Human papillomavirus virus-like particles do not activate Langerhans cells: a possible immune escape mechanism used by human papillomaviruses

J Immunol. 2002 Sep 15;169(6):3242-9. doi: 10.4049/jimmunol.169.6.3242.

Abstract

High-risk human papillomaviruses are linked to several malignancies including cervical cancer. Because human papillomavirus-infected women do not always mount protective antiviral immunity, we explored the interaction of human papillomavirus with Langerhans cells, which would be the first APCs the virus comes into contact with during infection. We determined that dendritic cells, normally targeted by vaccination procedures and Langerhans cells, normally targeted by the natural virus equally internalize human papillomavirus virus-like particles. However, in contrast to dendritic cells, Langerhans cells are not activated by human papillomavirus virus-like particles, illustrated by the lack of: up-regulating activation markers, secreting IL-12, stimulating T cells in an MLR, inducing human papillomavirus-specific immunity, and migrating from epidermal tissue. Langerhans cells, like dendritic cells, can display all of these characteristics when stimulated by proinflammatory agents. These data may define an intriguing immune escape mechanism used by human papillomavirus and form the basis for designing optimal vaccination strategies.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antigens, CD / biosynthesis
  • Cell Differentiation / immunology
  • Cell Movement / immunology
  • Cells, Cultured
  • Dendritic Cells / immunology
  • Dendritic Cells / metabolism
  • Dendritic Cells / ultrastructure
  • Dendritic Cells / virology
  • Epidermal Cells
  • Epidermis / immunology
  • Epidermis / virology
  • Epitopes, T-Lymphocyte / immunology
  • Female
  • Humans
  • Interleukin-12 / metabolism
  • Langerhans Cells / immunology*
  • Langerhans Cells / metabolism
  • Langerhans Cells / ultrastructure
  • Langerhans Cells / virology*
  • Lymphocyte Activation
  • Mice
  • Mice, Inbred C57BL
  • Monocytes / immunology
  • Monocytes / metabolism
  • Monocytes / ultrastructure
  • Monocytes / virology
  • Organ Culture Techniques
  • Papillomaviridae / genetics
  • Papillomaviridae / immunology*
  • Papillomaviridae / metabolism
  • Papillomaviridae / ultrastructure
  • Phagocytosis / immunology
  • Protein Subunits
  • Recombinant Fusion Proteins / immunology
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / virology
  • Up-Regulation / immunology
  • Virion / genetics
  • Virion / immunology*
  • Virion / metabolism
  • Virion / ultrastructure

Substances

  • Antigens, CD
  • Epitopes, T-Lymphocyte
  • Protein Subunits
  • Recombinant Fusion Proteins
  • Interleukin-12