, Viral
  • Viral Proteins
  • Interferons