Langerin, the "Catcher in the Rye": an important receptor for pathogens on Langerhans cells

Patrizia Stoitzner1, Nikolaus Romani

  • 1Department of Dermatology & Venereology, Innsbruck Medical University, Innsbruck, Austria. patrizia.stoitzner@i-med.ac.at

Insights

Langerin on human Langerhans cells binds measles virus but does not cause infection or cross-presentation. This receptor is crucial for presenting measles virus to CD4+ T cells, impacting antiviral immunity.

Area of Science:

  • Immunology
  • Dermatology
  • Virology

Background:

  • Langerhans cells (LCs) are key antigen-presenting cells in the skin's epidermis.
  • LCs utilize C-type lectin receptors, like Langerin/CD207, for pathogen uptake.
  • Understanding LC interactions with viruses is vital for antiviral immunity and immunotherapy.

Purpose of the Study:

  • To investigate the role of Langerin on human LCs in measles virus interaction.
  • To determine if Langerin mediates measles virus capture, infection, and T-cell presentation.
  • To elucidate the specific T-cell responses induced by measles virus-LC interactions.

Main Methods:

  • Analysis of human Langerhans cells and measles virus.
  • Assessment of virus binding, capture, and infection mediated by Langerin.
  • Evaluation of T-cell activation, including CD4+ and CD8+ T cells, following virus exposure.

Main Results:

  • Langerin facilitates the binding and capture of measles virus by human LCs.
  • Measles virus does not productively infect LCs via Langerin.
  • LCs present measles virus to CD4+ T cells in a Langerin-dependent manner, but not to CD8+ T cells (cross-presentation).

Conclusions:

  • Langerin's primary role in LCs concerning measles virus is pathogen capture for CD4+ T-cell priming, not productive infection or cross-presentation.
  • Cross-presentation of measles virus may be mediated by other skin dendritic cell subsets.
  • These findings underscore the intricate nature of skin-initiated antiviral T-cell responses and highlight the potential of human skin dendritic cells in immunotherapy.

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